Peroxynitrite-Mediated SIRT (Sirtuin)-1 Inactivation Contributes to Nicotine-Induced Arterial Stiffness in Mice. Issue 7 (July 2019)

• Record Type: Journal Article
• Authors: Ding, Ye; Han, Yi; Lu, Qiulun; An, Junqing; Zhu, Huaiping; Xie, Zhonglin; Song, Ping; Zou, Ming-Hui
• Is Part Of: Arteriosclerosis, thrombosis, and vascular biology. Volume 39:Issue 7(2019)
• Publication Date: 2019-07
• Subjects: collagen -- cysteine -- extracellular matrix -- nicotine -- serine; Arteriosclerosis -- Periodicals; Thrombosis -- Periodicals; Blood-vessels -- Pathophysiology -- Periodicals; Electronic journals; 616.13
• DOI: 10.1161/ATVBAHA.118.312346
• Languages: English
• ISSNs: 1079-5642

Abstract

Abstract : Objective—: Inhibition of SIRT (sirtuin)-1, a nicotinamide adenine dinucleotide-dependent protein deacetylase, is linked to cigarette smoking-induced arterial stiffness, but the underlying mechanisms remain largely unknown. The aim of the present study was to determine the effects and mechanisms of nicotine, a major component of cigarette smoke, on SIRT1 activity and arterial stiffness. Approach and Results—: Arterial stiffness, peroxynitrite (ONOO − ) formation, SIRT1 expression and activity were monitored in mouse aortas of 8-week-old C57BL/6 mice (wild-type) or Sirt1 -overexpressing ( Sirt1 Super ) mice with or without nicotine for 4 weeks. In aortas of wild-type mice, nicotine reduced SIRT1 protein and activity by ≈50% without affecting its mRNA levels. In those from Sirt1 Super mice, nicotine also markedly reduced SIRT1 protein and activity to the levels that were comparable to those in wild-type mice. Nicotine infusion significantly induced collagen I, fibronectin, and arterial stiffness in wild-type but not Sirt1 Super mice. Nicotine increased the levels of iNOS (inducible nitric oxide synthase) and the co-staining of SIRT1 and 3-nitrotyrosine, a footprint of ONOO − in aortas. Tempol, which ablated ONOO − by scavenging superoxide anion, reduced the effects of nicotine on SIRT1 and collagen. Mutation of zinc-binding cysteine 395 or 398 in SIRT1 into serine (C395S) or (C398S) abolished SIRT1 activity. Furthermore, ONOO − dose-dependently inhibited the enzyme and increased zinc release in recombinant SIRT1. Finally, we found SIRT1 inactivation by ONOO − activated the YAP (Yes-associated protein) resulting in abnormal ECM (extracellular matrix) remodeling. Conclusions—: Nicotine induces ONOO −, which selectively inhibits SIRT1 resulting in a YAP-mediated ECM remodeling. Abstract : Supplemental Digital Content is available in the text.