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糖原合成酶激酶-3是双相情感障碍治疗干预中一个可行的潜在靶点。

GSK-3 is a viable potential target for therapeutic intervention in bipolar disorder.

作者信息

Rowe Michael K, Wiest Charlotte, Chuang De-Maw

机构信息

Molecular Neurobiology Section, Mood and Anxiety Disorders Program, National Institute of Mental Health, National Institutes of Health, Building 10, Room 4C206, 10 Center Drive, MSC 1363, Bethesda, MD 20892-1363, USA.

出版信息

Neurosci Biobehav Rev. 2007;31(6):920-31. doi: 10.1016/j.neubiorev.2007.03.002. Epub 2007 Mar 15.

Abstract

Bipolar disorder is a serious psychiatric condition that has been treated for over 50 years with lithium. Lithium is a well established glycogen synthase kinase-3 (GSK-3) inhibitor, suggesting that manipulating GSK-3 may have therapeutic value in treating bipolar disorder. GSK-3 is regulated by a wide variety of mechanisms including phosphorylation, binding with protein complexes, phosphorylation state of its substrates, cellular localization and autoregulation, thus providing a wide number of potential therapeutic mechanisms. Mounting evidence suggests that GSK-3 regulation can be used to manage bipolar disorder symptoms. Although GSK-3 mutations have not been detected amongst the general bipolar population, they have been correlated with females with bipolar II and most of the drugs used for successful bipolar disorder treatment regulate GSK-3. These drugs produce a weak anti-depressant-like and a strong anti-mania-like effect in a wide range of animal models tested, mirroring their utility in treating bipolar disorder symptoms. Taken together, the evidence suggests that targeting GSK-3 may be a means to control the symptoms of bipolar disorder.

摘要

双相情感障碍是一种严重的精神疾病,使用锂盐治疗已有50多年历史。锂盐是一种公认的糖原合酶激酶-3(GSK-3)抑制剂,这表明调控GSK-3可能对双相情感障碍的治疗具有重要价值。GSK-3受多种机制调控,包括磷酸化、与蛋白复合物结合、底物的磷酸化状态、细胞定位及自身调节,因此存在众多潜在的治疗机制。越来越多的证据表明,调控GSK-3可用于控制双相情感障碍的症状。虽然在普通双相情感障碍患者群体中未检测到GSK-3突变,但这些突变与双相II型障碍女性患者相关,并且大多数成功用于双相情感障碍治疗的药物都能调控GSK-3。在广泛的动物模型测试中,这些药物产生了微弱的抗抑郁样效应和强烈的抗躁狂样效应,这与它们在治疗双相情感障碍症状方面的效用相符。综上所述,有证据表明靶向GSK-3可能是控制双相情感障碍症状的一种方法。

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