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array:23 [ "pii" => "S0214916823000906" "issn" => "02149168" "doi" => "10.1016/j.arteri.2023.10.001" "estado" => "S300" "fechaPublicacion" => "2024-03-01" "aid" => "690" "copyright" => "Sociedad Española de Arteriosclerosis" "copyrightAnyo" => "2023" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Clin Invest Arterioscl. 2024;36:60-70" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "itemSiguiente" => array:19 [ "pii" => "S0214916823001158" "issn" => "02149168" "doi" => "10.1016/j.arteri.2023.11.005" "estado" => "S300" "fechaPublicacion" => "2024-03-01" "aid" => "697" "copyright" => "Sociedad Española de Arteriosclerosis" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Clin Invest Arterioscl. 2024;36:71-7" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "es" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">ORIGINAL</span>" "titulo" => "Influencia de la concentración de triglicéridos en la lipoproteína(a) en función de la dislipidemia" "tienePdf" => "es" "tieneTextoCompleto" => "es" "tieneResumen" => array:2 [ 0 => "es" 1 => "en" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "71" "paginaFinal" => "77" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Influence of triglyceride concentration in lipoprotein (a) as a function of dyslipidemia" ] ] "contieneResumen" => array:2 [ "es" => true "en" => true ] "contieneTextoCompleto" => array:1 [ "es" => true ] "contienePdf" => array:1 [ "es" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figura 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 1033 "Ancho" => 1675 "Tamanyo" => 108542 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Concentración de Lp(a) en la población total del Registro de Dislipemias dividida por grupos de TG y separada por la presencia de HF.</p> <p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">HF: hipercolesterolemia familiar; Lp(a): lipoproteína(a); TG: triglicéridos.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Victoria Marco-Benedí, Ana Cenarro, Martín Laclaustra, Pilar Calmarza, Ana M. Bea, Àlex Vila, Carlos Morillas-Ariño, José Puzo, Juan Diego Mediavilla Garcia, Amalia Inmaculada Fernández Alamán, Manuel Suárez Tembra, Fernando Civeira" "autores" => array:12 [ 0 => array:2 [ "nombre" => "Victoria" "apellidos" => "Marco-Benedí" ] 1 => array:2 [ "nombre" => "Ana" "apellidos" => "Cenarro" ] 2 => array:2 [ "nombre" => "Martín" "apellidos" => "Laclaustra" ] 3 => array:2 [ "nombre" => "Pilar" "apellidos" => "Calmarza" ] 4 => array:2 [ "nombre" => "Ana M." "apellidos" => "Bea" ] 5 => array:2 [ "nombre" => "Àlex" "apellidos" => "Vila" ] 6 => array:2 [ "nombre" => "Carlos" "apellidos" => "Morillas-Ariño" ] 7 => array:2 [ "nombre" => "José" "apellidos" => "Puzo" ] 8 => array:2 [ "nombre" => "Juan Diego" "apellidos" => "Mediavilla Garcia" ] 9 => array:2 [ "nombre" => "Amalia Inmaculada" "apellidos" => "Fernández Alamán" ] 10 => array:2 [ "nombre" => "Manuel" "apellidos" => "Suárez Tembra" ] 11 => array:2 [ "nombre" => "Fernando" "apellidos" => "Civeira" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S2529912324000147" "doi" => "10.1016/j.artere.2024.03.001" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2529912324000147?idApp=UINPBA00004N" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0214916823001158?idApp=UINPBA00004N" "url" => "/02149168/0000003600000002/v1_202403080539/S0214916823001158/v1_202403080539/es/main.assets" ] "itemAnterior" => array:18 [ "pii" => "S0214916823000876" "issn" => "02149168" "doi" => "10.1016/j.arteri.2023.09.002" "estado" => "S300" "fechaPublicacion" => "2024-03-01" "aid" => "689" "copyright" => "Sociedad Española de Arteriosclerosis" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Clin Invest Arterioscl. 2024;36:51-9" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "en" => array:12 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original article</span>" "titulo" => "Evaluation of the relationship between atherosclerosis and <span class="elsevierStyleItalic">Helicobacter pylori</span> infection with measurement of growth differentiation factor 15 and atherosclerosis indicators in adults with no comorbidity" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "51" "paginaFinal" => "59" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Evaluación de la relación entre aterosclerosis e infección por <span class="elsevierStyleItalic">Helicobacter pylori</span> con medición del factor de diferenciación de crecimiento 15 e indicadores de aterosclerosis en adultos sin comorbilidad" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Osman Başpinar, Ayça Elibol, Derya Koçer, Turgut Tursem Tokmak, Serkan Doğan, Oğuzhan Sıtkı Dizdar" "autores" => array:6 [ 0 => array:2 [ "nombre" => "Osman" "apellidos" => "Başpinar" ] 1 => array:2 [ "nombre" => "Ayça" "apellidos" => "Elibol" ] 2 => array:2 [ "nombre" => "Derya" "apellidos" => "Koçer" ] 3 => array:2 [ "nombre" => "Turgut Tursem" "apellidos" => "Tokmak" ] 4 => array:2 [ "nombre" => "Serkan" "apellidos" => "Doğan" ] 5 => array:2 [ "nombre" => "Oğuzhan Sıtkı" "apellidos" => "Dizdar" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0214916823000876?idApp=UINPBA00004N" "url" => "/02149168/0000003600000002/v1_202403080539/S0214916823000876/v1_202403080539/en/main.assets" ] "en" => array:20 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Original article</span>" "titulo" => "High-fat diet promotes coagulation and endothelial activation in Sprague Dawley rats: Short-term effects of combined oral contraceptives" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "60" "paginaFinal" => "70" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Oyesanmi A. Fabunmi, Phiwayinkosi V. Dludla, Bongani B. Nkambule" "autores" => array:3 [ 0 => array:3 [ "nombre" => "Oyesanmi A." "apellidos" => "Fabunmi" "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 1 => array:3 [ "nombre" => "Phiwayinkosi V." "apellidos" => "Dludla" "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">d</span>" "identificador" => "aff0020" ] ] ] 2 => array:4 [ "nombre" => "Bongani B." "apellidos" => "Nkambule" "email" => array:1 [ 0 => "Nkambuleb@ukzn.ac.za" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] ] "afiliaciones" => array:4 [ 0 => array:3 [ "entidad" => "School of Laboratory Medicine and Medical Sciences (SLMMS), College of Health Sciences, University of KwaZulu-Natal, Durban 4000, South Africa" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Department of Physiology, College of Medicine, Ekiti State University, Ado-Ekiti 5363, Nigeria" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Cochrane South Africa, South African Medical Research Council, Tygerberg 7505, South Africa" "etiqueta" => "c" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "Department of Biochemistry and Microbiology, University of Zululand, KwaDlangezwa 3880, South Africa" "etiqueta" => "d" "identificador" => "aff0020" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Dieta alta en grasas promueve la coagulación y la activación endotelial en ratas Sprague Dawley: efectos a corto plazo de los anticonceptivos orales combinados" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0020" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 769 "Ancho" => 1508 "Tamanyo" => 85296 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Effect of combined oral contraceptive treatment on biomarkers of coagulation cascade like tissue factor (A) and D-dimer (B). All results are presented as mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>SEM. Significance indicated between LFD and HFD<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>high dose COC. *<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05; **<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001. Key: LFD: low fat diet; HFD: high fat diet; COC: combined oral contraceptive.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Cardiovascular disease (CVD) account for at least a third of the mortality occurring in low and middle-income countries (LMIC).<a class="elsevierStyleCrossRefs" href="#bib0380"><span class="elsevierStyleSup">1,2</span></a> Despite the advancements in the therapeutics and management of patients with chronic disease,<a class="elsevierStyleCrossRef" href="#bib0390"><span class="elsevierStyleSup">3</span></a> CVD still account for a substantial number of deaths in people living with metabolic complications.<a class="elsevierStyleCrossRef" href="#bib0395"><span class="elsevierStyleSup">4</span></a> Obesity remains a predominant risk factor for thrombosis which is characterized by increased plasma levels or activity of coagulation factors and fibrinolytic proteins which contribute to major adverse cardiovascular events (MACEs).<a class="elsevierStyleCrossRef" href="#bib0400"><span class="elsevierStyleSup">5</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Of note, the pathological enlargement of the adipose tissue in obesity elicits the release of pro-inflammatory molecules that induce damage to the endothelium.