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糖尿病治疗的新靶点:糖原合酶激酶-3抑制剂的研究进展

[A new target for diabetes therapy: advances in the research of glycogen synthase kinase-3 inhibitors].

作者信息

Liu Shuai-nan, Shen Zhu-fang

机构信息

Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.

出版信息

Yao Xue Xue Bao. 2007 Dec;42(12):1227-31.

PMID:18338632
Abstract

Glycogen synthase kinase-3 (GSK-3) is a serine/threonine kinase, originally identified as a protein kinase by its ability to phosphorylate and inactivate glycogen synthase. It was found that the overexpression of GSK-3 is associated with some diseases, such as diabetes, Alzheimer disease and other neurodegenerative diseases. Some pharmacological inhibitors of GSK-3 have been demonstrated to mimic insulin signaling, adjust glycogen synthesis and glucose metabolism, and improve insulin resistance. So GSK-3 inhibitors are realized as a new approach of treating diabetes. This review summarizes current advances in research of GSK-3 inhibitors as a new therapeutic approach for diabetes.

摘要

糖原合酶激酶-3(GSK-3)是一种丝氨酸/苏氨酸激酶,最初因其能够磷酸化糖原合酶并使其失活而被鉴定为一种蛋白激酶。研究发现,GSK-3的过表达与一些疾病相关,如糖尿病、阿尔茨海默病和其他神经退行性疾病。一些GSK-3的药理学抑制剂已被证明可模拟胰岛素信号传导,调节糖原合成和葡萄糖代谢,并改善胰岛素抵抗。因此,GSK-3抑制剂被视为一种治疗糖尿病的新方法。本文综述了GSK-3抑制剂作为糖尿病新治疗方法的研究进展。

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