{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,4]],"date-time":"2026-06-04T16:32:34Z","timestamp":1780590754134,"version":"3.54.1"},"reference-count":78,"publisher":"American Physiological Society","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American Journal of Physiology-Heart and Circulatory Physiology"],"published-print":{"date-parts":[[2018,12,1]]},"abstract":"<jats:p> Overconsumption of a diet rich in fat and carbohydrates, called the Western diet, is a major contributor to the global epidemic of cardiovascular disease. Despite previously documented cardiovascular protection exhibited in female rats, this safeguard may be lost under certain metabolic stressors. We hypothesized that female Wistar rats challenged by a Western diet composed of 21% fat and 50% carbohydrate (34.1% sucrose) for 17 wk would develop endothelial dysfunction via endothelial Toll-like receptor 4 (TLR4) signaling. Western diet-fed female rats exhibited dysregulation of metabolism, revealing increased body weight and abdominal fat, decreased expression of adiponectin in white adipose tissue, glucose intolerance, and impaired insulin sensitivity. Western diet exposure increased hepatic triglycerides and cholesterol alongside hepatic steatosis, categorizing nonalcoholic fatty liver disease. Moreover, a Western diet negatively affected vascular function, revealing hypertension, impaired endothelium-dependent vasorelaxation, aortic remodeling, and increased reactive oxygen species (ROS) production. Aortic protein expression of TLR4 and its downstream proteins were markedly increased in the Western diet-fed group in association with elevated serum levels of free fatty acids. In vitro experiments were conducted to test whether free fatty acids contribute to vascular ROS overproduction via the TLR4 signaling pathway. Cultured endothelial cells were stimulated with palmitate in the presence of TAK-242, a TLR4 signaling inhibitor. Palmitate-induced overgeneration of ROS in endothelial cells was abolished in the presence of TAK-242. Our data show that a Western diet induced endothelial dysfunction in female rats and suggest that endothelial TLR4 signaling may play a key role in abolishing female cardiovascular protection. <\/jats:p><jats:p> NEW &amp; NOTEWORTHY A Western diet induced elevated levels of free fatty acids, produced nonalcoholic fatty liver disease, and provoked endothelial dysfunction in female rats in association with Toll-like receptor 4 signaling-mediated vascular reactive oxygen species production. Limited consumption of a Western diet in premenopausal women may decrease their risk of cardiovascular complications. <\/jats:p>","DOI":"10.1152\/ajpheart.00218.2018","type":"journal-article","created":{"date-parts":[[2018,9,28]],"date-time":"2018-09-28T14:31:28Z","timestamp":1538145088000},"page":"H1735-H1747","source":"Crossref","is-referenced-by-count":36,"title":["Western diet triggers Toll-like receptor 4 signaling-induced endothelial dysfunction in female Wistar rats"],"prefix":"10.1152","volume":"315","author":[{"given":"Benjamin","family":"Kramer","sequence":"first","affiliation":[{"name":"Department of Biomedical Sciences, College of Osteopathic Medicine, New York Institute of Technology, Old Westbury, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lucas Martins","family":"Fran\u00e7a","sequence":"additional","affiliation":[{"name":"Laboratory of Experimental Physiology, Department of Physiological Sciences, Federal University of Maranh\u00e3o, Sao Luis, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Youhua","family":"Zhang","sequence":"additional","affiliation":[{"name":"Department of Biomedical Sciences, College of Osteopathic Medicine, New York Institute of Technology, Old Westbury, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Antonio Marcus de Andrade","family":"Paes","sequence":"additional","affiliation":[{"name":"Laboratory of Experimental Physiology, Department of Physiological Sciences, Federal University of Maranh\u00e3o, Sao Luis, Brazil"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A. 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