Oxidative injury and neuropathy in diabetes and impaired glucose tolerance

被引:114
作者
Russell, James W. [1 ,2 ,3 ]
Berent-Spillson, Alison [5 ]
Vincent, Andrea M. [4 ]
Freimann, Catherine L. [6 ]
Sullivan, Kelli A. [4 ]
Feldman, Eva L. [4 ]
机构
[1] Univ Maryland, Dept Neurol, Baltimore, MD 21201 USA
[2] Univ Maryland, Dept Anat & Neurobiol, Baltimore, MD 21201 USA
[3] Vet Affairs Med Ctr, Baltimore, MD USA
[4] Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Mol & Behav Neurosci Inst, Ann Arbor, MI 48109 USA
[6] Novartis Pharmaceut, E Hanover, NJ USA
关键词
neuropathy; diabetes; impaired glucose tolerance; oxidative; stress; axons; dorsal root ganglia; schwann cells;
D O I
10.1016/j.nbd.2008.02.013
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Clinical studies suggest that impaired glucose tolerance (IGT) is associated with the development of neuropathy. The aim of the current study was to determine if neuropathy developed in the female Zucker Diabetic Fatty (ZDF) rat, an animal model of IGT and type 2 diabetes. The ZDF rat develops impaired glucose tolerance (IGT) when fed a control diet, and frank diabetes when fed a high fat diet. Following 10 weeks of hyperglycemia, sensory nerve action potentials (SNAP) and compound motor action potentials (CMAP) were reduced and sensory conduction velocities were slowed (distal > proximal) in the tail and hind limb in ZDF animals with IGT and frank diabetes (p < 0.01). Neuropathy was coupled with evidence of increased reactive oxygen species (ROS) and cellular injury in dorsal root ganglion (DRG) neurons from IGT animals. Our study supports the hypothesis that neuropathy develops in an animal model of IGT and is associated with evidence of oxidative injury in DRG and peripheral nerves. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:420 / 429
页数:10
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