<a class="elsevierStyleCrossRefs" href="#bib0405"><span class="elsevierStyleSup">6,7</span></a> This further results in the altered release of nitric oxide (NO) and negatively affect other vasodilatory metabolites leading to endothelial dysfunction<a class="elsevierStyleCrossRefs" href="#bib0415"><span class="elsevierStyleSup">8,9</span></a> and arterial stiffening.<a class="elsevierStyleCrossRefs" href="#bib0425"><span class="elsevierStyleSup">10,11</span></a> Furthermore, the endothelium may be transformed from an antithrombotic to prothrombotic state in obesity which may orchestrate haemostatic imbalances.<a class="elsevierStyleCrossRefs" href="#bib0435"><span class="elsevierStyleSup">12–14</span></a> During a prothrombotic state, tissue factor (TF), von Willebrand factor (vWF) and P-selectin promote the adhesion of platelet on the endothelium.<a class="elsevierStyleCrossRefs" href="#bib0450"><span class="elsevierStyleSup">15–19</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The use of oral contraceptives especially the combined oral contraceptives (COCs) is a commonly modern method for birth control.<a class="elsevierStyleCrossRefs" href="#bib0475"><span class="elsevierStyleSup">20,21</span></a> However, the use of COC is also associated with endothelial and haemostatic dysregulation which increases the risk of CVD.<a class="elsevierStyleCrossRefs" href="#bib0485"><span class="elsevierStyleSup">22,23</span></a> Some of the established mechanism by which COC impact the vasculature include the activation of aldosterone-mineralocorticoid receptor axis among others.<a class="elsevierStyleCrossRefs" href="#bib0475"><span class="elsevierStyleSup">20,24</span></a> However, findings are inconsistent and others indicate no correlation exist between the use of COC and changes in major makers of endothelial function like NO and endothelin-1 in premenopausal women.<a class="elsevierStyleCrossRef" href="#bib0500"><span class="elsevierStyleSup">25</span></a> In contrast, experimental study suggests that COC treatment may alter endothelial function and haemostasis and ultimately promote inflammation.<a class="elsevierStyleCrossRef" href="#bib0505"><span class="elsevierStyleSup">26</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">Nonetheless, there is a need to continuously assess the impact of hormonal contraceptives for their potential effects in causing vascular dysfunction in women at risk of developing CVD.<a class="elsevierStyleCrossRef" href="#bib0510"><span class="elsevierStyleSup">27</span></a> Beyond providing insight into the pathophysiology of vascular disease in those with metabolic anomalies, this would enhance our understanding on the potential influence of oral contraceptives in driving CVD-risk among susceptible individuals.<a class="elsevierStyleCrossRefs" href="#bib0515"><span class="elsevierStyleSup">28,29</span></a> In the current study, we first assess the impact of high fat diet (HFD) on dysregulating biomarkers of coagulation and endothelial activation in Sprague Dawley rats. We further investigated the influence of COC treatment in these HFD-fed rats.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Materials and methods</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Animal handlings</span><p id="par0025" class="elsevierStylePara elsevierViewall">Twenty (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>20) five-week-old female Sprague Dawley rats weighing between 150 and 200<span class="elsevierStyleHsp" style=""></span>g were used for this study. The animals were purchased and housed at the Biomedical Research Unit (BRU) of the University KwaZulu-Natal (UKZN; South Africa). Animal handling followed guidelines and principles, as published by the Committee for the Care and Use of Laboratory Animals.<a class="elsevierStyleCrossRef" href="#bib0525"><span class="elsevierStyleSup">30</span></a> Briefly the animals acclimatized for 2 weeks before commencement of the study, with an unrestricted access to food and water throughout the project. This was done within an environment-temperature (22<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2<span class="elsevierStyleHsp" style=""></span>°C), humidity (55<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>5%), controlled 12-h light cycle (6:00–18:00) and dark cycle (18:00–6:00). Ethical clearance for this study was granted by the UKZN animal research ethics committee, ethics registration number AREC/00003067/2021.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Study design</span><p id="par0030" class="elsevierStylePara elsevierViewall">The study contained two major experiment phases. The first experiment group comprised of 10 female animals (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>5/group) that were kept on a HFD (containing 20% protein and 60% fat; #D12492) for eight weeks and a control group which was randomized to receive LFD (containing 20% protein and 10% fat; #D12450) (Research Diets, Inc.; New Jersey, United States). The diet composition and duration of HFD-feeding follows previously published literature.<a class="elsevierStyleCrossRef" href="#bib0530"><span class="elsevierStyleSup">31</span></a> The food and water intake were measured weekly via metabolic cages (Techniplats, Labotec, South Africa). Moreover, body weights were monitored weekly while the hemodynamic and haemostatic changes were determined at the last week of the experiment to minimize stress.</p><p id="par0035" class="elsevierStylePara elsevierViewall">The second experimental phase contained 10 rats (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>5/group) that were kept on a HFD for 8 weeks before receiving levonorgestrel-containing oral contraceptives (COC) for 6 weeks,<a class="elsevierStyleCrossRef" href="#bib0535"><span class="elsevierStyleSup">32</span></a> at low dose (4.5<span class="elsevierStyleHsp" style=""></span>μg of levonorgestrel and 0.9<span class="elsevierStyleHsp" style=""></span>μg ethinylestradiol) or high dose (9<span class="elsevierStyleHsp" style=""></span>μg levonorgestrel and 1.8<span class="elsevierStyleHsp" style=""></span>μg ethinylestradiol) (Aspen Pharmacare, South Africa).<a class="elsevierStyleCrossRef" href="#bib0540"><span class="elsevierStyleSup">33</span></a> Additional rats (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>10), exposed to HFD (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>5/group) or LFD (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>5/group) alone, served as controls for diet-induced obesity and experimental control, respectively. Treatments were prepared in distil water.<a class="elsevierStyleCrossRef" href="#bib0545"><span class="elsevierStyleSup">34</span></a> All the treatments were administered daily via oral gavage while the animals were regularly monitored for adverse reaction, and the cages were cleaned daily. After 6 weeks of COC treatment blood samples were drawn from the lateral tail vein into ethylenediaminetetraacetic acid (EDTA) microtainer and vacutainer citrate tubes (BD Bioscience, United States) for further analysis (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>).</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Measurement of hemodynamic variables</span><p id="par0040" class="elsevierStylePara elsevierViewall">Hemodynamic parameters, including {systolic, diastolic, and mean arterial pressure (MAP)} were determined via the tail-cuff method using the non-invasive digital blood pressure (BP) system (BIOPAC System, NTBP250, California, USA). Briefly, the machine has a built-in pump that automatically inflates and deflates the rat tail cuff to provide a linear drop in pressure. The equipment was calibrated each day before measurements and the animals were placed in a restrainer with a cuff attached to a heated tail to allow effective adaptation and habituation. During the day of measurement, the animals were kept warm at ±37<span class="elsevierStyleHsp" style=""></span>°C in an enclosed chamber (IITC Model 303sc Animal Test Chamber, IITC Life Sciences, Woodlands Hills, California, USA) for 15<span class="elsevierStyleHsp" style=""></span>min before blood pressure recording to make the pulsations of the tail artery detectable. All measurements were conducted before mid-day to avoid diurnal variation. The mean arterial pressure was determined as described previously.<a class="elsevierStyleCrossRef" href="#bib0550"><span class="elsevierStyleSup">35</span></a></p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Hemostatic assessment</span><p id="par0045" class="elsevierStylePara elsevierViewall">Hemostatic assessment was determined via the bleeding time which gives an oversight of changes in the primary hemostatic process that occur prior to the clotting phase. Notably, the primary hemostatic phase involves formation of platelet plug during which vWF are released which facilitate platelet adhesiveness to the vascular wall in order to promote stoppage of blood.<a class="elsevierStyleCrossRefs" href="#bib0450"><span class="elsevierStyleSup">15,36</span></a> Thus, the evaluation of both total blood loss and time to cessation of blood flow are important factor to be considered when evaluating effect of certain anti-platelet therapy.