New Insight into the Molecular Drug Target of Diabetic Nephropathy

被引:24
作者
Soetikno, Vivian [1 ]
Arozal, Wawaimuli [1 ]
Louisa, Melva [1 ]
Setiabudy, Rianto [1 ]
机构
[1] Univ Indonesia, Fac Med, Dept Pharmacol & Therapeut, Jakarta 10430, Indonesia
关键词
PROTEIN-KINASE-C; ANGIOTENSIN-CONVERTING ENZYME; GLYCATION END-PRODUCTS; RENAL LIPID-METABOLISM; OXIDATIVE STRESS; RENIN-ANGIOTENSIN; LONG-TERM; TGF-BETA; BARDOXOLONE METHYL; MAMMALIAN TARGET;
D O I
10.1155/2014/968681
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetic nephropathy (DN) lowered quality of life and shortened life expectancy amongst those affected. Evidence indicates interaction between advanced glycation end products (AGEs), activated protein kinase C (PKC) and angiotensin II exacerbate the progression of DN. Inhibitors of angiotensin-converting enzyme (ACEIs), renin angiotensin aldosterone system (RAAS), AGEs, and PKC have been tested for slowing down the progression of DN. The exact molecular drug targets that lead to the amelioration of renal injury in DN are not well understood. This review summarizes the potential therapeutic targets, based on putative mechanism in the progression of the disease.
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页数:9
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