Perrine Shane A, Schroeder Joseph A, Unterwald Ellen M
Temple University School of Medicine, Department of Pharmacology and Center for Substance Abuse Research, 3420 N. Broad St., MRB 319, Philadelphia, PA 19140, United States.
Brain Res Mol Brain Res. 2005 Feb 18;133(2):224-32. doi: 10.1016/j.molbrainres.2004.10.025.
Behavioral sensitization is a characteristic sequelae of repeated cocaine exposure. It likely occurs due to long-lasting neuroadaptations produced by cocaine, although the exact nature of these adaptations has yet to be defined. The goal of the present study was to determine if behavioral sensitization to cocaine is accompanied by alterations in G-protein levels. Adult male rats were administered cocaine or saline three times daily in a binge-pattern for 1, 3, or 14 days and activity monitored. Levels of four major G-protein alpha-subunits, Galphas, Galphaolf, Galphao and Galphai1, and their mRNAs were measured in the nucleus accumbens, caudate putamen, and cingulate/frontal cortex using Western blot analysis and in situ hybridization, respectively. Fourteen days of binge-pattern cocaine administration resulted in behavioral sensitization as evidenced by increased behavioral activity over the 14 days of drug exposure. Results demonstrated that Galphaolf mRNA expression was significantly reduced in the nucleus accumbens after 1, 3 or 14 days of cocaine, whereas Galphai1 mRNA was increased following 3, but not 1 or 14 days of cocaine in the caudate putamen, nucleus accumbens and cingulate cortex. Galphas and Galphao mRNA expression were not altered in any region investigated at any time point. In contrast to gene expression, protein levels of the four G-protein alpha-subunits were not significantly different from saline-injected rats in the caudate putamen, nucleus accumbens, or frontal cortex following 1, 3, or 14 days of cocaine administration. These results suggest that alterations in the level of G-proteins are not necessary for the development of cocaine-induced sensitization.
行为敏化是反复接触可卡因后的一种典型后遗症。它可能是由于可卡因产生的持久神经适应性变化所致,尽管这些适应性变化的确切性质尚未明确。本研究的目的是确定对可卡因的行为敏化是否伴随着G蛋白水平的改变。成年雄性大鼠按暴饮模式每天接受三次可卡因或生理盐水注射,持续1、3或14天,并监测其活动情况。分别使用蛋白质印迹分析和原位杂交技术,在伏隔核、尾状壳核和扣带/额叶皮质中测量四种主要G蛋白α亚基(Gαs、Gαolf、Gαo和Gαi1)及其mRNA的水平。连续14天按暴饮模式给予可卡因导致行为敏化,表现为在14天的药物暴露期间行为活动增加。结果表明,在给予可卡因1、3或14天后,伏隔核中Gαolf mRNA表达显著降低,而在尾状壳核、伏隔核和扣带皮质中,给予可卡因3天后Gαi1 mRNA增加,而1天或14天后未增加。在任何时间点,所研究的任何区域中Gαs和Gαo mRNA表达均未改变。与基因表达相反,在给予可卡因1、3或14天后,尾状壳核、伏隔核或额叶皮质中四种G蛋白α亚基的蛋白质水平与注射生理盐水的大鼠相比无显著差异。这些结果表明,G蛋白水平的改变对于可卡因诱导的敏化发展并非必要。