Regulation of vascular smooth muscle cell growth by aldose reductase

被引:9
作者
Bhatnagar, A
Ruef, J
Liu, SQ
Srivastava, S
Srivastava, SK
机构
[1] Univ Louisville, Jewish Cardiovasc Res Ctr, Div Cardiol, Dept Med, Louisville, KY 40202 USA
[2] Univ Heidelberg, Div Cardiol, Heidelberg, Germany
[3] Univ Texas, Med Branch, Galveston, TX 77555 USA
关键词
aldose reductase; rat carotid artery; restenosis; vascular smooth muscle cells;
D O I
10.1016/S0009-2797(00)00290-8
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
Aldose reductase (AR) is a broad-specificity aldo-keto reductase with wide species and tissue distribution. The enzyme has been implicated in the development of pleiotropic complications of long-term diabetes. However, the euglycemic function of the enzyme remains unclear. To examine its potential role in cell growth, changes in AR mRNA and protein were measured in human aortic smooth muscle cells exposed in culture to serum or thrombin. Stimulation by these mitogens led to an increase in the abundance of AR mRNA and protein. Furthermore, inhibition of the AR by tolrestat and sorbinil diminished DNA synthesis and cell proliferation in response to serum. Immunohistochemical staining with anti-AR antibodies revealed no significant expression of AR in the smooth muscle cells of rat carotid arteries. However, 10 and 21 days after balloon injury, intense staining was associated with the proliferating cells of the neointima. Treatment of these animals with 40 mg/kg/day sorbinil diminished the ratio of neointima to the media. Together, these observations suggest that, in vascular smooth muscle cells (VSMC), AR is a growth-responsive gene product and that inhibition of AR prevents VSMC growth and decreases intimal hyperplasia and restenosis. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:627 / 636
页数:10
相关论文
共 17 条
[1]   ALDOSE REDUCTASE - CONGENIAL AND INJURIOUS PROFILES OF AN ENIGMATIC ENZYME [J].
BHATNAGAR, A ;
SRIVASTAVA, SK .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1992, 48 (02) :91-121
[2]   Contribution of ATP to oxidative stress-induced changes in action potential of isolated cardiac myocytes [J].
Bhatnagar, A .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 272 (04) :H1598-H1608
[3]   CHEMISTRY AND BIOCHEMISTRY OF 4-HYDROXYNONENAL, MALONALDEHYDE AND RELATED ALDEHYDES [J].
ESTERBAUER, H ;
SCHAUR, RJ ;
ZOLLNER, H .
FREE RADICAL BIOLOGY AND MEDICINE, 1991, 11 (01) :81-128
[4]   Molecular therapies for vascular diseases [J].
Gibbons, GH ;
Dzau, VJ .
SCIENCE, 1996, 272 (5262) :689-693
[5]  
Gittenberger-de Groot AC, 1999, ARTERIOSCL THROM VAS, V19, P1589
[6]   An essential role for free radicals and derived species in signal transduction [J].
Lander, HM .
FASEB JOURNAL, 1997, 11 (02) :118-124
[7]   IMMUNOHISTOCHEMICAL LOCALIZATION OF ALDOSE REDUCTASE .1. ENZYME-PURIFICATION AND ANTIBODY PREPARATION - LOCALIZATION IN PERIPHERAL-NERVE, ARTERY, AND TESTIS [J].
LUDVIGSON, MA ;
SORENSON, RL .
DIABETES, 1980, 29 (06) :438-449
[8]   Aldose reductase functions as a detoxification system for lipid peroxidation products in vasculitis [J].
Rittner, HL ;
Hafner, V ;
Klimiuk, PA ;
Szweda, LI ;
Goronzy, JJ ;
Weyand, CM .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (07) :1007-1013
[9]   THE PATHOGENESIS OF ATHEROSCLEROSIS - A PERSPECTIVE FOR THE 1990S [J].
ROSS, R .
NATURE, 1993, 362 (6423) :801-809
[10]   Induction of rat aortic smooth muscle cell growth by the lipid peroxidation product 4-hydroxy-2-nonenal [J].
Ruef, J ;
Rao, GN ;
Li, FZ ;
Bode, C ;
Patterson, C ;
Bhatnagar, A ;
Runge, MS .
CIRCULATION, 1998, 97 (11) :1071-1078