Grant K A, Barrett J E
Unit for Special Projects, National Institute on Alcohol Abuse and Alcoholism, Rockville, MD 20852.
Psychopharmacology (Berl). 1991;104(4):451-6. doi: 10.1007/BF02245648.
The ability of selective 5-HT3 receptor antagonists to block the discriminative stimulus effects of ethanol was investigated in pigeons trained with food reinforcement to discriminate ethanol (1.5 g/kg; IG) from water. The 5-HT3 receptor antagonists that are substituted tropines, ICS 205-930 (0.1-0.56 mg/kg) and MDL 72222 (3.0-17.0 mg/kg), blocked ethanol-appropriate responding, in a dose-dependent manner, suggesting that some of the discriminative stimulus effects of ethanol are mediated via the 5-HT3 receptor. The blockade the discriminative stimulus effects of ethanol occurred in the presence of approximately 25-40 mM blood ethanol levels. Furthermore, the ethanol dose-effect function was shifted to the right by increasing doses of MDL 72222, suggesting a surmountable antagonism of the discriminative stimulus effects of ethanol. However, the benzamide zacopride (0.56-1.7 mg/kg), which is also a 5-HT3 receptor antagonist, did not block the discriminative stimulus effects of ethanol. In addition, the dopaminergic antagonist haloperidol and the 5-HT2 receptor antagonist ketanserin also failed to block the ethanol discrimination. The results suggest that 5-HT3 mediated neurotransmission is an important component of ethanol's discriminative stimulus effects, but that the structural characteristics of the selective 5-HT3 receptor antagonists influence their ability to block this action of ethanol.(ABSTRACT TRUNCATED AT 250 WORDS)
在以食物强化训练来区分乙醇(1.5克/千克;灌胃)和水的鸽子中,研究了选择性5-羟色胺3(5-HT3)受体拮抗剂阻断乙醇辨别刺激效应的能力。作为取代托品的5-HT3受体拮抗剂,ICS 205-930(0.1 - 0.56毫克/千克)和MDL 72222(3.0 - 17.0毫克/千克)以剂量依赖性方式阻断了与乙醇相符的反应,这表明乙醇的一些辨别刺激效应是通过5-HT3受体介导的。乙醇辨别刺激效应的阻断发生在血液乙醇水平约为25 - 40毫摩尔时。此外,随着MDL 72222剂量增加,乙醇剂量 - 效应函数向右移动,表明对乙醇辨别刺激效应存在可克服的拮抗作用。然而,同样作为5-HT3受体拮抗剂的苯甲酰胺类药物扎考必利(0.56 - 1.7毫克/千克)并未阻断乙醇的辨别刺激效应。此外,多巴胺能拮抗剂氟哌啶醇和5-HT2受体拮抗剂酮色林也未能阻断乙醇辨别。结果表明,5-HT3介导的神经传递是乙醇辨别刺激效应的重要组成部分,但选择性5-HT3受体拮抗剂的结构特征会影响其阻断乙醇这一作用的能力。(摘要截短于250字)