Mantsch John R, Baker David A, Francis David M, Katz Eric S, Hoks Michael A, Serge Joseph P
Department of Biomedical Sciences, Marquette University, Schroeder Health Complex, P.O. Box 1881, Milwaukee, WI 53201-1881, USA.
Psychopharmacology (Berl). 2008 Jan;195(4):591-603. doi: 10.1007/s00213-007-0950-5. Epub 2007 Sep 26.
Stressful events during periods of drug abstinence likely contribute to relapse in cocaine-dependent individuals. Excessive cocaine use may increase susceptibility to stressor-induced relapse through alterations in brain corticotropin-releasing factor (CRF) responsiveness.
This study examined stressor- and CRF-induced cocaine seeking and other stress-related behaviors in rats with different histories of cocaine self-administration (SA).
Rats self-administered cocaine under short-access (ShA; 2 h daily) or long-access (LgA; 6 h daily) conditions for 14 days or were provided access to saline and were tested for reinstatement by a stressor (electric footshock), cocaine or an icv injection of CRF and for behavioral responsiveness on the elevated plus maze, in a novel environment and in the light-dark box after a 14- to 17-day extinction/withdrawal period.
LgA rats showed escalating patterns of cocaine SA and were more susceptible to reinstatement by cocaine, EFS, or icv CRF than ShA rats. Overall, cocaine SA increased activity in the center field of a novel environment, on the open arms of the elevated plus maze, and in the light compartment of a light-dark box. In most cases, the effects of cocaine SA were dependent on the pattern/amount of cocaine intake with statistically significant differences from saline self-administering controls only observed in LgA rats.
When examined after several weeks of extinction/withdrawal, cocaine SA promotes a more active pattern of behavior during times of stress that is associated with a heightened susceptibility to stressor-induced cocaine-seeking behavior and may be the consequence of augmented CRF regulation of addiction-related neurocircuitry.
在药物戒断期间的应激事件可能导致可卡因依赖个体复吸。过量使用可卡因可能通过改变大脑促肾上腺皮质激素释放因子(CRF)反应性增加对应激源诱导复吸的易感性。
本研究检测了不同可卡因自我给药(SA)史的大鼠中应激源和CRF诱导的可卡因觅求及其他应激相关行为。
大鼠在短时间给药(ShA;每日2小时)或长时间给药(LgA;每日6小时)条件下自我给药可卡因14天,或给予生理盐水,并在14至17天的消退/戒断期后,通过应激源(电足底电击)、可卡因或脑室内注射CRF测试复吸情况,以及在高架十字迷宫、新环境和明暗箱中测试行为反应性能力。
LgA大鼠表现出可卡因SA的递增模式,并且比ShA大鼠更容易因可卡因、电足底电击或脑室内注射CRF而复吸。总体而言,可卡因SA增加了在新环境中心区域、高架十字迷宫开放臂以及明暗箱亮区的活动。在大多数情况下,可卡因SA的影响取决于可卡因摄入量的模式/数量,仅在LgA大鼠中观察到与生理盐水自我给药对照组有统计学显著差异。
在数周的消退/戒断后进行检测时,可卡因SA在应激期间促进了更活跃的行为模式,这与对应激源诱导的可卡因觅求行为的易感性增加相关,并且可能是成瘾相关神经回路的CRF调节增强的结果。