Aldose reductase in diabetic microvascular complications

被引:102
作者
Chung, SSM [1 ]
Chung, SK [1 ]
机构
[1] Univ Hong Kong, Inst Mol Biol, Hong Kong, Hong Kong, Peoples R China
关键词
aldose reductase; polyol pathway; diabetic complications; microvascular;
D O I
10.2174/1389450054021891
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Most long-term diabetic patients develop microvascular diseases such as retinopathy, nephropathy and neuropathy. Although tight control of blood glucose greatly reduces the incidence of these complications, a significant fraction of diabetic patients with good glycemic control still develop these diseases. Therefore, it is imperative to understand the underlying mechanisms of these diseases such that effective treatment or preventive methods can be developed to augment euglycemic control. In animal studies, there is strong evidence that aldose reductase, the first and rate-limiting enzyme of the polyol pathway that converts glucose to fructose, plays a key role in the pathogenesis of microvascular complications. However, clinical trials of the aldose reductase inhibitors were disappointing and several pharmaceutical companies had abandoned the development of this line of drugs. In this review, the potential pathogenic mechanisms of the polyol pathway are presented, the evidence for the involvement of the polyol pathway in diabetic complications summarized, and the reasons for the unimpressive results of the clinical trials of the aldose inhibitors discussed. It appears that renewed efforts to develop aldose reductase inhibitors for the treatment and prevention of diabetic complications are warranted.
引用
收藏
页码:475 / 486
页数:12
相关论文
共 157 条
[1]   LOCALIZATION OF ALDOSE REDUCTASE IN THE HUMAN-EYE [J].
AKAGI, Y ;
YAJIMA, Y ;
KADOR, PF ;
KUWABARA, T ;
KINOSHITA, JH .
DIABETES, 1984, 33 (06) :562-566
[2]   Minalrestat, an aldose reductase inhibitor, corrects the impaired microvascular reactivity in diabetes [J].
Akamine, EH ;
Hohman, TC ;
Nigro, D ;
Carvalho, MHC ;
Tostes, RD ;
Fortes, ZB .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (03) :1236-1242
[3]   Overview of studies on metabolic and vascular regulatory changes in early diabetic retinopathy [J].
Alder, VA ;
Su, EN ;
Yu, DY ;
Cringle, S ;
Yu, P .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF OPHTHALMOLOGY, 1998, 26 (02) :141-148
[4]   Use of genetic mouse models in the study of diabetic nephropathy [J].
Allen T.J. ;
Cooper M.E. ;
Lan H.Y. .
Current Atherosclerosis Reports, 2004, 6 (3) :197-202
[5]   Pericytes: Cell biology and pathology [J].
Allt, G ;
Lawrenson, JG .
CELLS TISSUES ORGANS, 2001, 169 (01) :1-11
[6]   Sorbitol dehydrogenase overexpression potentiates glucose toxicity to cultured retinal pericytes [J].
Amano, S ;
Yamagishi, S ;
Kato, N ;
Inagaki, Y ;
Okamoto, T ;
Makino, M ;
Taniko, K ;
Hirooka, H ;
Jomori, T ;
Takeuchi, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 299 (02) :183-188
[7]   Enzymatic function of nitric oxide synthases [J].
Andrew, PJ ;
Mayer, B .
CARDIOVASCULAR RESEARCH, 1999, 43 (03) :521-531
[8]   CHARACTERIZATION OF A NOVEL ALDOSE REDUCTASE INHIBITOR, FR74366, AND ITS EFFECTS ON DIABETIC CATARACT AND NEUROPATHY IN THE RAT [J].
AO, S ;
SHINGU, Y ;
KIKUCHI, C ;
TAKANO, Y ;
NOMURA, K ;
FUJIWARA, T ;
OHKUBO, Y ;
NOTSU, Y ;
YAMAGUCHI, I .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1991, 40 (01) :77-87
[9]   A role for the polyol pathway in the early neuroretinal apoptosis and glial changes induced by diabetes in the rat [J].
Asnaghi, V ;
Gerhardinger, C ;
Hoehn, T ;
Adeboje, A ;
Lorenzi, M .
DIABETES, 2003, 52 (02) :506-511
[10]   SORBINIL PREVENTS GLOMERULAR HYPERPERFUSION IN DIABETIC RATS [J].
BANK, N ;
MOWER, P ;
AYNEDJIAN, HS ;
WILKES, BM ;
SILVERMAN, S .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 256 (06) :F1000-F1006