福斯可林通过抑制醛糖还原酶和晚期糖基化终产物的形成来减轻糖尿病肾病

S. Damera, Ajmera Rr, Ciddi
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引用次数: 0

摘要

目的:多种机制,包括多元醇途径以及醛糖还原酶(AR)和晚期糖基化终产物(AGE)形成的复杂整合范式,与糖尿病肾病的发病机制有关。方法:本研究旨在研究著名抗氧化剂福斯克林对链脲佐菌素诱导的大鼠糖尿病肾病的治疗作用。通过检测肾功能关键指标及肾脏形态学变化,探讨福斯柯林的作用。此外,与标准AR抑制剂非达司他比较了福斯克林对age形成、AR抑制和脂质过氧化的影响。结果:茯苓醇提物和茯苓素均能显著(P<0.05)降低糖尿病大鼠血糖水平、尿蛋白排泄量、血清肌酐和尿素氮。糖尿病大鼠给予福斯克林可降低肾脏脂质过氧化物和硝酸盐水平,并减少AGEs的形成。此外,还发现Forskolin可抑制肾脏AR活性。结论:因此,本研究的结果强调了福斯克林作为糖尿病并发症(如肾病)的潜在治疗剂的潜力。*通信对象:印度特伦加纳邦瓦兰加尔市Kakatiya大学药学院药学教授Ciddi Veeresham,电子邮件:ciddiveereham@yahoo.co.in
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Forskolin alleviates diabetic nephropathy via inhibition of aldose reductase and advanced glycation end products formation
Objectives: Various mechanisms including polyol pathway along with a complex integrating paradigm with Aldose reductase (AR) and advanced glycation end products (AGE) formation have been implicated in the pathogenesis of diabetic nephropathy. Methods: The present study was aimed at investigating a well-known antioxidant, Forskolin for its therapeutic role in streptozotocin-induced diabetic nephropathy in rats. The effect of Forskolin was investigated by assessing the key markers of kidney function along with the morphological changes in the kidney. Further, the effect of Forskolin on the formation of AGEs and AR inhibition and lipid peroxidation was compared with that of a standard AR inhibitor, fidarestat. Results: The results revealed that Coleus forskohlii methanolic extract and Forskolin significantly (P<0.05) decreased the blood glucose levels, urinary protein excretion, serum creatinine and blood urea nitrogen in diabetic rats. Administration of Forskolin to diabetic rats decreased kidney lipid peroxides and nitrate levels along with decrease in AGEs formation. In addition, Forskolin was found to inhibit kidney AR activity. Conclusion: Thus, the results obtained in this study underline the potential of Forskolin as a possible therapeutic agent against diabetic complications such as nephropathy. *Correspondence to: Ciddi Veeresham, Professor of Pharmacy, University College of Pharmaceutical Sciences, Kakatiya University, Warangal, Telangana, India 506009, E-mail: ciddiveereham@yahoo.co.in
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