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尽管用醛糖还原酶抑制剂治疗,链脲佐菌素诱导的糖尿病大鼠仍出现肾小球基底膜增厚。

Glomerular basement membrane thickening in streptozotocin diabetic rats despite treatment with an aldose reductase inhibitor.

作者信息

Osterby R, Gundersen H J

机构信息

Electron Microscopic Diabetes Research Laboratory, Aarhus University, Denmark.

出版信息

J Diabet Complications. 1989 Jul-Sep;3(3):149-53. doi: 10.1016/0891-6632(89)90037-8.

Abstract

This study concerns the possible prevention of glomerular basement membrane thickening in experimental diabetes by an aldose reductase inhibitor (ARI), Statil. ARI added to the chow was given to streptozotocin diabetic rats over a period of 6 months. Reference groups were control rats and diabetic rats on the same chow without ARI. The diabetic rats were given insulin two or three times a week, and blood glucose was measured monthly before insulin injections. There was a marked difference in the occurrence of cataracts between the two diabetic groups. ARI treated rats tended to have lower blood glucose than the diabetic reference group, but the difference was not significant. At the termination of the experiment, the left kidney was perfusion fixed, weighed, and prepared for light and electron microscopy. Systematic random sampling from the entire kidney was performed to obtain light microscopic visual fields and ultrathin sections from two glomeruli. Mean glomerular volume was estimated by light microscopy, and glomerular basement membrane thickness, by electron microscopy. Basement membrane thickness was significantly increased in untreated diabetic rats (174 nm, SD = 4.5 nm) as compared to that of controls (Mean: 154 nm, SD = 11.0 nm), and was even more so in ARI treated rats (187 nm, SD = 18.7 nm), although the ARI treated rats showed less renal and glomerular hypertrophy than did untreated diabetic rats. In conclusion, the ARI treatment over an experimental period of 6 months attenuated diabetic renal and glomerular hypertrophy, but had no effect at all on diabetic glomerular basement membrane thickening.

摘要

本研究关注醛糖还原酶抑制剂(ARI)Statil对实验性糖尿病中肾小球基底膜增厚的可能预防作用。将添加了ARI的食物喂给链脲佐菌素诱导的糖尿病大鼠,持续6个月。参照组为食用相同食物但未添加ARI的对照大鼠和糖尿病大鼠。糖尿病大鼠每周注射胰岛素两到三次,每月在注射胰岛素前测量血糖。两组糖尿病大鼠在白内障发生率上存在显著差异。接受ARI治疗的大鼠血糖往往低于糖尿病参照组,但差异不显著。实验结束时,对左肾进行灌注固定、称重,并制备用于光镜和电镜检查的样本。从整个肾脏进行系统随机抽样,以获取光镜视野和两个肾小球的超薄切片。通过光镜估计平均肾小球体积,通过电镜测量肾小球基底膜厚度。与对照组(平均值:154nm,标准差 = 11.0nm)相比,未治疗的糖尿病大鼠的基底膜厚度显著增加(174nm,标准差 = 4.5nm),而接受ARI治疗的大鼠的基底膜厚度增加得更多(187nm,标准差 = 18.7nm),尽管接受ARI治疗的大鼠的肾脏和肾小球肥大程度低于未治疗的糖尿病大鼠。总之,在6个月的实验期内,ARI治疗减轻了糖尿病性肾和肾小球肥大,但对糖尿病性肾小球基底膜增厚完全没有作用。

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