Yang Hong-Ju, Zhang Hai-Ying, Bi Guo-Hua, He Yi, Gao Jun-Tao, Xi Zheng-Xiong
Molecular Targets and Medications Discovery Branch, Intramural Research Program, National Institute on Drug Abuse, Baltimore, MD 21224, USA.
Molecular Targets and Medications Discovery Branch, Intramural Research Program, National Institute on Drug Abuse, Baltimore, MD 21224, USA.
Cell Rep. 2017 Jul 11;20(2):319-332. doi: 10.1016/j.celrep.2017.06.046.
Cocaine users show reduced expression of the metabotropic glutamate receptor (mGluR2), but it is not clear whether this is a predisposing trait for addiction or a consequence of drug exposure. In this study, we found that a nonsense mutation at the mGluR2 gene decreased mGluR2 expression and altered the seeking and taking of cocaine. mGluR2 mutant rats show reduced sensitivity to cocaine reward, requiring more cocaine to reach satiation when it was freely available and ceasing their drug-seeking behavior sooner than controls when the response requirement was increased. mGluR2 mutant rats also show a lower propensity to relapse after a period of cocaine abstinence, an effect associated with reduced cocaine-induced dopamine and glutamate overflow in the nucleus accumbens. These findings suggest that mGluR2 polymorphisms or reduced availability of mGluR2 might be risk factors for the initial development of cocaine use but could actually protect against addiction by reducing sensitivity to cocaine reward.
可卡因使用者的代谢型谷氨酸受体(mGluR2)表达降低,但尚不清楚这是成瘾的易患特质还是药物暴露的结果。在本研究中,我们发现mGluR2基因的一个无义突变降低了mGluR2的表达,并改变了对可卡因的寻觅和摄取。mGluR2突变大鼠对可卡因奖赏的敏感性降低,当可卡因可自由获取时,需要更多的可卡因才能达到饱足状态,并且当反应要求增加时,它们比对照大鼠更早停止觅药行为。mGluR2突变大鼠在一段可卡因戒断期后的复发倾向也较低,这种效应与伏隔核中可卡因诱导的多巴胺和谷氨酸溢出减少有关。这些发现表明,mGluR2基因多态性或mGluR2可用性降低可能是可卡因使用初始发展的风险因素,但实际上可能通过降低对可卡因奖赏的敏感性来预防成瘾。