Xia Ning, Reifenberg Gisela, Schirra Christian, Li Huige
Department of Pharmacology, Johannes Gutenberg University Medical Center, Langenbeckstr. 1, 55131 Mainz, Germany.
Antioxidants (Basel). 2022 Mar 12;11(3):541. doi: 10.3390/antiox11030541.
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.
高脂饮食(HFD)诱导的小鼠血管损伤与血管周围脂肪组织(PVAT)功能障碍有关。本研究旨在调查沉默调节蛋白1(SIRT1)的作用。雄性C57BL/6J小鼠喂食HFD 20周以诱导肥胖。使用线肌张力描记系统分析血管功能。在肥胖小鼠中,含PVAT的主动脉对乙酰胆碱的血管舒张反应降低,尽管不含PVAT的主动脉血管功能仍正常。尽管SIRT1表达增强,但肥胖小鼠PVAT中的SIRT1活性降低。肥胖小鼠PVAT中的烟酰胺腺嘌呤二核苷酸(NAD)水平和NAD/NADH比值降低,这可能归因于产生NAD的酶烟酰胺磷酸核糖转移酶(NAMPT)的下调。SIRT1活性降低与PVAT中内皮型一氧化氮合酶(eNOS)的乙酰化增强有关。用NAD对肥胖小鼠含PVAT的主动脉进行离体孵育可使血管功能完全恢复正常。因此,NAD缺乏导致的SIRT1活性降低与肥胖诱导的PVAT功能障碍有关。