Wong Wai Chong, Marinelli Michela
Department of Cellular and Molecular Pharmacology, Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Department of Dermatology, Brown University, Providence, RI, USA.
Addict Biol. 2016 May;21(3):634-45. doi: 10.1111/adb.12284. Epub 2015 Jul 23.
Adolescent rats take cocaine more readily than adults, are more sensitive to lower doses of the drug and work harder for it. It remains unknown if adolescent-onset of cocaine use has long-term consequences on adult relapse liability. Therefore, we tested if self-administering cocaine during adolescence impacts subsequent stress-induced reinstatement to cocaine seeking and taking, after a prolonged drug-free period. Adolescent (P42) or adult (P88) rats self-administered cocaine (0.6 or 1.2 mg/kg/infusion) for 7 or 10 days. Then, they underwent a prolonged drug-free period (21-40 days), after which they were tested for reinstatement of cocaine-seeking (i.e. responding in the absence of cocaine) induced by the stress hormone corticosterone, the pharmacological stressor yohimbine or electric footshock. Studies employed either single extinction session (within-session extinction/reinstatement) or repeated extinction prior to reinstatement (between-session extinction/reinstatement). Finally, in a separate set of experiments, rats underwent a prolonged drug-free period (40 days) and were then allowed to self-administer cocaine again, using progressive-ratio procedures that appraise the reinforcing efficacy of cocaine. Rats with adolescent-onset of cocaine use showed greater stress-induced reinstatement of cocaine seeking than rats with adult-onset of cocaine use. This was observed across conditions, providing external validity to these results. Groups did not differ on drug taking in progressive-ratio tests. Our studies indicate that experiencing cocaine during adolescence renders subjects particularly responsive to the subsequent effects of stress on drug seeking. This heightened propensity for reinstatement puts adolescent-onset drug users at heightened risk for relapse.
青春期大鼠比成年大鼠更容易摄取可卡因,对较低剂量的该药物更敏感,且为获取可卡因会付出更多努力。目前尚不清楚青春期开始使用可卡因是否会对成年后的复吸倾向产生长期影响。因此,我们测试了青春期期间自行服用可卡因是否会在一段较长的戒毒期后,影响随后应激诱导的对可卡因寻求和摄取行为的恢复。青春期(约42日龄)或成年(88日龄)大鼠自行服用可卡因(0.6或1.2毫克/千克/注射)7或10天。然后,它们经历一段较长的戒毒期(21 - 40天),之后测试应激激素皮质酮、药理应激剂育亨宾或电击足底诱发的可卡因寻求行为恢复情况(即在无可卡因情况下的反应)。研究采用单次消退试验(试验内消退/恢复)或恢复前的重复消退(试验间消退/恢复)。最后,在另一组实验中,大鼠经历一段较长的戒毒期(约40天),然后使用评估可卡因强化效力的累进比率程序,让它们再次自行服用可卡因。青春期开始使用可卡因的大鼠比成年期开始使用可卡因的大鼠表现出更强的应激诱导的可卡因寻求行为恢复。在各种条件下均观察到这一现象,为这些结果提供了外部有效性。在累进比率测试中,各组在药物摄取方面没有差异。我们的研究表明,青春期接触可卡因会使个体对随后应激对药物寻求行为的影响特别敏感。这种增强的恢复倾向使青春期开始使用毒品的人复吸风险增加。