<a class="elsevierStyleCrossRef" href="#bib0560"><span class="elsevierStyleSup">37</span></a> Briefly, we assessed the bleeding time in the animals via the tail cut method and this was recorded as previously demonstrated.<a class="elsevierStyleCrossRef" href="#bib0555"><span class="elsevierStyleSup">36</span></a> The tail of the rat was warmed for 1<span class="elsevierStyleHsp" style=""></span>min in water at 40<span class="elsevierStyleHsp" style=""></span>°C and then dried before a small cut was made in the middle of the lower portion of the tail with a scalpel. Bleeding time was recorded when the first drop of blood was collected. Bleeding time was monitored at 30<span class="elsevierStyleHsp" style=""></span>s intervals until bleeding stopped.</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Biochemical analysis</span><p id="par0050" class="elsevierStylePara elsevierViewall">Plasma levels of TF, D-dimer, NO and vWF were determined using an enzyme-linked immunosorbent assay (ELISA) kit (Elabscience Biotechnology Co., Ltd., Houston, Texas, USA). All assays were performed according to the recommended protocol. ELISA used were highly sensitive, and no results were below the detection limits. Briefly, the detection limit were 31.25<span class="elsevierStyleHsp" style=""></span>pg/mL for TF, 78.13<span class="elsevierStyleHsp" style=""></span>ng/mL for D-dimer, 0.16<span class="elsevierStyleHsp" style=""></span>μmol/L for NO and 0.16<span class="elsevierStyleHsp" style=""></span>ng/mL for vWF. The inter-assay coefficient of variation (CV) were <10% for TF, D-dimer, vWF, and 3.7% for NO.</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Statistical analysis</span><p id="par0055" class="elsevierStylePara elsevierViewall">All experimental data were expressed as means<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>standard error of mean (SEM). Normality testing was performed using the Kolmogorov–Smirnov test with Dallal–Wilkinson–Lillie. The mean differences between the LFD and HFD-fed groups were determined using unpaired Student <span class="elsevierStyleItalic">t</span>-test for parametric data and reported as means<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>standard error of mean (SEM). Correlations were performed between MAP, coagulation and endothelia activation markers using Pearson coefficients. Statistical significance for measured variables was determined by one-way (treatment factor) analysis of variance (ANOVA) for the comparison of the mean values of variables among the experimental groups. A post hoc Tukey's multiple comparisons test was performed if the <span class="elsevierStyleItalic">F</span>-value reached statistical significance (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05). All the statistical analysis were performed using the GraphPad Prism version 8.0 software (GraphPad Software Inc., California, USA).</p></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Results</span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Metabolic status of rats fed a high fat diet (HFD) compared to low fat diet (LFD) for 8 weeks</span><p id="par0060" class="elsevierStylePara elsevierViewall">There was a significant decrease in food intake (g/kg/day) in HFD-fed group (37.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.3) when compared with LFD-fed group (51.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.3) (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). Whereas water intake (mL/kg/day) was significantly increased in HFD-fed group (119<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.6) when compared with LFD-fed group (88.1<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.8) (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). Furthermore, HFD-fed rats (289<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.1) showed significant weight gain (g) in comparison to LFD-fed rats (270<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>5.2) (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.002) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). More so, fasting glycemia (mmol/L) was significantly increased in HFD-fed groups (5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.5) when compared with LFD-fed group (3.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.6) (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>0.01) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Hemodynamic profile of LFD and HFD-fed rats for 8 weeks</span><p id="par0065" class="elsevierStylePara elsevierViewall">The systolic and diastolic blood pressure were comparable in both diet groups (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05); however, the MAP (mmHg) was significantly higher in HFD-fed group (107.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.9) when compared to the LFD-fed group (103.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.1) (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>0.03). In addition, the heart rate of both diet groups was comparable (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Haemostatic profile and endothelial markers of LFD and HFD-fed rats for 8 weeks</span><p id="par0070" class="elsevierStylePara elsevierViewall">The bleeding time which was used to determine the haemostatic changes between both diet groups was comparable (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). Furthermore, plasma levels of tissue factor and D-dimer to determine changes in the clotting cascade were also comparable between diet groups (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). In terms of endothelial activation, the plasma levels of Von Willebrand factor were comparable between diet groups (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>A). Whereas the plasma levels of NO were significantly lower in HFD-fed group (8.1<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.5) when compared to LFD-fed group (10<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.3) (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>B).</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Associations between MAP and markers of coagulation cascade and endothelial activation in rats fed HFD for 8 weeks</span><p id="par0075" class="elsevierStylePara elsevierViewall">Next, we determined the relationship that exists between HFD-feeding and the presence of pathological features of atherothrombosis in rats. This was done by assessing if there was any association between MAP and the dysregulation of makers of coagulation and endothelial activation (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>). The result showed that MAP was associated with TF (<span class="elsevierStyleItalic">r</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.97, <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.007) and D-dimer (<span class="elsevierStyleItalic">r</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.87, <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.02) (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>A and B). MAP was also associated with Von Willebrand factor (<span class="elsevierStyleItalic">r</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.88, <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.01) and NO (<span class="elsevierStyleItalic">r</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>−0.86, <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.02) (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>C and D).</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Metabolic status of COC treated HFD-fed rats</span><p id="par0080" class="elsevierStylePara elsevierViewall">The body weights were comparable across experimental groups (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>). However, food intake (<span class="elsevierStyleItalic">F</span><span class="elsevierStyleInf">(3, 16)</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>3.674; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.03) varied across the experimental groups. The post hoc analysis showed a significant decreased food intake in HFD fed rats that received the high dose COC when compared with LFD-fed rats (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>). Meanwhile, water intake was comparable among the groups despite COC treatment group displaying non-significant increase in this parameter (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>). More so, fasting glycemia was comparable across experimental groups (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>).