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5-羟色胺3(5-HT3)受体拮抗剂昂丹司琼对美加明诱发的尼古丁戒断厌恶的减弱作用

Attenuation of mecamylamine-precipitated nicotine-withdrawal aversion by the 5-HT3 receptor antagonist ondansetron.

作者信息

Suzuki T, Ise Y, Mori T, Misawa M

机构信息

Department of Pharmacology, School of Pharmacy, Hoshi University, Tokyo, Japan.

出版信息

Life Sci. 1997;61(16):PL249-54. doi: 10.1016/s0024-3205(97)00745-5.

Abstract

The effect of ondansetron (0.01-0.1 mg/kg, s.c.), a selective 5-HT3 receptor antagonist, on mecamylamine-precipitated nicotine-withdrawal aversion was examined in the conditioned place preference paradigm. Male Sprague-Dawley rats were chronically treated subcutaneously with 9 mg/kg/day (-)-nicotine tartrate using an osmotic minipump. After nicotine treatment for 7 days, mecamylamine (1 mg/kg, s.c.), a nicotinic receptor antagonist, produced place aversion in nicotine-dependent rats. This aversive effect was dose-dependently antagonized by pretreatment with ondansetron 30 min prior to the conditioning. These results suggest that ondansetron may attenuate the place aversion associated with nicotine withdrawal, and may be useful for the treatment of nicotine dependence.

摘要

在条件性位置偏爱范式中,研究了选择性5-羟色胺3(5-HT3)受体拮抗剂昂丹司琼(0.01-0.1毫克/千克,皮下注射)对美加明诱发的尼古丁戒断厌恶反应的影响。雄性斯普拉格-道利大鼠用渗透微型泵皮下长期注射9毫克/千克/天的(-)-酒石酸尼古丁。尼古丁治疗7天后,烟碱受体拮抗剂美加明(1毫克/千克,皮下注射)在尼古丁依赖大鼠中产生位置厌恶。在条件反射前30分钟用昂丹司琼预处理可剂量依赖性地拮抗这种厌恶作用。这些结果表明,昂丹司琼可能减轻与尼古丁戒断相关的位置厌恶,可能对尼古丁依赖的治疗有用。

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