Simvastatin and oxidative stress in humans: A randomized, double blinded, placebo-controlled clinical trial

被引:71
作者
Rasmussen, Sanne Tofte [1 ]
Andersen, Jon Traerup [2 ]
Nielsen, Torben Kjaer [1 ]
Cejvanovic, Vanja [1 ]
Petersen, Kasper Meidahl [1 ]
Henriksen, Trine [1 ]
Weimann, Allan [1 ]
Lykkesfeldt, Jens [3 ]
Poulsen, Henrik Enghusen [1 ,2 ,4 ]
机构
[1] Rigshosp, Lab Clin Pharmacol, Ole Maaloes Vej 26,Entrance 76,Sect Q7642, DK-2200 Copenhagen N, Denmark
[2] Bispebjerg Frederiksberg Hosp, Dept Clin Pharmacol, Bispebjerg Bakke 23, DK-2400 Copenhagen NW, Denmark
[3] Univ Copenhagen, Fac Hlth & Med Sci, Sect Expt Anim Models, Ridebanevej 9, DK-1870 Frederiksberg C, Denmark
[4] Univ Copenhagen, Inst Clin Med, Univ Copenhagen Hosp, Fac Hlth & Med Sci, DK-1168 Copenhagen, Denmark
关键词
Simvastatin; Randomized clinical trial; Oxidative stress; Reactive oxygen species; 8-oxodg; 8-oxoguo; DNA oxidation; RNA oxidation; STATINS; DISEASE; PLASMA; URINE; ACID; MALONDIALDEHYDE; MITOCHONDRIA; MECHANISM; ASCORBATE; HPLC;
D O I
10.1016/j.redox.2016.05.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Simvastatin reduces the blood concentration of cholesterol by inhibiting hydroxymethylglutaryl-coenzyme A reductase, the rate-limiting enzyme in cholesterol synthesis, and thereby reduces the risk of cardiovascular disease. In addition, simvastatin treatment leads to a reduction in fluxes in mitochondrial respiratory complexes I and II and might thereby reduce the formation of reactive oxygen species, which have been implicated in the pathogenesis of arteriosclerosis. Therefore, we hypothesized that simvastatin may reduce oxidative stress in humans in vivo. We conducted a randomized, double-blinded, placebo-controlled study in which subjects were treated with either 40 mg of simvastatin or placebo for 14 days. The endpoints were six biomarkers for oxidative stress, which represent intracellular oxidative stress to nucleic acids, lipid peroxidation and plasma antioxidants, that were measured in urine and plasma samples. A total of 40 participants were included, of which 39 completed the trial. The observed differences between simvastatin and placebo groups in the primary outcomes, DNA and RNA oxidation, were small and nonsignificant (p=0.68), specifically, 3% in the simvastatin group compared to 7.1% in the placebo group for DNA oxidation and 7.3% in the simvastatin group compared to 3.4% in the placebo group. The differences in biomarkers related to plasma were not statistically significant between the treatments groups, with the exception of total vitamin E levels, which, as expected, were reduced in parallel with the reduction in plasma cholesterol. In healthy young male volunteers, short-term simvastatin treatment, which considerably reduces cholesterol, does not lead to a clinically relevant reduction in a panel of measures of oxidative stress. Whether simvastatin has effects on oxidative stress in diseased populations, such as diabetes or hemochromatosis, where oxidative stress is prominent, is unknown but seems unlikely. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:32 / 38
页数:7
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