</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Effect of COC on hemodynamic parameters and haemostatic profile in HFD-fed rats</span><p id="par0085" class="elsevierStylePara elsevierViewall">The systolic blood pressure (<span class="elsevierStyleItalic">F</span><span class="elsevierStyleInf">(3, 16)</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>4.390; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.02) differed across the experimental groups. HFD-fed rats receiving high dose COC showed a significant increased systolic blood pressure when compared with the LFD group (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>). While the mean arterial pressure (<span class="elsevierStyleItalic">F</span><span class="elsevierStyleInf">(3, 16)</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>3.4; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.03) also varied across the experimental group, HFD-fed rats receiving high dose COC showed a significant increased mean arterial pressure when compared with the LFD group (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>). Meanwhile, the diastolic blood pressure and heart rate were comparable across all the experimental groups following 6 weeks of COC treatment (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>). Notably, the bleeding time assessment (<span class="elsevierStyleItalic">F</span><span class="elsevierStyleInf">(3, 16)</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>4.390; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.02) also differed across the experimental groups. HFD-fed rats receiving high dose COC showed significant increased bleeding time when compared with the LFD and HFD-fed rats (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>).</p></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Effect COC on biomarkers of coagulation and endothelial activation haemostatic profile in HFD-fed rats</span><p id="par0090" class="elsevierStylePara elsevierViewall">To determine changes in the coagulation cascade, the plasma levels of tissue factor and D-dimer were determined following 6 weeks of COC treatment. Our data showed a varied plasma levels of tissue factor (<span class="elsevierStyleItalic">F</span><span class="elsevierStyleInf">(3, 16)</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>3.862; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.03) and D-dimer (<span class="elsevierStyleItalic">F</span><span class="elsevierStyleInf">(3, 16)</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>5.84; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.007) across the experimental groups respectively. Both tissue factor and D-dimer levels were significantly increased in HFD-fed rats receiving high dose COC when compared with LFD-fed rats (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001) (<a class="elsevierStyleCrossRef" href="#fig0020">Fig. 4</a>A and B). Furthermore, the plasma levels of Von Willebrand factor and NO were measured to determine changes in endothelial activation. Briefly, Willebrand factor (<span class="elsevierStyleItalic">F</span><span class="elsevierStyleInf">(3, 16)</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>3.73; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.03) and NO (<span class="elsevierStyleItalic">F</span><span class="elsevierStyleInf">(3, 16)</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>5.03; <span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>0.01) also differed across the experimental groups respectively. HFD-fed rats receiving high dose COC demonstrated a significant increase in plasma levels of Von Willebrand factor when compared with LFD-fed rats (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05) (<a class="elsevierStyleCrossRef" href="#fig0025">Fig. 5</a>A). Whereas plasma levels of NO are significantly lower in the HFD-fed rats receiving high dose COC when compared with LFD-fed rats (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001) (<a class="elsevierStyleCrossRef" href="#fig0025">Fig. 5</a>B).</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><elsevierMultimedia ident="fig0025"></elsevierMultimedia></span></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0150">Discussion</span><p id="par0095" class="elsevierStylePara elsevierViewall">In this present study we assessed the impact of HFD-feeding on selected biomarkers of coagulation and endothelia activation in HFD-fed rats. Firstly, HFD-feeding for 8-weeks promoted weight gain which was accompanied by alterations in food and water intake when compared with LFD-fed rats (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). Interestingly, such phenotypic changes were similar to previous studies in experimental animals on HFD showing characteristic feature of metabolic syndrome.<a class="elsevierStyleCrossRefs" href="#bib0565"><span class="elsevierStyleSup">38–40</span></a> In fact, our previous study has shown that 8-week HFD-feeding led to the development of metabolic syndrome and increased levels of biomarkers of atherothrombotic disorders and CVD.<a class="elsevierStyleCrossRefs" href="#bib0580"><span class="elsevierStyleSup">41,42</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">In our study, the systolic and diastolic blood pressure including the heart rate were not affected by 8-weeek-treatment with HFD. It is noteworthy that the causal role of dietary fat on hemodynamic changes in animal models of obesity is subject to variation due to the strain of animal.<a class="elsevierStyleCrossRef" href="#bib0565"><span class="elsevierStyleSup">38</span></a> However, evidence from our study corroborates with previous studies where HFD over 10 weeks did not alter the hemodynamic profiles of the animals.<a class="elsevierStyleCrossRefs" href="#bib0590"><span class="elsevierStyleSup">43,38</span></a> Nonetheless, the MAP was significantly higher in HFD-fed rats when compared with LFD-fed rats. This agreed with our results showing that MAP was associated with TF, D-dimer, and NO in these HFD-fed rats.</p><p id="par0105" class="elsevierStylePara elsevierViewall">Furthermore, our results indicated that exposure of rats to HFD for 8-weeks in addition to COC treatment for a 6-week period did not affect the weight gain and fasting glycemia in these the animals, except for food intake, which was significantly reduced in response to a high dose of COC (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>). Although human study showed an association between COC and dyslipidemia.<a class="elsevierStyleCrossRefs" href="#bib0595"><span class="elsevierStyleSup">44–46</span></a> Alterations in the lipid profile levels can be attributed to the lipogenic effect of estrogen in which liver lipogenesis is increased and results in elevated levels of triglycerides and LDL levels. Furthermore, the progestin component of OCs may also increase the hepatic lipase enzyme activity, hence decreasing the serum HDL levels and potentially promoting plague formation during the early stage of atherosclerosis.<a class="elsevierStyleCrossRefs" href="#bib0600"><span class="elsevierStyleSup">45,47</span></a> Our results indicated that COC treatment (especially the high dose) may have a significant role in influencing food intake, sex hormones, and eating behavior in female rats, as previously reported in similar settings.<a class="elsevierStyleCrossRefs" href="#bib0615"><span class="elsevierStyleSup">48–50</span></a> However, the short-term treatment period of 6-weeks in our study may not be sufficient to induce marked changes in HFD-fed rats which depicts the notion of reduced metabolic risk upon short-term COC exposure. Nonetheless, it remained important to determine how COC treatment affected other markers related to the development of CVD.</p><p id="par0110" class="elsevierStylePara elsevierViewall">Noteworthy, treatment of HFD-rats with a high-dose of COC significantly increased the systolic blood and MAP when compared to LFD group. However, such effects occurred without any changes in the hemodynamic profiles, including the diastolic blood pressure and heart rate. While the outcome of our study corroborates previous findings,<a class="elsevierStyleCrossRefs" href="#bib0630"><span class="elsevierStyleSup">51–53</span></a> it also suggested that a dose-dependent relationship between high COC and hemodynamic changes exist. In principle, endogenous female sex hormones are known to be cardioprotective<a class="elsevierStyleCrossRef" href="#bib0645"><span class="elsevierStyleSup">54</span></a> which maybe abrogated during hormonal contraceptive treatment thereby predisposing susceptible individuals to higher risk of MACEs in the presence of several comorbidities such as obesity, smoking and physical inactivity.<a class="elsevierStyleCrossRef" href="#bib0510"><span class="elsevierStyleSup">27</span></a> For instance, the administration of hormone replacement therapy (HRT) in women aged 50–59 years showed a cardioprotective effect by significantly reducing the coronary disease risk factor such coronary artery calcification immediately after menopause. However, HRT was associated with an increased risk of coronary heart disease in women who have been menopausal for 10 or more years and who are older than 60 years.<a class="elsevierStyleCrossRefs" href="#bib0410"><span class="elsevierStyleSup">7,8</span></a></p><p id="par0115" class="elsevierStylePara elsevierViewall">Importantly, beyond assessing the basic metabolic parameters, it remains essential to understand how different doses of COC affects some selected biomarkers of endothelial function in these HFD-rats. Obesity-related complications are multifactorial, and it encompasses alterations to blood flow, hypercoagulability, and endothelial dysfunction which all contribute to the early pathological process of atherothrombotic-CVD.