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Wiley InterScience

Addiction Biology

Addiction Biology

Volume 12 Issue 3-4, Pages 470 - 477

Published Online: 30 Apr 2007

Journal compilation © 2010 Society for the Study of Addiction



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ORIGINAL INVESTIGATIONS ON CPP
Development, extinction and reinstatement of morphine withdrawal-induced conditioned place aversion in rats
Yi Li*, Xuebing Liu*, Hongxian Chen, Huiqiong Deng, Xiaojun Xiang, Hanhui Chen & Wei Hao
Mental Health Institute and WHO Collaborating Center for Psychosocial Factors, Drug Abuse and Health, the 2nd Xiangya Hospital, Central South University, China
Correspondence to  Wei Hao, Professor of Psychiatry, Mental Health Institute and WHO Collaborating Center for Psychosocial Factors, Drug Abuse and Health, the 2nd Xiangya Hospital, Central South University, Changsha 410011, Hunan, China. E-mail: weihao57@china.com

  *Now working at Mental Hospital of Tongji Medical College (Wuhan Mental Health Center), Huazhong University Science & Technology, Wuhan 430022, China.

Copyright © 2007 The Authors. Journal compilation © 2007 Society for the Study of Addiction
KEYWORDS
Conditioned place aversion • extinction • morphine • negative reinforcement • reinstatement • withdrawal

ABSTRACT

AbstractINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONAcknowledgementsReferences

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.


DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1369-1600.2007.00059.x About DOI

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