Valzachi Maria Cristina, Teodorov Elizabeth, Marcourakis Tania, Bailey Alexis, Camarini Rosana
Departamento de Farmacologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, SP, Brazil.
PLoS One. 2013 Oct 21;8(10):e78317. doi: 10.1371/journal.pone.0078317. eCollection 2013.
Adolescence has been linked to greater risk-taking and novelty-seeking behavior and a higher prevalence of drug abuse and risk of relapse. Decreases in cyclic adenosine monophosphate response element binding protein (CREB) and phosphorylated CREB (pCREB) have been reported after repeated cocaine administration in animal models. We compared the behavioral effects of cocaine and abstinence in adolescent and adult mice and investigated possible age-related differences in CREB and pCREB levels. Adolescent and adult male Swiss mice received one daily injection of saline or cocaine (10 mg/kg, i.p.) for 8 days. On day 9, the mice received a saline injection to evaluate possible environmental conditioning. After 9 days of withdrawal, the mice were tested in the elevated plus maze to evaluate anxiety-like behavior. Twelve days after the last saline/cocaine injection, the mice received a challenge injection of either cocaine or saline, and locomotor activity was assessed. One hour after the last injection, the brains were extracted, and CREB and pCREB levels were evaluated using Western blot in the prefrontal cortex (PFC) and hippocampus. The cocaine-pretreated mice during adolescence exhibited a greater magnitude of the expression of behavioral sensitization and greater cocaine withdrawal-induced anxiety-like behavior compared with the control group. Significant increases in CREB levels in the PFC and hippocampus and pCREB in the hippocampus were observed in cocaine-abstinent animals compared with the animals treated with cocaine in adulthood. Interestingly, significant negative correlations were observed between cocaine sensitization and CREB levels in both regions. These results suggest that the behavioral and neurochemical consequences of psychoactive substances in a still-developing nervous system can be more severe than in an already mature nervous system.
青春期与更高的冒险和寻求新奇行为以及更高的药物滥用患病率和复发风险有关。在动物模型中,反复给予可卡因后,已报道环磷酸腺苷反应元件结合蛋白(CREB)和磷酸化CREB(pCREB)水平降低。我们比较了可卡因和禁欲对青春期和成年小鼠的行为影响,并研究了CREB和pCREB水平可能存在的年龄相关差异。青春期和成年雄性瑞士小鼠每天腹腔注射一次生理盐水或可卡因(10mg/kg),持续8天。在第9天,给小鼠注射生理盐水以评估可能的环境条件作用。戒断9天后,在高架十字迷宫中测试小鼠以评估焦虑样行为。在最后一次注射生理盐水/可卡因12天后,给小鼠注射一次可卡因或生理盐水进行激发注射,并评估其运动活性。最后一次注射1小时后,取出大脑,使用蛋白质免疫印迹法评估前额叶皮质(PFC)和海马体中CREB和pCREB的水平。与对照组相比,青春期接受可卡因预处理的小鼠表现出更大程度的行为敏化表达和更大的可卡因戒断诱导的焦虑样行为。与成年期接受可卡因治疗的动物相比,在可卡因戒断的动物中观察到PFC和海马体中CREB水平以及海马体中pCREB水平显著增加。有趣的是,在这两个区域中,可卡因敏化与CREB水平之间均观察到显著的负相关。这些结果表明,精神活性物质在仍在发育的神经系统中产生的行为和神经化学后果可能比在已经成熟的神经系统中更为严重。