Sima Anders A F
Department of Pathology, Wayne State University, Detroit, MI 48201, USA.
Front Biosci. 2008 May 1;13:4809-16. doi: 10.2741/3040.
Diabetic neuropathy and its underlying pathogenesis are reviewed. It has been documented for some time that diabetic neuropathy differs in both human and experimental type 1 versus type 2 diabetes. Such differences are accounted for by impaired insulin action and signal transduction in type 1 diabetes, whereas hyperglycemia per se contributes equally to neuropathy in the two types of diabetes. Such differences in basic initiating factors and pathogenesis translate into differences in the functional and structural expressions of neuropathy in type 1 and type 2 diabetes. Type 1 neuropathy shows a more rapid progression with more severe functional and structural changes. Several experimental mono-therapies have been tested over the last decades which unfortunately have not been efficacious. Therefore discrepancies in underlying pathogenetic mechanisms in the two types of diabetic neuropathy will have to be taken into account in the design of future therapies, which should target several key pathogenetic mechanisms. Therapies that meet these criteria include replacement of acetyl-L-carnitine and replenishment of C-peptide in type 1 diabetic neuropathy.
本文对糖尿病神经病变及其潜在发病机制进行了综述。一段时间以来,已有文献记载,糖尿病神经病变在人类以及实验性1型和2型糖尿病中均有所不同。1型糖尿病中胰岛素作用和信号转导受损导致了这些差异,而高血糖本身在两种类型的糖尿病中对神经病变的影响程度相当。这些基本起始因素和发病机制的差异导致了1型和2型糖尿病神经病变在功能和结构表现上的差异。1型神经病变进展更快,功能和结构变化更严重。在过去几十年中,已经对几种实验性单一疗法进行了测试,但遗憾的是这些疗法均未取得疗效。因此,在设计未来疗法时必须考虑两种类型糖尿病神经病变潜在发病机制的差异,未来疗法应针对几种关键发病机制。符合这些标准的疗法包括在1型糖尿病神经病变中补充乙酰-L-肉碱和补充C肽。