Cheer J F, Kendall D A, Marsden C A
School of Biomedical Sciences, University of Nottingham Medical School, Queen's Medical Centre, UK.
Psychopharmacology (Berl). 2000 Jul;151(1):25-30. doi: 10.1007/s002130000481.
We wished to investigate further the hypothesis of an endogenous cannabinoid 'aversive counter-rewarding system, as the rewarding properties of cannabinoids using standard procedures remain ambiguous.
The purpose of this study was to confirm the behavioural effects of a highly potent synthetic cannabinoid agonist (HU210) and the selective cannabinoid antagonist SR 141716A using conditioned place preference (CPP).
HU210 (20, 60 and 100 microg kg(-1), SR141716A (0.25, 0.5, 2 and 3 mg kg(-1)), cocaine (15 mg kg(-1) and delta9-THC (1.5 mg kg(-1)) were given to male Lister hooded rats using an unbiased CPP design.
SR141716A and cocaine produced place preference at all doses tested, whereas HU210 and delta9-THC produced aversion as expressed by time spent in the drug-paired compartment of the CPP apparatus.
The aversive effects of cannabinoid agonists and the rewarding effect of the cannabinoid antagonist are suggestive of a cannabinergic tone in the rat brain. Further research is needed to determine the precise relationship of that tone with the reward pathways of the brain.
由于使用标准程序时大麻素的奖赏特性仍不明确,我们希望进一步研究内源性大麻素“厌恶反奖赏系统”的假说。
本研究的目的是使用条件性位置偏爱(CPP)来确认一种高效合成大麻素激动剂(HU210)和选择性大麻素拮抗剂SR 141716A的行为效应。
采用无偏倚的CPP设计,将HU210(20、60和100微克/千克)、SR141716A(0.25、0.5、2和3毫克/千克)、可卡因(15毫克/千克)和δ9-四氢大麻酚(1.5毫克/千克)给予雄性利斯特戴帽大鼠。
SR141716A和可卡因在所有测试剂量下均产生位置偏爱,而HU210和δ9-四氢大麻酚则产生厌恶,表现为在CPP装置的药物配对隔室中停留的时间。
大麻素激动剂的厌恶效应和大麻素拮抗剂的奖赏效应提示大鼠大脑中存在大麻素能张力。需要进一步研究以确定该张力与大脑奖赏通路的确切关系。