<a class="elsevierStyleCrossRef" href="#bib0650"><span class="elsevierStyleSup">55</span></a> Although eight weeks of HFD-feeding did not alter levels of TF and D-dimer in our study. In contrast, other studies reported changes in the coagulation cascade in HFD-fed mouse model.<a class="elsevierStyleCrossRefs" href="#bib0655"><span class="elsevierStyleSup">56,57</span></a> For instance, female C57Bl/6J mice demonstrated a prothrombotic phenotype after fourteen weeks of HFD-feeding.<a class="elsevierStyleCrossRef" href="#bib0660"><span class="elsevierStyleSup">57</span></a> Cleuren et al. also showed early-onset in procoagulant shift in HFD fed C57BL/6J male mice which persisted during sixteen weeks of HFD-feeding.<a class="elsevierStyleCrossRef" href="#bib0655"><span class="elsevierStyleSup">56</span></a> The physiological difference in the sex and specie of the animals in association with the handling of metabolic stress may contribute to the observed differential change in the coagulation cascade.<a class="elsevierStyleCrossRefs" href="#bib0665"><span class="elsevierStyleSup">58,59</span></a> However, the plasma levels of TF and D-dimer were significantly higher in HFD-fed rats receiving high COC when compared to LFD-fed rats in our study which contrast other previous finding where short-term ethinylestradiol treatment counteracts the prothrombotic phenotype in HFD-fed mice.<a class="elsevierStyleCrossRef" href="#bib0660"><span class="elsevierStyleSup">57</span></a> However, the orchestrated haemostatic imbalance observed in our study is similar with clinical findings by others where the release of TF and dimer was relatively higher in COC users when compared with women who did not use COCs.<a class="elsevierStyleCrossRefs" href="#bib0675"><span class="elsevierStyleSup">60–62</span></a> The outcome of study suggests a dose-dependent relationship between COC and haemostatic changes in association with progestin type.<a class="elsevierStyleCrossRefs" href="#bib0690"><span class="elsevierStyleSup">63,64</span></a></p><p id="par0120" class="elsevierStylePara elsevierViewall">TF plays an important role in the initiation of the extrinsic coagulation process which is complemented by the intrinsic pathway that ensures thrombin generation and clot production.<a class="elsevierStyleCrossRef" href="#bib0700"><span class="elsevierStyleSup">65</span></a> D-dimer antigen originates as a product of the fibrinolytic system that regulates the removal of fibrin during clot formation.<a class="elsevierStyleCrossRef" href="#bib0705"><span class="elsevierStyleSup">66</span></a> In principle, the fibrinolytic system physiologically counteracts the hypercoagulable condition and maintains normal circulation during haemostasis.<a class="elsevierStyleCrossRef" href="#bib0710"><span class="elsevierStyleSup">67</span></a> However, haemostatic imbalance can cause excessive fibrin deposition inside the vascular channels and obstruct blood flow which may lead to MACEs such as arterial and venous thrombosis, ischemia, and myocardial infarction.<a class="elsevierStyleCrossRef" href="#bib0710"><span class="elsevierStyleSup">67</span></a></p><p id="par0125" class="elsevierStylePara elsevierViewall">In terms of endothelial changes, the result of our study showed a significant increase in plasma levels of NO in HFD-fed rats when compared to LFD-fed rats after 8 weeks of HFD feeding. Meanwhile the plasma levels of vWF were comparable between both diet groups. This corresponds with previous findings where NO level was reduced in HFD-fed rats.<a class="elsevierStyleCrossRefs" href="#bib0715"><span class="elsevierStyleSup">68–71</span></a> Although recent evidence showed the critical role of vWF in the thrombo-inflammatory complex during obesity<a class="elsevierStyleCrossRef" href="#bib0735"><span class="elsevierStyleSup">72</span></a> where they mediate platelet aggregation and adhesion and promote leukocyte extravasation and several inflammatory responses.<a class="elsevierStyleCrossRef" href="#bib0450"><span class="elsevierStyleSup">15</span></a> Nonetheless, our result contrasts other previous studies that reported elevated levels of vWF in HFD-fed experimental animals.<a class="elsevierStyleCrossRefs" href="#bib0450"><span class="elsevierStyleSup">15,55</span></a></p><p id="par0130" class="elsevierStylePara elsevierViewall">Furthermore, HFD-fed rats treated with high dose COC for 6 weeks demonstrated increased levels of VWF while NO levels were significantly reduced when compared with the LFD. However, no significant change was observed when compared with HFD only group. The observed endothelial changes orchestrated by COC treatment may have resulted from vasoactive effect of the progestin component which is known to antagonize the vasodilatory effect of estrogen in healthy subjects.<a class="elsevierStyleCrossRefs" href="#bib0735"><span class="elsevierStyleSup">72,73</span></a> Our result also corroborates previous findings that showed reduced NO bioavailability during COC administration in non-obese animals.<a class="elsevierStyleCrossRef" href="#bib0635"><span class="elsevierStyleSup">52</span></a></p><p id="par0135" class="elsevierStylePara elsevierViewall">Of note, the association between the use of COC and the risk of CVDs events varies and it also depends on diverse factors.<a class="elsevierStyleCrossRef" href="#bib0745"><span class="elsevierStyleSup">74</span></a> For instance, in a multi-ethnic study of atherosclerosis that assessed the association of OC use and incident of heart failure (HF) in 3594 women, no overall increase in the risk of HF with OC use was reported.<a class="elsevierStyleCrossRef" href="#bib0750"><span class="elsevierStyleSup">75</span></a> In fact, recent study by Dou et al. showed that OC use was associated with a 9% reduction in the risk of CVD events including HF, and the association was significantly modified by the duration of OC use.<a class="elsevierStyleCrossRef" href="#bib0755"><span class="elsevierStyleSup">76</span></a> It is noteworthy that these studies did not report on the details of OC in terms of the formulation, dosage, and duration of use among the participants. In our study, we focused on the second-generation OC, and the outcome of our findings depict the notion that the short-term use of second-generation OC does not predispose to higher risk of CVD events. However, depending on the formulation, duration of use and the dosage of OC, the risk of CVD events may present with certain clinical manifestations. The limitations of this study include lack of determining vWF activity which is mainly secreted into circulation by endothelia cells. While vWF alone don’t offer a complete functional mechanism, vWF:Ristocetin ratio is important in associating vWF levels with CVD risk.<a class="elsevierStyleCrossRef" href="#bib0760"><span class="elsevierStyleSup">77</span></a> Furthermore, TF activity and sources of NO were not determined. Thus, further studies are required to determine how the long-term COC treatment influences the activity of vWF and TF activity in certain conditions related to postmenopausal state.</p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0155">Conclusion</span><p id="par0140" class="elsevierStylePara elsevierViewall">HFD-feeding aggravates the risk of atherothrombosis by orchestrating the concomitant release of pro-coagulants and endothelial activation markers leading to haemostatic imbalance and endothelial dysfunction. Short-term treatment with COC shows no detrimental effects. However, additional studies are required to confirm these findings, especially long-term effects of this treatment on CVD-related markers in conditions of obesity.</p></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0160">Authors’ contributions</span><p id="par0150" class="elsevierStylePara elsevierViewall">OA and BBN conceptualized, designed the study, and drafted the manuscript. OA and BBN performed formal analysis, methodology and validation. OA performed Visualization. OA, BBN and PVD writing-review & editing. PVD and BBN-Supervision. All authors approved the final manuscript.</p></span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0165">Data availability statement</span><p id="par0155" class="elsevierStylePara elsevierViewall">Data generated or analyzed during this study are available from the corresponding author upon reasonable request.</p></span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0170">Funding</span><p id="par0160" class="elsevierStylePara elsevierViewall">This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.