Peng Xiao-Qing, Li Xia, Gilbert Jeremy G, Pak Arlene C, Ashby Charles R, Brodie Jonathan D, Dewey Stephen L, Gardner Eliot L, Xi Zheng-Xiong
Neuropsychopharmacology Section, Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, DHHS, Baltimore, MD 21224, United States.
Drug Alcohol Depend. 2008 Oct 1;97(3):216-25. doi: 10.1016/j.drugalcdep.2007.10.004. Epub 2007 Dec 11.
Relapse to drug use is a core feature of addiction. Previous studies demonstrate that gamma-vinyl GABA (GVG), an irreversible GABA transaminase inhibitor, attenuates the acute rewarding effects of cocaine and other addictive drugs. We here report that systemic administration of GVG (25-300 mg/kg) dose-dependently inhibits cocaine- or sucrose-induced reinstatement of reward-seeking behavior in rats. In vivo microdialysis data indicated that the same doses of GVG dose-dependently elevate extracellular GABA levels in the nucleus accumbens (NAc). However, GVG, when administered systemically or locally into the NAc, failed to inhibit either basal or cocaine-priming enhanced NAc dopamine in either naïve rats or cocaine extinction rats. These data suggest that: (1) GVG significantly inhibits cocaine- or sucrose-triggered reinstatement of reward-seeking behavior; and (2) a GABAergic-, but not dopaminergic-, dependent mechanism may underlie the antagonism by GVG of cocaine-triggered reinstatement of drug-seeking behavior, at least with respect to GVG's action on the NAc.
复吸是成瘾的一个核心特征。先前的研究表明,γ-乙烯基氨基丁酸(GVG),一种不可逆的γ-氨基丁酸转氨酶抑制剂,可减弱可卡因和其他成瘾药物的急性奖赏效应。我们在此报告,全身给予GVG(25 - 300毫克/千克)剂量依赖性地抑制大鼠中可卡因或蔗糖诱导的奖赏寻求行为的恢复。体内微透析数据表明,相同剂量的GVG剂量依赖性地提高伏隔核(NAc)细胞外γ-氨基丁酸水平。然而,当全身或局部给予NAc时,GVG未能抑制未接触过可卡因的大鼠或可卡因戒断大鼠的基础或可卡因启动增强的NAc多巴胺。这些数据表明:(1)GVG显著抑制可卡因或蔗糖触发的奖赏寻求行为的恢复;(2)至少就GVG对NAc的作用而言,一种γ-氨基丁酸能而非多巴胺能依赖的机制可能是GVG拮抗可卡因触发的觅药行为恢复的基础。