Phrenic nerve diabetic neuropathy in rats: unmyelinated fibers morphometry

被引:13
|
作者
Fazan, Valeria Paula S. [1 ,2 ]
Rodrigues Filho, Omar A. [3 ]
Jordao, Caroline E. R. [1 ]
Moore, Kenneth C. [2 ]
机构
[1] Univ Sao Paulo, Sch Med Ribeirao Preto, Dept Surg & Anat, BR-14049900 Ribeirao Preto, Brazil
[2] Univ Iowa, Cent Microscopy Res Facil, Iowa City, IA USA
[3] Univ Fed Triangulo Mineiro, Dept Biol Sci, Uberaba, MG, Brazil
基金
巴西圣保罗研究基金会;
关键词
experimental diabetes; insulin treatment; morphometry; phrenic nerve; unmyelinated fiber; MYELINATED FIBERS; PERIPHERAL-NERVES; RENAL NERVES; ABNORMALITIES; MORPHOLOGY; PATHOLOGY; MELLITUS; THERAPY; MODEL;
D O I
10.1111/j.1529-8027.2009.00223.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We have demonstrated that phrenic nerves' large myelinated fibers in streptozotocin (STZ)-induced diabetic rats show axonal atrophy, which is reversed by insulin treatment. However, studies on structural abnormalities of the small myelinated and the unmyelinated fibers in the STZ-model of neuropathy are limited. Also, structural changes in the endoneural vasculature are not clearly described in this model and require detailed study. We have undertaken morphometric studies of the phrenic nerve in insulin-treated and untreated STZ-diabetic rats and non-diabetic control animals over a 12-week period. The presence of neuropathy was assessed by means of transmission electron microscopy, and morphometry of the unmyelinated fibers was performed. The most striking finding was the morphological evidence of small myelinated fiber neuropathy due to the STZ injection, which was not protected or reversed by conventional insulin treatment. This neuropathy was clearly associated with severe damage of the endoneural vessels present on both STZ groups, besides the insulin treatment. The STZ-diabetes model is widely used to investigate experimental diabetic neuropathies, but few studies have performed a detailed assessment of either unmyelinated fibers or capillary morphology in this animal model. The present study adds useful information for further investigations on the ultrastructural basis of nerve function in diabetes.
引用
收藏
页码:137 / 145
页数:9
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