High fat diet-induced metabolically obese and normal weight rabbit model shows early vascular dysfunction: mechanisms involved

• Published in: International Journal of Obesity 2018-09, Vol.42 (9), p.1535-1543
• Main Authors: Alarcon, Gabriela, Roco, Julieta, Medina, Mirta, Medina, Analia, Peral, Maria, Jerez, Susana
• Format: Article
• Language: English
• Subjects: 13; 13/51; 64; 692/163/2743/2037; 692/499; 692/699/75; 82; 82/80; 9/10; Acetylcholine; Adipose tissue; Analysis; Angiotensin; Angiotensin II; Angiotensins; Aorta; Arteries; Biological markers; Biomarkers; Blood vessels; Body weight; C-reactive protein; Cardiovascular diseases; Cardiovascular tests; Cholesterol; Contractility; Controlled conditions; COX-2 inhibitors; Cyclooxygenase-1; Cyclooxygenase-2; Diet; Endothelium; Epidemiology; Fasting; Glucose; Glucose intolerance; Glucose tolerance; Health Promotion and Disease Prevention; High fat diet; Immunohistochemistry; Inflammation; Influence; Internal Medicine; Intolerance; Medicine; Medicine & Public Health; Metabolic Diseases; Metabolic disorders; Metabolic syndrome; Metabolism; Nitrites; Norepinephrine; Obesity; Oxidative stress; Proteins; Public Health; Rabbits; Thorax; Triglycerides; Vasodilation
• ISSN: 0307-0565; 1476-5497
• DOI: 10.1038/s41366-018-0020-6

Background Obesity contributes significantly to the development and evolution of cardiovascular disease (CVD) which is believed to be mediated by oxidative stress, inflammation and endothelial dysfunction. However, the vascular health of metabolically obese and normal weight (MONW) individuals is not completely comprehended. Objectives The purpose of our study was to evaluate vascular function on the basis of a high fat diet (HFD)-MONW rabbit model. Subjects Twenty four male rabbits were randomly assigned to receive either a regular diet (CD, n  = 12) or a high-fat diet (18% extra fat on the regular diet, HFD, n  = 12) for 6 weeks. Results Body weight, TBARS and gluthathione serum levels were similar between the groups; fasting glucose, triglycerides, C reactive protein (CRP), visceral adipose tissue (VAT), triglyceride-glucose index (TyG index) were higher in the HFD group. Compared to CD, the HFD rabbits had glucose intolerance and lower HDL-cholesterol and plasma nitrites levels. Thoracic aortic rings from HFD rabbits exhibited: (a) a reduced acetylcholine-induced vasorelaxation; (b) a greater contractile response to norepinephrine and KCl; (c) an improved angiotensin II-sensibility. The HFD-effect on acetylcholine-response was reversed by the cyclooxygenase-2 (COX-2) inhibitor (NS398) and the cyclooxygenase-1 inhibitor (SC560), and the HFD-effect on angiotensin II was reversed by NS398 and the TP receptor blocker (SQ29538). Immunohistochemistry and western blot studies showed COX-2 expression only in arteries from HFD rabbits. Conclusions Our study shows a positive pro-inflammatory status of HFD-induced MONW characterized by raised COX-2 expression, increase of the CRP levels, reduction of NO release and oxidative stress-controlled conditions in an early stage of metabolic alterations characteristic of metabolic syndrome. Endothelial dysfunction and increased vascular reactivity in MONW individuals may be biomarkers of early vascular injury. Therefore, the metabolic changes induced by HFD even in normal weight individuals may be associated to functional alterations of blood vessels.