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大鼠吗啡戒断诱导的条件性位置厌恶的形成、消退和恢复

Development, extinction and reinstatement of morphine withdrawal-induced conditioned place aversion in rats.

作者信息

Li Yi, Liu Xuebing, Chen Hongxian, Deng Huiqiong, Xiang Xiaojun, Chen Hanhui, Hao Wei

机构信息

Mental Health Institute and WHO Collaborating Center for Psychosocial Factors, Drug Abuse and Health, the 2nd Xiangya Hospital, Central South University, China.

出版信息

Addict Biol. 2007 Sep;12(3-4):470-7. doi: 10.1111/j.1369-1600.2007.00059.x.

Abstract

The motivational component of drug withdrawal may contribute to drug seeking and relapse through the negative reinforcement-based process. Here, we used conditioned place aversion (CPA) induced by naloxone-precipitated morphine withdrawal to measure the aversive effects. Using an unbiased conditioning paradigm, we treated rats with morphine hydrochloride [(10 mg/kg intraperitoneally (i.p.)] twice per day (at 08:00 and 20:00) for 6.5 days (from day 1 to day 7 morning), while gave them naloxone (0.3 mg/kg i.p.) on day 6, a precipitated withdrawal paired with a compartment that caused CPA to the side. Then, the rats exhibited CPA were received 12 extinction trials from days 7 to 13, by daily exposed to the two compartments for free exploration. On day 13, the rats with extinguished CPA were treated with a priming injection of morphine (10 mg/kg i.p.) followed by naloxone (0.3 mg/kg i.p.) that reliably reinstated CPA. These results demonstrated that repeatedly morphine-treated rats showed the formation, extinction and reinstatement of CPA. The present CPA model induced by these procedures may be useful for studying the biological mechanisms underlying the aversive motivational component of opiate withdrawal.

摘要

药物戒断的动机成分可能通过基于负强化的过程导致觅药行为和复吸。在此,我们使用纳洛酮诱发的吗啡戒断所诱导的条件性位置厌恶(CPA)来测量厌恶效应。采用无偏倚的条件化范式,我们每天两次(上午8点和晚上8点)给大鼠腹腔注射盐酸吗啡[(10毫克/千克)],持续6.5天(从第1天至第7天上午),而在第6天给它们腹腔注射纳洛酮(0.3毫克/千克),这一戒断诱发过程与一个导致对该侧产生CPA的隔室配对。然后,对表现出CPA的大鼠在第7天至第13天进行12次消退试验,每天让它们自由探索这两个隔室。在第13天,对已消退CPA的大鼠先腹腔注射一次吗啡(10毫克/千克)进行激发,随后腹腔注射纳洛酮(0.3毫克/千克),这可靠地恢复了CPA。这些结果表明,反复用吗啡处理的大鼠表现出CPA的形成、消退和恢复。通过这些程序诱导的当前CPA模型可能有助于研究阿片类药物戒断厌恶动机成分背后的生物学机制。

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