</p></span><span id="sec0110" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0175">Conflict of interest</span><p id="par0165" class="elsevierStylePara elsevierViewall">The authors declare no conflict of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:16 [ 0 => array:3 [ "identificador" => "xres2102729" "titulo" => "Abstract" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abst0005" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abst0010" "titulo" => "Methods" ] 2 => array:2 [ "identificador" => "abst0015" "titulo" => "Results" ] 3 => array:2 [ "identificador" => "abst0020" "titulo" => "Conclusion" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec1791990" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xpalclavsec1791988" "titulo" => "Abbreviations" ] 3 => array:3 [ "identificador" => "xres2102730" "titulo" => "Resumen" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abst0025" "titulo" => "Antecedentes" ] 1 => array:2 [ "identificador" => "abst0030" "titulo" => "Métodos" ] 2 => array:2 [ "identificador" => "abst0035" "titulo" => "Resultados" ] 3 => array:2 [ "identificador" => "abst0040" "titulo" => "Conclusión" ] ] ] 4 => array:2 [ "identificador" => "xpalclavsec1791989" "titulo" => "Palabras clave" ] 5 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 6 => array:3 [ "identificador" => "sec0010" "titulo" => "Materials and methods" "secciones" => array:6 [ 0 => array:2 [ "identificador" => "sec0015" "titulo" => "Animal handlings" ] 1 => array:2 [ "identificador" => "sec0020" "titulo" => "Study design" ] 2 => array:2 [ "identificador" => "sec0025" "titulo" => "Measurement of hemodynamic variables" ] 3 => array:2 [ "identificador" => "sec0030" "titulo" => "Hemostatic assessment" ] 4 => array:2 [ "identificador" => "sec0035" "titulo" => "Biochemical analysis" ] 5 => array:2 [ "identificador" => "sec0040" "titulo" => "Statistical analysis" ] ] ] 7 => array:3 [ "identificador" => "sec0045" "titulo" => "Results" "secciones" => array:7 [ 0 => array:2 [ "identificador" => "sec0050" "titulo" => "Metabolic status of rats fed a high fat diet (HFD) compared to low fat diet (LFD) for 8 weeks" ] 1 => array:2 [ "identificador" => "sec0055" "titulo" => "Hemodynamic profile of LFD and HFD-fed rats for 8 weeks" ] 2 => array:2 [ "identificador" => "sec0060" "titulo" => "Haemostatic profile and endothelial markers of LFD and HFD-fed rats for 8 weeks" ] 3 => array:2 [ "identificador" => "sec0065" "titulo" => "Associations between MAP and markers of coagulation cascade and endothelial activation in rats fed HFD for 8 weeks" ] 4 => array:2 [ "identificador" => "sec0070" "titulo" => "Metabolic status of COC treated HFD-fed rats" ] 5 => array:2 [ "identificador" => "sec0075" "titulo" => "Effect of COC on hemodynamic parameters and haemostatic profile in HFD-fed rats" ] 6 => array:2 [ "identificador" => "sec0080" "titulo" => "Effect COC on biomarkers of coagulation and endothelial activation haemostatic profile in HFD-fed rats" ] ] ] 8 => array:2 [ "identificador" => "sec0085" "titulo" => "Discussion" ] 9 => array:2 [ "identificador" => "sec0090" "titulo" => "Conclusion" ] 10 => array:2 [ "identificador" => "sec0095" "titulo" => "Authors’ contributions" ] 11 => array:2 [ "identificador" => "sec0100" "titulo" => "Data availability statement" ] 12 => array:2 [ "identificador" => "sec0105" "titulo" => "Funding" ] 13 => array:2 [ "identificador" => "sec0110" "titulo" => "Conflict of interest" ] 14 => array:2 [ "identificador" => "xack732436" "titulo" => "Acknowledgements" ] 15 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2023-08-14" "fechaAceptado" => "2023-10-09" "PalabrasClave" => array:2 [ "en" => array:2 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1791990" "palabras" => array:6 [ 0 => "Combined oral contraceptive" 1 => "Cardiovascular disease" 2 => "High fat diet" 3 => "Obesity" 4 => "Coagulation" 5 => "Endothelial dysfunction" ] ] 1 => array:4 [ "clase" => "abr" "titulo" => "Abbreviations" "identificador" => "xpalclavsec1791988" "palabras" => array:9 [ 0 => "CVDs" 1 => "COCs" 2 => "TF" 3 => "NO" 4 => "vWF" 5 => "SBP" 6 => "DBP" 7 => "HR" 8 => "MACEs" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec1791989" "palabras" => array:6 [ 0 => "Anticonceptivo oral combinado" 1 => "Enfermedad cardiovascular" 2 => "Dieta alta en grasas" 3 => "Obesidad" 4 => "Coagulación" 5 => "Disfunción endotelial" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:3 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Background</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Combined oral contraceptives (COCs), use in individuals are associated with increased risk of thrombotic events. This highlights the significance of assessing the impact of COC on promoting coagulation and endothelial activation in high-fat diet (HFD)-fed Sprague Dawley rats.</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Methods</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Twenty (20) five-weeks-old female Sprague Dawley rats weighing between 150 and 200<span class="elsevierStyleHsp" style=""></span>g were subjected to both LFD and HFD-feeding for 8-weeks to determine its influence on basic metabolic status, hemostatic profile, hemodynamic parameters (blood pressure and heart rate), as well as selected biomarkers of coagulation (tissue factor and D-dimer) and endothelial activation (Von Willebrand factor and nitric oxide). Thereafter HFD-fed animals were treated with receive high dose combined oral contraceptive (HCOC) and low dose combine oral contraceptive (LCOC) for 6 weeks.</p></span> <span id="abst0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Results</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Our results showed that beyond weight gain, HFD-feeding was associated with hyperglycemia, increased mean arterial pressure, and reduced nitric oxide levels when compared with LFD group (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05). Interestingly, treatment with high dose of COC for 6-weeks did not significantly alter atherothrombotic markers (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0.05). However, this study is not without limitation as regulation of these markers remains to be confirmed within the cardiac tissues or endothelial cells of these animals.</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Conclusion</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">HFD-feeding orchestrate the concomitant release of pro-coagulants and endothelial activation markers in rats leading to haemostatic imbalance and endothelial dysfunction. Short-term treatment with COC shows no detrimental effects in these HFD-fed rats. Although in terms of clinical relevance, our findings depict the notion that the risk of CVD in association with COC may depend on the dosage and duration of use among other factors especially in certain conditions. However, additional studies are required to confirm these findings, especially long-term effects of this treatment within the cardiac tissues or endothelial cells of these animals in certain conditions relating to postmenopausal state.</p></span>" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abst0005" "titulo" => "Background" ] 1 => array:2 [ "identificador" => "abst0010" "titulo" => "Methods" ] 2 => array:2 [ "identificador" => "abst0015" "titulo" => "Results" ] 3 => array:2 [ "identificador" => "abst0020" "titulo" => "Conclusion" ] ] ] "es" => array:3 [ "titulo" => "Resumen" "resumen" => "<span id="abst0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Antecedentes</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">El uso de anticonceptivos orales combinados (AOC) en individuos se asocia con un mayor riesgo de eventos trombóticos. Esto resalta la importancia de evaluar el impacto de los AOC en la promoción de la coagulación y la activación endotelial en ratas Sprague Dawley alimentadas con una dieta alta en grasas (HFD).</p></span> <span id="abst0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Métodos</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Veinte (20) ratas Sprague Dawley hembra de 5<span class="elsevierStyleHsp" style=""></span>semanas de edad con un peso entre 150-200<span class="elsevierStyleHsp" style=""></span>g fueron tratadas mediante una alimentación con dieta baja en grasas (LFD) y alta en grasas (HFD) durante 8 semanas para determinar su influencia en el estado metabólico básico, perfil hemostático, parámetros hemodinámicos (presión arterial y frecuencia cardíaca), así como biomarcadores seleccionados de coagulación (factor tisular y D-dímero) y activación endotelial (factor de von Willebrand y óxido nítrico). Posteriormente, los animales alimentados con HFD fueron tratados con dosis alta de anticonceptivo oral combinado (AOC-AL) y dosis baja de anticonceptivo oral combinado (AOC-BL) durante 6 semanas.</p></span> <span id="abst0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Resultados</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Nuestros resultados mostraron que, además del aumento de peso, la alimentación con HFD se asoció con hiperglucemia, aumento de la presión arterial media y niveles reducidos de óxido nítrico en comparación con el grupo LFD (p<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0,05). Curiosamente, el tratamiento con dosis alta de AOC durante 6 semanas no alteró significativamente los marcadores aterotrombóticos (p<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>0,05). Sin embargo, este estudio no está exento de limitaciones, ya que la regulación de estos marcadores aún debe confirmarse en los tejidos cardíacos o las células endoteliales de estos animales.