Nicotinic acid inhibits vascular inflammation via the SIRT1-dependent signaling pathway

卷:26

Li, Yanxiang ; Yang, Guangde ; Yang, Xiaofeng ; He, Yanhao ; Wang, Weirong ; Zhang, Jiye ; Li, Tingting ; Zhang, Wei ; Lin, Rong

关键词: Nicotinic acid;    SIRT1;    Inflammation;    Cluster of differentiation 40;    Endothelium;   

DOI  :  10.1016/j.jnutbio.2015.07.006

学科分类：食品科学和技术

【 摘 要 】

Nicotinic acid (NA) has recently been shown to inhibit inflammatory response in cardiovascular disease. Sirtuin1 (SIRT1), a NAD(+)-dependent class III histone deacetylase, participates in the regulation of cellular inflammation. We hypothesized that dietary supplementation of NA could attenuate vascular inflammation via modulation of SIRT1 pathway. New Zealand White rabbits received chow or chow supplemented with 0.6% (wt/wt) NA for 2 weeks. Acute vascular inflammation was induced in the animals by placing a non-occlusive silastic collar around the left common carotid artery. At 24 h after collar implantation, the collar-induced production of C-reactive protein and monocyte chemotactic protein-1 was significantly suppressed in the NA-supplemented animals. Meanwhile, NA also decreased the expression of cluster of differentiation 40 (CD40) and CD40 ligand, but up-regulated SIRT1 expression, both in rabbits and in lipopolysaccharide-stimulated endothelial cells. Moreover, knockdown of SIRT1 reversed the inhibitory effect of NA on CD40 expression. Further study revealed that NA also decreased the expression of CD40 partly through mammalian target of rapamycin. These results indicate that NA protects against vascular inflammation via the SIRT1/CD40-dependent signaling pathway. (C) 2015 Elsevier Inc. All rights reserved.