Protein tyrosine phosphatase-1B in diabetes

被引:132
作者
Kennedy, BP [1 ]
Ramachandran, C [1 ]
机构
[1] Merck Frosst Canada Inc, Merck Frosst Ctr Therapeut Res, Dept Biochem & Mol Biol, Pointe Claire, PQ H9R 4P8, Canada
关键词
PTP-1B; diabetes; insulin signaling; obesity;
D O I
10.1016/S0006-2952(00)00305-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A role for protein tyrosine phosphatases in the negative regulation of insulin signaling and a putative involvement in the insulin resistance associated with type 2 diabetes have been postulated since their discovery. The recent demonstration that mice lacking the protein tyrosine phosphatase-1B (PTP-1B) have enhanced insulin sensitivity validates this. Furthermore, when fed a high fat diet, these mice maintained insulin sensitivity and were resistant to obesity, suggesting that inhibition of PTP-1B activity could be a novel way of treating type 2 diabetes and obesity. This commentary reviews our current knowledge of PTP-1B in insulin signaling and its role in diabetes and discusses the development of potent and selective PTP-1B inhibitors. BIOCHEM PHARMACOL 60;7:877-883, 2000. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:877 / 883
页数:7
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