Glucose-induced oxidative stress and programmed cell death in diabetic neuropathy

被引:179
作者
Greene, DA
Stevens, MJ
Obrosova, I
Feldman, EL
机构
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Michigan Diabet Res & Training Ctr, Ann Arbor, MI 48109 USA
关键词
glucose; diabetic neuropathy; programmed cell death;
D O I
10.1016/S0014-2999(99)00356-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The Diabetes Control and Complications Trial (DCCT) established the importance of hyperglyemia and other consequences of insulin deficiency in the pathogenesis of diabetic neuropathy, but the precise mechanisms by which metabolic alterations produce peripheral nerve fiber damage and loss remain unclear. Emerging data from human and animal studies suggest that glucose-derived oxidative stress may play a central role, linking together many of the other currently invoked pathogenetic mechanisms such as the aldose reductase and glycation pathways, vascular dysfunction, and impaired neurotrophic support. These relationships suggest combinations of pharmacological interventions that may synergistically protect the peripheral nervous system (PNS) against the metabolic derangements of diabetes mellitus. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:217 / 223
页数:7
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