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多元醇途径活性与肌醇代谢。糖尿病性神经病变发病机制中的一种推测关系。

Polyol pathway activity and myo-inositol metabolism. A suggested relationship in the pathogenesis of diabetic neuropathy.

作者信息

Finegold D, Lattimer S A, Nolle S, Bernstein M, Greene D A

出版信息

Diabetes. 1983 Nov;32(11):988-92. doi: 10.2337/diab.32.11.988.

Abstract

Two major metabolic perturbations, increased polyol (sorbitol) pathway activity and reduced tissue myo-inositol content, are induced in peripheral nerve by hyperglycemia. Although they are commonly invoked as alternative biochemical pathogenetic mechanisms for diabetic neuropathy, their possible interrelationship has never been adequately explored. Therefore, we studied the effect of polyol pathway blockade with sorbinil, a specific inhibitor of aldose reductase, on nerve myo-inositol content in acutely streptozotocin-diabetic rats. Sorbinil administration completely prevented the fall in nerve myo-inositol, thereby implicating increased polyol pathway activity as a likely factor in the fall in nerve myo-inositol content in experimental diabetes.

摘要

高血糖会在外周神经中引发两种主要的代谢紊乱,即多元醇(山梨醇)途径活性增加和组织中肌醇含量降低。尽管它们通常被认为是糖尿病性神经病变的替代生化致病机制,但其可能的相互关系从未得到充分探究。因此,我们研究了醛糖还原酶的特异性抑制剂索比尼尔阻断多元醇途径对急性链脲佐菌素诱导的糖尿病大鼠神经肌醇含量的影响。给予索比尼尔可完全防止神经肌醇含量下降,从而表明多元醇途径活性增加可能是实验性糖尿病中神经肌醇含量下降的一个因素。

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