Feltenstein Matthew W, Byrd Elizabeth A, Henderson Alisha R, See Ronald E
Department of Neurosciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Psychoneuroendocrinology. 2009 Apr;34(3):343-52. doi: 10.1016/j.psyneuen.2008.09.014. Epub 2008 Nov 1.
Clinical research suggests that gender differences exist in cocaine dependence. Similarly, preclinical studies have shown that female rats exhibit higher response rates during cocaine self-administration, early extinction, and cocaine-primed reinstatement of drug-seeking. These effects are also estrous cycle dependent and inversely related to plasma progesterone, in that proestrus females (high progesterone) exhibit less cocaine-seeking, while estrous females (low progesterone) show the greatest cocaine-seeking. Based on these findings, we hypothesized that progesterone would attenuate cocaine-seeking behavior in intact, freely cycling animals. The role of the estrous cycle on cocaine-seeking behavior during early (first acquisition day) versus late (last maintenance day) cocaine self-administration was also examined. Female, Sprague-Dawley rats self-administered cocaine (0.5 mg/kg/infusion, IV) along a FR1 schedule, followed by daily extinction sessions in the absence of cocaine reinforcement. Once responding was extinguished, rats received an injection of cocaine (10 mg/kg, IP) immediately prior to reinstatement testing. Progesterone (2 mg/kg, SC) or vehicle was administered 20 and 2h prior to the first day of extinction (early cocaine withdrawal) and the reinstatement trials. To determine estrous cycle phase, we assessed vaginal cytology prior to the first acquisition and last maintenance days of cocaine self-administration, the first day of extinction training, and each reinstatement test. During early and late cocaine self-administration, proestrus and estrous females exhibited the greatest levels of active lever responding, respectively. A significant increase in responding also occurred during cocaine-primed reinstatement for estrous versus nonestrous females, an effect that was selectively attenuated by progesterone. However, progesterone was not effective at reducing cocaine-primed reinstatement for females in other phases of the estrous cycle, nor was it effective at reducing cocaine-seeking during early withdrawal. Taken together, these results suggest that progesterone may be a useful therapeutic for preventing relapse in abstinent female cocaine users, especially when the likelihood of relapse is greatest.
临床研究表明,可卡因成瘾存在性别差异。同样,临床前研究显示,雌性大鼠在可卡因自我给药、早期消退以及可卡因引发的觅药行为恢复过程中表现出更高的反应率。这些效应也依赖于发情周期,且与血浆孕酮呈负相关,即发情前期的雌性大鼠(孕酮水平高)表现出较少的觅可卡因行为,而发情期的雌性大鼠(孕酮水平低)表现出最强的觅可卡因行为。基于这些发现,我们推测孕酮会减弱完整的、自由循环的动物的觅可卡因行为。我们还研究了发情周期在早期(首次获取日)与晚期(最后维持日)可卡因自我给药期间对觅可卡因行为的作用。雌性Sprague-Dawley大鼠按照FR1程序自我给药可卡因(0.5毫克/千克/输注,静脉注射),随后在没有可卡因强化的情况下进行每日消退训练。一旦反应消退,大鼠在恢复测试前立即注射可卡因(10毫克/千克,腹腔注射)。在消退训练的第一天(早期可卡因戒断)和恢复试验前20小时和2小时,给予孕酮(2毫克/千克,皮下注射)或赋形剂。为了确定发情周期阶段,我们在可卡因自我给药的首次获取日和最后维持日、消退训练的第一天以及每次恢复测试前评估阴道细胞学。在早期和晚期可卡因自我给药期间,发情前期和发情期的雌性大鼠分别表现出最高水平的主动杠杆反应。在可卡因引发的恢复过程中,发情期雌性大鼠与非发情期雌性大鼠相比,反应也显著增加,孕酮可选择性地减弱这种效应。然而,孕酮对处于发情周期其他阶段的雌性大鼠减少可卡因引发的恢复无效,对早期戒断期间减少觅可卡因行为也无效。综上所述,这些结果表明,孕酮可能是预防戒断的女性可卡因使用者复发的一种有用疗法,尤其是在复发可能性最大的时候。