Glutathione-S-transferase P protects against endothelial dysfunction induced by exposure to tobacco smoke

被引:87
作者
Conklin, Daniel J. [1 ]
Haberzettl, Petra
Prough, Russell A. [2 ]
Bhatnagar, Aruni [2 ]
机构
[1] Univ Louisville, Dept Med, Div Cardiovasc Med, Inst Mol Cardiol, Louisville, KY 40202 USA
[2] Univ Louisville, Dept Biochem & Mol Biol, Louisville, KY 40202 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2009年 / 296卷 / 05期
基金
美国国家卫生研究院;
关键词
acrolein; aldehydes; environmental cardiology; oxidative stress; CIGARETTE MAINSTREAM SMOKE; NITRIC-OXIDE BIOSYNTHESIS; HEALTHY-YOUNG ADULTS; MYOCARDIAL-INFARCTION; MASS-SPECTROMETRY; ALLELIC VARIANTS; SECONDHAND SMOKE; DNA-DAMAGE; CANCER; RISK;
D O I
10.1152/ajpheart.00867.2008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Conklin DJ, Haberzettl P, Prough RA, Bhatnagar A. Glutathione-S-transferase P protects against endothelial dysfunction induced by exposure to tobacco smoke. Am J Physiol Heart Circ Physiol 296: H1586-H1597, 2009. First published March 6, 2009; doi:10.1152/ajpheart.00867.2008.-Exposure to tobacco smoke impairs endothelium-dependent arterial dilation. Reactive constituents of cigarette smoke are metabolized and detoxified by glutathione-S-transferases (GSTs). Although polymorphisms in GST genes are associated with the risk of cancer in smokers, the role of these enzymes in regulating the cardiovascular effects of smoking has not been studied. The P isoform of GST (GSTP), which catalyzes the conjugation of electrophilic molecules in cigarette smoke such as acrolein, was expressed in high abundance in the mouse lung and aorta. Exposure to tobacco smoke for 3 days (5 h/day) decreased total plasma protein. These changes were exaggerated in GSTP(-/-) mice. Aortic rings isolated from tobacco smoke-exposed GSTP(-/-) mice showed greater attenuation of ACh-evoked relaxation than those from GSTP(-/-) mice. The lung, plasma, and aorta of mice exposed to tobacco smoke or acrolein (for 5 h) accumulated more acrolein-adducted proteins than those tissues of mice exposed to air, indicating that exposure to tobacco smoke results in the systemic delivery of acrolein. Relative to GSTP(-/-) mice, modification of some proteins by acrolein was increased in the aorta of GSTP(-/-) mice. Aortic rings prepared from GSTP(-/-) mice that inhaled acrolein (1 ppm, 5 h/day for 3 days) or those exposed to acrolein in an organ bath showed diminished ACh-induced arterial relaxation more strongly than GSTP(-/-) mice. Acrolein-induced endothelial dysfunction was prevented by pretreatment of the aorta with N-acetylcysteine. These results indicate that GSTP protects against the endothelial dysfunction induced by tobacco smoke exposure and that this protection may be related to the detoxification of acrolein or other related cigarette smoke constituents.
引用
收藏
页码:H1586 / H1597
页数:12
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