</p></span> <span id="abst0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conclusión</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">La alimentación con HFD orquesta la liberación concomitante de procoagulantes y marcadores de activación endotelial en ratas, lo que conduce a un desequilibrio hemostático y disfunción endotelial. El tratamiento a corto plazo con AOC no muestra efectos perjudiciales en estas ratas alimentadas con HFD. Aunque, en términos de relevancia clínica, nuestros hallazgos representan la idea de que el riesgo de enfermedad cardiovascular en relación con el AOC puede depender de la dosis y la duración de uso, entre otros factores, especialmente en ciertas condiciones. Sin embargo, se requieren estudios adicionales para confirmar estos hallazgos, especialmente los efectos a largo plazo de este tratamiento en los tejidos cardíacos o las células endoteliales de estos animales en ciertas condiciones relacionadas con el estado posmenopáusico.</p></span>" "secciones" => array:4 [ 0 => array:2 [ "identificador" => "abst0025" "titulo" => "Antecedentes" ] 1 => array:2 [ "identificador" => "abst0030" "titulo" => "Métodos" ] 2 => array:2 [ "identificador" => "abst0035" "titulo" => "Resultados" ] 3 => array:2 [ "identificador" => "abst0040" "titulo" => "Conclusión" ] ] ] ] "multimedia" => array:7 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1310 "Ancho" => 2925 "Tamanyo" => 292891 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Experimental design. 20 five-week-old female Sprague Dawley rats were used in this study. In experiment A rats were randomly allocated into two diet groups low-fat diet (LFD) and high-fat diet (HFD), (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>5) for a period of eight weeks. In experiment B, animals kept on HFD (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>10) were randomized to receive high dose combined oral contraceptive (HCOC) and low dose combine oral contraceptive (LCOC) for six weeks, to give total experimental period to be 14 weeks. The animal weights and metabolic changes were monitored weekly.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 670 "Ancho" => 1508 "Tamanyo" => 58385 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Effects of low-fat diet (LFD) and high fat diet (HFD) feeding on endothelial activation including (A) Von Willebrand factor (B) nitric oxide levels. All results are presented as mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>SEM with the significance represented by *<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05. Key: LFD: low-fat diet; HFD: high-fat diet; ns: (not significant).</p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 2261 "Ancho" => 3050 "Tamanyo" => 283669 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Association between Mean arterial pressure (MAP) and biomarkers of coagulation cascade like tissue factor (TF) and D-dimer (A, B) as well as biomarkers of endothelia activation such as Von Willebrand factor (VWF) and nitric oxide (NO) (C, D) after 8 weeks high fat diet (HFD)-feeding in rats. Correlations are presented as Pearson <span class="elsevierStyleItalic">r</span> 95% confidence interval (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05).</p>" ] ] 3 => array:7 [ "identificador" => "fig0020" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 769 "Ancho" => 1508 "Tamanyo" => 85296 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Effect of combined oral contraceptive treatment on biomarkers of coagulation cascade like tissue factor (A) and D-dimer (B). All results are presented as mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>SEM. Significance indicated between LFD and HFD<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>high dose COC. *<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05; **<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001. Key: LFD: low fat diet; HFD: high fat diet; COC: combined oral contraceptive.</p>" ] ] 4 => array:7 [ "identificador" => "fig0025" "etiqueta" => "Figure 5" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr5.jpeg" "Alto" => 711 "Ancho" => 1424 "Tamanyo" => 85638 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Effect of combined oral contraceptive treatment on biomarkers of endothelia activation like Von Willebrand factor (A) and nitric oxide (B). All results are presented as mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>SEM. Significance indicated between LFD and HFD<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>high dose COC. *<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05; **<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.001. Key: LFD: low fat diet; HFD: high fat diet; COC: combined oral contraceptive.</p>" ] ] 5 => array:8 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at1" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:2 [ "leyenda" => "<p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Results expressed as mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>standard error. Significance between groups (<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05) shown in boldface. Key: SBP: systolic blood pressure; DBP: diastolic blood pressure; MAP: mean arterial pressure; HR: heart rate; TF: tissue factor.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Parameters \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">LFD group \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">HFD group \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">p</span>-Value \t\t\t\t\t\t\n \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="4" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Metabolic status</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Food intake (g/kg/day) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">51.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">37.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold"><<span class="elsevierStyleHsp" style=""></span>0.0001</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Water intake (mL/kg/day) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">88.1<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.8 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">119<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.6 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold"><<span class="elsevierStyleHsp" style=""></span>0.0001</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Body weight (g) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">270<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>5.2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">289<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">0.02</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Fasting glycemia (mmol/L) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">3.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.6 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.5 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">0.006</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="4" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="4" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Hemodynamics</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>SBP (mmHg) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">129<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>5.7 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">137<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>7.2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.082 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>DBP (mmHg) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">90.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">92.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.9 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.166 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>MAP (mmHg) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">103.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>1.1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">107.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.9 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">0.03</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>HR (bpm) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">333<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>14.2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">380<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>20.7 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.174 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="4" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="4" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Hemostatic profile</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Bleeding time (s) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">204<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>39.1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">156<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>32.9 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.069 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>TF (pg/mL) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">53.84<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>6.7 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">76.