Chakrabarti S, Sima A A
Department of Pathology, University of Manitoba, Winnipeg, MB, Canada.
Diabetes Res Clin Pract. 1992 Apr;16(1):13-7. doi: 10.1016/0168-8227(92)90130-j.
A polyol-pathway related perturbation of myo-inositol metabolism has been invoked in the pathogenesis of diabetic complications, including retinal microvasculopathy. Previous studies have demonstrated a beneficiary effect of aldose reductase inhibition on basement membrane thickening of retinal microvessels in diabetic animals. In the present study we demonstrate a significant but partial effect on basement membrane thickening following myo-inositol supplementation. Qualitative structural changes, such as nodular swellings, fibrillar changes and basement membrane projections were not effected by myo-inositol supplementation, suggesting that although abnormal myo-inositol tissue levels may play a role in basement membrane thickening, other factors may be of primary pathogenetic importance.
多元醇通路相关的肌醇代谢紊乱已被认为与糖尿病并发症(包括视网膜微血管病变)的发病机制有关。先前的研究表明,醛糖还原酶抑制对糖尿病动物视网膜微血管基底膜增厚具有有益作用。在本研究中,我们证明补充肌醇后对基底膜增厚有显著但部分的影响。补充肌醇并未影响结节状肿胀、纤维状改变和基底膜突起等定性结构变化,这表明尽管肌醇组织水平异常可能在基底膜增厚中起作用,但其他因素可能在发病机制中更为重要。