Kufahl Peter R, Nemirovsky Natali E, Watterson Lucas R, Zautra Nicholas, Olive M Foster
Department of Psychology, Arizona State University, Tempe, AZ, 85287-1104, USA.
F1000Res. 2013 Mar 12;2:84. doi: 10.12688/f1000research.2-84.v1. eCollection 2013.
We investigated the role of metabotropic glutamate receptor type 5 (mGluR5) in methamphetamine-induced behavioral sensitization. The mGluR5 positive allosteric modulator (3-cyano-N-(1,3-diphenyl-1H-pyrazol-5-yl) benzamide (CDPPB) and negative allosteric modulator fenobam were tested in separate experiments. Sprague-Dawley rats were repeatedly injected with 1 mg/kg methamphetamine or saline, and then given a locomotor challenge test using a dose of 0.5 mg/kg methamphetamine. Prior to the challenge test session, rats were injected with CDPPB, fenobam, or a vehicle. Doses from previous studies showed reduced drug-conditioned behavior; however in this study neither CDPPB nor fenobam pretreatment resulted in an altered expression of behavioral sensitization, indicating a lack of mGluR5 involvement in sensitized methamphetamine-induced locomotion. Additionally, the high dose (30 mg/kg) of fenobam resulted in decreased methamphetamine-induced locomotion in rats regardless of drug exposure history, which suggests evidence of nonspecific behavioral inhibition.
我们研究了代谢型谷氨酸受体5(mGluR5)在甲基苯丙胺诱导的行为敏化中的作用。分别在不同实验中测试了mGluR5的正变构调节剂(3-氰基-N-(1,3-二苯基-1H-吡唑-5-基)苯甲酰胺(CDPPB)和负变构调节剂非诺班。将Sprague-Dawley大鼠反复注射1mg/kg甲基苯丙胺或生理盐水,然后使用0.5mg/kg甲基苯丙胺进行运动激发试验。在激发试验前,给大鼠注射CDPPB、非诺班或赋形剂。先前研究的剂量显示药物条件性行为减少;然而在本研究中,CDPPB和非诺班预处理均未导致行为敏化表达的改变,表明mGluR5不参与甲基苯丙胺诱导的敏化运动。此外,无论药物暴露史如何,高剂量(30mg/kg)的非诺班都会导致大鼠甲基苯丙胺诱导的运动减少,这表明存在非特异性行为抑制的证据。