Potential New Treatments for Diabetic Kidney Disease

被引:10
|
作者
Kania, Deanna S. [1 ,2 ]
Smith, Cory T. [1 ,3 ]
Nash, Christy L. [1 ,4 ]
Gonzalvo, Jasmine D. [1 ]
Bittner, Andrea [1 ]
Shepler, Brian M. [1 ]
机构
[1] Purdue Univ, Coll Pharm, W Lafayette, IN 47907 USA
[2] RL Roudebush VA Med Ctr, Indianapolis, IN 46202 USA
[3] Floyd Mem Hosp, New Albany, IN 47150 USA
[4] Mathes Pharm, Ctr Diabet, New Albany, IN 47150 USA
关键词
Pentoxifylline; Bardoxolone; Pirfenidone; Doxycycline; Diabetic kidney disease; RECEPTOR ANTAGONIST PALOSURAN; GROWTH-FACTOR-BETA; ALBUMIN EXCRETION RATE; PROTEIN-KINASE-C; UROTENSIN-II; BARDOXOLONE METHYL; VITAMIN-D; MESANGIAL EXPANSION; URINARY ENDOTHELIN; ORAL ADSORBENT;
D O I
10.1016/j.mcna.2012.10.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetic kidney disease is a complex pathologic process that involves many biochemical associations. As our understanding of this processes deepens, potential new targets for drug therapy become apparent. There are several mechanisms by which medications may be able to ihhibit or slow the progression of kidney disease. Existing medications and entirely new compounds have been studied in human subjects that have antag-brotic and antioxidant effects as well as the ability to bind with and antagonize specific receptors known to contribute to the deleterious effects observed in diabetic kidney disease patients. While most potential new drug therapies remain highly experimental, there is a growing body of data from clinical trials show that many new drugs may eventually lead to new standards for drug treatment in diabetic kidney disease. Potential new drug therapies discussed include antifibrotic agents, antioxidant agents, ET-a receptor antagonists and other compounds with non-specific or multi-faceted mechanisms of action such as paricalcitol, ruboxistaurin, palosuran, allopurinol, and fasudil.
引用
收藏
页码:115 / +
页数:21
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