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代谢型谷氨酸受体7(mGluR7)作为治疗精神兴奋剂依赖的靶点

Metabotropic Glutamate Receptor 7 (mGluR7) as a Target for the Treatment of Psychostimulant Dependence.

作者信息

Li Xia, Markou Athina

机构信息

Department of Psychiatry, M/C 0603, School of Medicine, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0603, USA.

出版信息

CNS Neurol Disord Drug Targets. 2015;14(6):738-44. doi: 10.2174/1871527314666150529145332.

Abstract

Although few medications have been approved by the U.S. Food and Drug Administration (FDA) to assist people to quit tobacco smoking, there are no FDA-approved medications to treat dependence on other psychostimulant drugs, such as cocaine. The motivation to maintain psychostimulant drug seeking and self-administration involves alterations in glutamatergic neurotransmission. Thus, medications that modulate glutamate transmission may be effective treatments for psychostimulant dependence. One presynaptic inhibitory glutamate receptor that critically regulates glutamate transmission is the metabotropic glutamate 7 receptor (mGluR7). This review summarizes nonhuman experimental animal data that indicate a critical role for mGluR7 in drug-taking and drug-seeking behaviors for the psychostimulants cocaine and nicotine. AMN082, the only commercially available allosteric receptor agonist, has been used to investigate the role of mGluR7 in psychostimulant dependence. Systemic administration or microinjection of AMN082 into brain sites within the mesocorticolimbic system decreased self-administration and reinstatement of both cocaine and nicotine seeking. In vivo microdialysis results indicated that a nucleus accumbens-ventral pallidum γ-aminobutyric acid-ergic mechanism may underlie AMN082-induced antagonism of the reinforcing effects of cocaine, whereas a glutamate mGlu2/3 receptor mechanism underlies the AMN082-induced blockade of cocaine seeking. These findings indicate an important role for mGluR7 in mesolimbic areas in modulating the reinforcing effects of psychostimulant drugs, such as nicotine and cocaine, and the conditioned behaviors associated with drugs of abuse. Thus, selective mGluR7 agonists or positive allosteric modulators may have the potential to treat psychostimulant dependence.

摘要

尽管美国食品药品监督管理局(FDA)仅批准了少数几种药物来帮助人们戒烟,但尚无FDA批准的用于治疗对其他精神刺激药物(如可卡因)成瘾的药物。维持对精神刺激药物的寻求和自我给药的动机涉及谷氨酸能神经传递的改变。因此,调节谷氨酸传递的药物可能是治疗精神刺激药物成瘾的有效方法。一种对谷氨酸传递起关键调节作用的突触前抑制性谷氨酸受体是代谢型谷氨酸7受体(mGluR7)。这篇综述总结了非人类实验动物数据,这些数据表明mGluR7在精神刺激药物可卡因和尼古丁的用药及觅药行为中起关键作用。AMN082是唯一一种可商购的变构受体激动剂,已被用于研究mGluR7在精神刺激药物成瘾中的作用。全身给药或向中脑皮质边缘系统内的脑区微量注射AMN082,均可减少可卡因和尼古丁的自我给药及觅药行为的恢复。体内微透析结果表明,伏隔核-腹侧苍白球γ-氨基丁酸能机制可能是AMN082诱导的可卡因强化作用拮抗的基础,而谷氨酸mGlu2/3受体机制是AMN082诱导的可卡因觅药行为阻断的基础。这些发现表明mGluR7在边缘中脑区域对调节精神刺激药物(如尼古丁和可卡因)的强化作用以及与滥用药物相关的条件性行为中起重要作用。因此,选择性mGluR7激动剂或正变构调节剂可能具有治疗精神刺激药物成瘾的潜力。

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