High-fat diet (HFD)-induced vascular impairment in mice is associated with a dysfunction of the perivascular adipose tissue (PVAT). The present study was conducted to investigate the involvement of sirtuin 1 (SIRT1). Male C57BL/6J mice were fed an HFD for 20 weeks to induce obesity. Vascular function was analyzed using a wire myograph system. In obese mice, the vasodilator response of PVAT-containing aortas to acetylcholine was reduced, although the vascular function of PVAT-free aortas remained normal. SIRT1 activity in PVAT of obese mice was reduced despite enhanced SIRT1 expression. Nicotinamide adenine dinucleotide (NAD + ) levels and the NAD + /NADH ratio in the PVAT of obese mice were decreased, which was likely attributable to a downregulation of the NAD + -producing enzyme NAMPT. The reduced SIRT1 activity was associated with an enhanced acetylation of the endothelial nitric oxide synthase (eNOS) in the PVAT. Ex vivo incubation of PVAT-containing aorta from obese mice with NAD + led to a complete normalization of vascular function. Thus, reduced SIRT1 activity due to NAD + deficiency is involved in obesity-induced PVAT dysfunction.
Keyphrases
- high fat diet induced
- insulin resistance
- high fat diet
- adipose tissue
- oxidative stress
- nitric oxide synthase
- diabetic rats
- metabolic syndrome
- skeletal muscle
- ischemia reperfusion injury
- type diabetes
- high glucose
- nitric oxide
- endothelial cells
- weight loss
- pulmonary artery
- cell proliferation
- aortic valve
- pulmonary arterial hypertension
- coronary artery
- signaling pathway
- weight gain