醛糖还原酶
姜黄素
山梨醇
醛还原酶
醛糖还原酶抑制剂
生物化学
化学
抗氧化剂
非竞争性抑制
还原酶
体内
酶
多元醇途径
药理学
生物
生物技术
作者
Puppala Muthenna,Palla Suryanarayana,Shravan Kumar Gunda,Jonathan Mark Petrash,G. Bhanuprakash Reddy
出处
期刊:FEBS Letters
[Wiley]
日期:2009-10-20
卷期号:583 (22): 3637-3642
被引量:109
标识
DOI:10.1016/j.febslet.2009.10.042
摘要
Accumulation of intracellular sorbitol due to increased aldose reductase (ALR2) activity has been implicated in the development of various secondary complications of diabetes. In this study we show that curcumin inhibits ALR2 with an IC(50) of 10 microM in a non-competitive manner, but is a poor inhibitor of closely-related members of the aldo-keto reductase superfamily, particularly aldehyde reductase. Results from molecular docking studies are consistent with the pattern of inhibition of ALR2 by curcumin and its specificity. Moreover, curcumin is able to suppress sorbitol accumulation in human erythrocytes under high glucose conditions, demonstrating an in vivo potential of curcumin to prevent sorbitol accumulation. These results suggest that curcumin holds promise as an agent to prevent or treat diabetic complications.
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