神经药理学报››2013,Vol. 3››Issue (1): 48-64.
• 综述 •上一篇
邱艳艳1,2，李俊旭1，何小华2
出版日期:2013-02-26发布日期:2014-06-27通讯作者:李俊旭，男，博士，助理教授；研究方向：行为药理学；Tel: +01-716-8292482， Email: junxuli@buffalo.edu基金资助:
美国国立卫生研究院NIH (1R01DA034806, 1R21DA033426)
QIU Yan-yan1,2, LI Jun-xu1, HE Xiao-hua2
Online:2013-02-26Published:2014-06-27Contact:李俊旭，男，博士，助理教授；研究方向：行为药理学；Tel: +01-716-8292482， Email: junxuli@buffalo.eduSupported by:
美国国立卫生研究院NIH (1R01DA034806, 1R21DA033426)
摘要：咪唑啉I2受体是一种非G蛋白偶联受体，其生理功能及临床意义目前尚不十分清楚。近年大量研究表明I2受体通过相关配体介导多种行为学效应。激活咪唑啉I2受体可能产生镇痛、抗抑郁、调节阿片受体功能、神经元保护等多种药理学作用。本文着重介绍了I2受体的分布、细胞定位、分子结构、信号转导、内源性配体和选择性配体及其相关神经药理学效应的研究进展。
邱艳艳，李俊旭，何小华.咪唑啉I2受体神经药理学研究进展[J]. 神经药理学报, 2013, 3(1): 48-64.
QIU Yan-yan, LI Jun-xu, HE Xiao-hua.The Neuropharmacology of Imiazoline-I2Receptors[J]. Acta Neuropharmacologica, 2013, 3(1): 48-64.
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