Giannoukakis Nick
University of Pittsburgh School of Medicine, Department of Pathology and Immunology, Diabetes Institute, Rangos Research Center, 3460 Fifth Avenue, Pittsburgh, PA 15213, USA.
Expert Opin Investig Drugs. 2008 Apr;17(4):575-81. doi: 10.1517/13543784.17.4.575.
There are currently very few drugs available to directly treat diabetic complications. Those that are indicated clinically provide symptomatic relief and do not address the underlying biochemical problems. The involvement of the sorbitol pathway in complications has provided mechanistic insights into the biochemistry of complications and the key enzyme, aldose reductase, has become an attractive pharmacologic target.
Among the aldose reductase inhibitors, the most promising is ranirestat. This review outlines the studies with ranirestat and compares its efficacy with other similar inhibitors.
A survey of in vitro and in vivo studies was conducted, and with publicly available data from clinical trials, ranirestat efficacy was compared with other similar agents.
RESULTS/CONCLUSION: Ranirestat is safe, exhibits some efficacy and is perhaps the only agent advanced enough in clinical trials to warrant further consideration for diabetic complications.
目前可直接用于治疗糖尿病并发症的药物非常少。临床应用的药物只能缓解症状,无法解决潜在的生化问题。山梨醇途径在并发症中的作用为并发症的生物化学机制提供了见解,关键酶醛糖还原酶已成为一个有吸引力的药物靶点。
在醛糖还原酶抑制剂中,最有前景的是雷纳司他。本综述概述了雷纳司他的研究,并将其疗效与其他类似抑制剂进行比较。
对体外和体内研究进行了调查,并利用临床试验的公开数据,将雷纳司他的疗效与其他类似药物进行比较。
结果/结论:雷纳司他安全,有一定疗效,可能是唯一在临床试验中进展到足以值得进一步考虑用于治疗糖尿病并发症的药物。