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代谢型谷氨酸受体作为新型抗抑郁药的潜在靶点。

mGlu receptors as potential targets for novel antidepressants.

机构信息

Research Headquarters, Taisho Pharmaceutical Co., Ltd., 1-403 Yoshino-cho, Kita-ku, Saitama, Saitama 331-9530, Japan.

Research Headquarters, Taisho Pharmaceutical Co., Ltd., 1-403 Yoshino-cho, Kita-ku, Saitama, Saitama 331-9530, Japan.

出版信息

Curr Opin Pharmacol. 2018 Feb;38:24-30. doi: 10.1016/j.coph.2018.02.001. Epub 2018 Feb 24.

Abstract

Ever since the discovery of the rapid and sustained antidepressant effect of ketamine, a non-competitive N-methyl-d-aspartate receptor antagonist, agents acting on the glutamatergic system have been explored for their potential as novel antidepressants. Among the glutamategic system, metabotropic glutamate (mGlu) receptors, which play important roles in regulating glutamate transmission, have recently gained much attention as potential targets for the development of novel antidepressants. Of these, the antidepressant effects of agents acting on the mGlu2/3 receptor and mGlu5 receptor have been well characterized in several animal models. Moreover, the synaptic and neural mechanisms underlying the antidepressant actions of mGlu2/3 receptor and mGlu5 receptor antagonists have been elucidated, in comparison with those of ketamine. In contrast, the roles of the group III mGlu receptors, including mGlu4 and mGlu7, in depression remain to be investigated further by using selective ligands for each receptor.

摘要

自从发现非竞争性 N-甲基-D-天冬氨酸受体拮抗剂氯胺酮具有快速和持续的抗抑郁作用以来,人们一直在探索作用于谷氨酸能系统的药物,以寻找新的抗抑郁药物的潜力。在谷氨酸能系统中,代谢型谷氨酸 (mGlu) 受体在调节谷氨酸传递中发挥着重要作用,最近作为新型抗抑郁药物开发的潜在靶点备受关注。其中,作用于 mGlu2/3 受体和 mGlu5 受体的药物的抗抑郁作用已在多种动物模型中得到很好的描述。此外,与氯胺酮相比,mGlu2/3 受体和 mGlu5 受体拮抗剂抗抑郁作用的突触和神经机制已经阐明。相比之下,使用每种受体的选择性配体,进一步研究包括 mGlu4 和 mGlu7 在内的 III 组 mGlu 受体在抑郁症中的作用仍有待研究。

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