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急性和亚慢性尼古丁预处理对吗啡状态依赖性学习的影响。

Influence of acute and sub-chronic nicotine pretreatment on morphine state-dependent learning.

作者信息

Zarrindast Mohammad-Reza, Nouraei Negin, Khallilzadeh Azita, Askari Elham

机构信息

Department of Pharmacology and Iranian National Center for Addiction Studies, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Behav Brain Res. 2006 Oct 16;173(2):268-73. doi: 10.1016/j.bbr.2006.06.032. Epub 2006 Aug 8.

Abstract

In the present study, the effects of acute and sub-chronic pretreatment of nicotine on impairment of memory formation and the state-dependent learning by morphine have been investigated in mice. Pre-training administration of morphine (5mg/kg) decreased the learning of a one-trial passive avoidance task, which was reversed by pre-test administration of the same dose of morphine. Amnesia induced by pre-training morphine was also significantly reversed in nicotine (0.001, 0.01 and 0.1 mg/kg)-treated animals on the test day. Morphine induced amnesia was also reversed in animals which had previously received sub-chronic injections of nicotine, once daily for 3 days followed by 14 days of no drug treatment. The restoration of memory by pre-test morphine was also reduced in animals which had previously received once daily injections of atropine (0.25, 0.5 and 1 mg/kg, i.p.) for 3 days after 14 of being days drug free. In the animals, restoration of memory by sub-chronic nicotine administration, was also decreased by once daily administration of atropine (0.25, 0.5 and 1 mg/kg) 10 min prior to injection of nicotine (0.1 microg/kg/day, for 3 days) but not with SCH 23390; R(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine HCl (0.01, 0.05 and 0.1 mg/kg) or sulpiride (25, 50 and 100 mg/kg) during 3-days of treatment with nicotine. The results suggest that nicotine may induce sensitization which affects the impairment of memory formation via cholinergic but not dopaminergic systems.

摘要

在本研究中,已对小鼠中尼古丁急性和亚慢性预处理对吗啡所致记忆形成损害及状态依赖性学习的影响进行了研究。预训练给予吗啡(5mg/kg)会降低单次被动回避任务的学习能力,而在预测试给予相同剂量的吗啡时这种情况会逆转。在测试当天,经尼古丁(0.001、0.01和0.1mg/kg)处理的动物中,预训练吗啡诱导的失忆也得到了显著逆转。吗啡诱导的失忆在先前接受过尼古丁亚慢性注射(每天一次,共3天,随后14天不进行药物治疗)的动物中也得到了逆转。在停药14天后,先前每天注射阿托品(0.25、0.5和1mg/kg,腹腔注射)3天的动物中,预测试吗啡对记忆的恢复作用也降低了。在这些动物中,亚慢性给予尼古丁对记忆的恢复作用,在注射尼古丁(0.1μg/kg/天,共3天)前10分钟每天给予阿托品(0.25、0.5和1mg/kg)时也降低了,但在给予SCH 23390;R(+)-7-氯-8-羟基-3-甲基-1-苯基-2,3,4,5-四氢-1H-3-苯并氮杂卓盐酸盐(0.01、0.05和0.1mg/kg)或舒必利(25、50和100mg/kg)并持续用尼古丁治疗3天时则未降低。结果表明,尼古丁可能诱导致敏作用,其通过胆碱能而非多巴胺能系统影响记忆形成的损害。

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