Mantsch John R, Baker David A, Serge Joseph P, Hoks Michael A, Francis David M, Katz Eric S
Department of Biomedical Sciences, Marquette University, Milwaukee, WI 53201, USA.
Neuropsychopharmacology. 2008 Mar;33(4):814-26. doi: 10.1038/sj.npp.1301464. Epub 2007 May 30.
The loss of control over cocaine use and persistently heightened susceptibility to drug relapse that define human cocaine addiction are consequences of drug-induced neuroplasticity and can be studied in rats self-administering cocaine under conditions of daily long access (LgA) as escalating patterns of drug intake and heightened susceptibility to reinstatement. This study investigated the potential contribution of elevated glucocorticoids at the time of LgA cocaine self-administration (SA) to these behavioral indices of addiction-related neuroplasticity. Rats provided 14 days of 6-h access (LgA) to cocaine showed a progressive escalation of SA and were more susceptible to cocaine-induced reinstatement (10 mg/kg, i.p.) compared to rats self-administering under short-access (ShA; 2 h) conditions. A surgical adrenalectomy and corticosterone replacement (ADX/C) regimen that eliminated SA-induced increases in corticosterone (CORT) while maintaining the diurnal pattern of secretion failed to alter SA or reinstatement in ShA rats but slowed escalation and attenuated later reinstatement in LgA rats when applied before but not after chronic LgA SA testing. Although the contribution of other adrenal hormones cannot be ruled out, these data suggest that elevated glucocorticoids at the time of cocaine exposure may be required for the effects of LgA SA on cocaine intake and later reinstatement. The inability of daily CORT administration before daily ShA SA, at a dose that reproduced the response during LgA SA, to mimic the effects of LgA SA suggests that elevated glucocorticoids during SA may play a permissive role in cocaine-induced neuroplasticity that contributes to addiction.
对可卡因使用失去控制以及对药物复吸的持续高度易感性,这些定义人类可卡因成瘾的特征是药物诱导的神经可塑性的结果,并且可以在大鼠每日长时间获取(LgA)可卡因自我给药的条件下进行研究,作为药物摄入的升级模式和对复吸的高度易感性。本研究调查了在LgA可卡因自我给药(SA)时糖皮质激素升高对这些成瘾相关神经可塑性行为指标的潜在贡献。与在短时间获取(ShA;2小时)条件下自我给药的大鼠相比,给予14天每天6小时获取(LgA)可卡因的大鼠显示出SA的逐渐升级,并且对可卡因诱导的复吸(10mg/kg,腹腔注射)更易感。一种手术去肾上腺和皮质酮替代(ADX/C)方案,消除了SA诱导的皮质酮(CORT)增加,同时维持昼夜分泌模式,未能改变ShA大鼠的SA或复吸,但在慢性LgA SA测试之前而非之后应用时,减缓了LgA大鼠的升级并减弱了后期复吸。尽管不能排除其他肾上腺激素的作用,但这些数据表明,可卡因暴露时糖皮质激素升高可能是LgA SA对可卡因摄入和后期复吸产生影响所必需的。在每日ShA SA之前每日给予CORT,剂量能够重现LgA SA期间的反应,但无法模拟LgA SA的效果,这表明SA期间糖皮质激素升高可能在可卡因诱导的神经可塑性中起允许作用,这种神经可塑性导致成瘾。