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J Atheroscler Thromb. 2014;21(10):997-1010.

Antioxidant effects of statins in the management of cardiometabolic disorders.

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제1저자 임수 · 교신저자 임수

PMID 25132378 DOI 10.5551/jat.24398 IF 3.4 내분비대사내과
소속 (1)
  1. Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine.

Abstract

Redox systems are key players in vascular health. A shift in redox homeostasis-that results in an imbalance between reactive oxygen species (ROS) generation and endogenous antioxidant defenses has the potential to create a state of oxidative stress that subsequently plays a role in the pathogenesis of a number of diseases, including those of the cardiovascular and metabolic system. Statins, which are primarily used to reduce the concentration of low-density lipoprotein cholesterol, have also been shown to reduce oxidative stress by modulating redox systems. Studies conducted both in vitro and in vivo support the role of oxidative stress in the development of atherosclerosis and cardiovascular diseases. Oxidative stress may also be responsible for various diabetic complications and the development of fatty liver. Statins reduce oxidative stress by blocking the generation of ROS and reducing the NAD+/NADH ratio. These drugs also have effects on nitric oxide synthase, lipid peroxidation and the adiponectin levels. It is possible that the antioxidant properties of statins contribute to their protective cardiovascular effects, independent of the lipid-lowering actions of these agents. However, possible adverse effects of statins on glucose homeostasis may be related to the redox system. Therefore, studies investigating the modulation of redox signaling by statins are warranted.

그 밖의 정보
출판 형태
Journal Article, Research Support, Non-U.S. Gov't, Review
저널
Journal of atherosclerosis and thrombosis · eISSN 1880-3873
전자 출판
2014-08-15
MeSH
Antioxidants / therapeutic use · Disease Progression · Heart Diseases / drug therapy · Humans · Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use · Insulin Resistance · Metabolic Diseases / drug therapy · Oxidation-Reduction
Substances
Antioxidants · Hydroxymethylglutaryl-CoA Reductase Inhibitors