Abstract

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.

Highlights

  • The reduced sirtuin 1 (SIRT1) activity was associated with an enhanced acetylation of the endothelial nitric oxide synthase in the perivascular adipose tissue (PVAT)

  • We show that high-fat diet (HFD)-induced vascular dysfunction is only evident in PVAT-containing but not in PVAT-free aorta

  • We reported that PVAT dysfunction in obesity was associated with an enhanced endothelial nitric oxide synthase (eNOS) acetylation and reduced the eNOS activity [11]

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Summary

Introduction

Over the past few decades, the prevalence of obesity has become a major health challenge around the world [1]. For many cancer types, but obesity is a risk factor for cardiovascular disease and metabolic syndrome [2]. Obesity has numerous adverse effects on hemodynamics and cardiovascular structure and function [3]. In obese patients or patients with metabolic syndrome, vascular dysfunction is evident in both large conduits [4] and small arteries [5]. Patients with obesity have a higher risk of developing hypertension and stroke [3]. In addition to its structural supporting role for the blood vessels, perivascular adipose tissue (PVAT) is involved in regulating vascular biology [6]. The nitric oxide (NO)producing enzyme endothelial NO synthase (eNOS) is expressed in the PVAT, and PVAT eNOS plays an important role in regulating vascular function [7–9]

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