4.6 Article

The protective effect of resveratrol on vascular aging by modulation of the renine-angiotensin system

Journal

ATHEROSCLEROSIS
Volume 270, Issue -, Pages 123-131

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.atherosclerosis.2018.01.043

Keywords

Aorta; Arterial aging; Inflammation; Oxidative stress; Renine-angiotensin system; Resveratrol

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Science, ICT and future Planning [2014R1A1A3A04050919]
  2. Basic Science Research Program through the NRF
  3. Ministry of Education, Science and Technology [NRF-2016R1D1A1A09919985]

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Background and aims: This study evaluated the effects of resveratrol on arterial aging and the renin-angiotensin system (RAS) in mice and vascular smooth muscle cells (VSMCs). Methods: Aging mice were divided into control and resveratrol groups. Histological changes, inflammation, oxidative stress, RAS components, and the expression of AMP-activated protein kinase (AMPK), silent information regulator T1 (SIRT1), peroxisome proliferator-activated receptor-gamma co-activator 1 alpha (PGC-1 alpha), and anti-oxidative enzymes was measured in thoracic aortas of 24-month-old mice. The effect of resveratrol on fibrosis, cell senescence, and RAS components was also investigated in VSMCs stimulated by angiotensin (Ang) II. Results: Aorta media thickness, inflammation, fibrosis, and oxidative stress were significantly lower in the resveratrol group than in the control group. Resveratrol treatment decreased serum Ang II level and the aortic expression of prorenin receptor (PRR) and angiotensin converting enzyme (ACE), and increased serum Ang-(1-7) level and the expression of ACE2, Ang II type 2 receptor (AT2R), and Mas receptor (MasR). Resveratrol increased the expression of phosphorylated AMPK, SIRT1, PGC-1 alpha, phosphorylated endothelial nitric oxide synthase and superoxide dismutase 1 and 2, and decreased that of NADPH oxidase 2 and 4. In Ang II-stimulated VSMCs, resveratrol treatment markedly decreased the number of senescence associated beta-galactosidase stained cells and pro-fibrotic protein expression and increased the expression of AT2R and MasR. Conclusions: Resveratrol protects against arterial aging and this effect is associated with reduced activity of the PRReACEeAng II axis and stimulation of the ACE2-Ang-(1-7)-ATR2-MasR axis. (C) 2018 Elsevier B.V. All rights reserved.

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