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>9.9 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.09 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>D-dimer (ng/mL) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">175<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>17.1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">200<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>23 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.403 \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab3478996.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Characteristic features of rats exposed to high fat diet (HFD)-feeding in comparison to the low-fat diet (LFD) group.</p>" ] ] 6 => array:8 [ "identificador" => "tbl0010" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at2" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:2 [ "leyenda" => "<p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">Data presented as mean<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>SEM. SBP: systolic blood pressure; DBP: diastolic blood pressure; MAP: mean arterial pressure; HR: heart rate.</p><p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">Significance (<span class="elsevierStyleSup"><span class="elsevierStyleBold">a</span></span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05 vs LFD; <span class="elsevierStyleSup"><span class="elsevierStyleBold">b</span></span><span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>0.05 vs HFD) shown in boldface.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Parameters \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">LFD \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Untreated HFD \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">HFD<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>low dose COC \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black">HFD<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>high dose COC \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">p</span>-Value \t\t\t\t\t\t\n \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="6" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Metabolic status</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Food intake (g/kg/day) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">67.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">61.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.6 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">62.1<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">60<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>5.9<span class="elsevierStyleSup"><span class="elsevierStyleBold">a</span></span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">0.0347</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Water intake (mL/kg/day) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">102.5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.6 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">107.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>6.5 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">110<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">116.5<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>12.6 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.08 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Body weight (g) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">287.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>9.9 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">299.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>17 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">281.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>26.2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">295.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>11.3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.388 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Fasting glycemia (mmol/L) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">3.52<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.52 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.37 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">3.58<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.49 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">3.94<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.59 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.3424 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="6" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="6" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Hemodynamics</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>SBP (mmHg) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">125.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>5.4 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">135.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>8 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">137.0<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>7 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">140.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>7.4<span class="elsevierStyleSup"><span class="elsevierStyleBold">a</span></span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">0.0196</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>DBP (mmHg) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">88.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.7 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">91.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.8 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">91.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>0.84 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">92.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>6.15 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.5827 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>MAP (mmHg) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">100.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>4.3 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">106.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>3.1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">106.8<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>2.6 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">108.4<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>5.23<span class="elsevierStyleSup"><span class="elsevierStyleBold">a</span></span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">0.025</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>HR (bpm) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">343.2<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>39.5 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">361.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>27.1 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">357<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>17 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">385.6<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>27.8 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">0.1775 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="6" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span></td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " colspan="6" align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Hemostatic profile</span></td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Bleeding time (s) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">186<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>33 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">168<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>50.2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">120<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>37 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t">96<span class="elsevierStyleHsp" style=""></span>±<span class="elsevierStyleHsp" style=""></span>25.1<span class="elsevierStyleSup"><span class="elsevierStyleBold">ab</span></span> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="char" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">0.005</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab3478997.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">Characteristics of animals following 6-week short-term treatment with combined oral contraceptive (COC) (<span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>5/group).</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:77 [ 0 => array:3 [ "identificador" => "bib0380" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:1 [ "referenciaCompleta" => "WHO. 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