Department of Psychiatry and Neuroscience Graduate Program, The Seay Center for Basic and Applied Research in Psychiatric Illness, UT Southwestern Medical Center, Dallas, TX 75390-9070, USA.
Addict Biol. 2011 Jul;16(3):450-7. doi: 10.1111/j.1369-1600.2010.00296.x. Epub 2011 Feb 11.
Reexposure to cocaine-associated environments promotes relapse to cocaine seeking and represents a persistent impediment to successful abstinence. Neurobiological adaptations are thought to underlie the preservation of drug-seeking behavior during protracted withdrawal periods, possibly including changes associated specifically with cocaine-paired contexts. We measured GluR(1) (S845) and extracellular signal-regulated kinase (ERK) phosphorylation in rat striatal subregions in an animal model of cocaine relapse. Animals with cocaine self-administration experience and their yoked partners were exposed to extinction conditions for one hour in the drug-paired environmental context after one day or three weeks withdrawal to measure protein phosphorylation induced by the cocaine-paired context in the absence of cocaine reinforcement. GluR(1) (S845) (an index of protein kinase A (PKA) activity) and ERK phosphorylation increased in the nucleus accumbens core of self-administering but not yoked animals after three weeks (but not one day) withdrawal, indicating a time-dependent emergence of context-associated protein phosphorylation in this accumbens subregion. In comparison, animals trained to self-administer sucrose displayed a similar increase in ERK, but not GluR(1) (S845) , phosphorylation following reexposure to a sucrose-paired environment three weeks later, indicating that GluR(1) (S845) phosphorylation did not result solely from lever press behavior per se. In contrast, basal (home cage) GluR(1) (S845) phosphorylation was elevated in the nucleus accumbens shell and caudate-putamen after one day or three weeks cocaine withdrawal regardless of context exposure. These results suggest that time-dependent emergence of context-associated GluR(1) (S845) phosphorylation in the nucleus accumbens core may contribute to the persistence of cocaine-seeking behavior, whereas ERK phosphorylation may be a consequence of this behavior.
重新暴露于可卡因相关环境中会促进可卡因觅药行为的复发,是成功戒除可卡因的持续障碍。神经生物学适应被认为是在长期戒断期间保留觅药行为的基础,可能包括与可卡因配对环境相关的特定变化。我们在可卡因复吸动物模型中测量了大鼠纹状体亚区的 GluR(1) (S845) 和细胞外信号调节激酶 (ERK) 磷酸化。在一天或三周戒断后,有可卡因自我给药经验的动物及其配对的同伴在可卡因配对环境中暴露于消退条件下一小时,以测量在没有可卡因强化的情况下,可卡因配对环境诱导的蛋白磷酸化。GluR(1) (S845) (蛋白激酶 A (PKA) 活性的指标) 和 ERK 磷酸化在自我给药但不是配对动物的伏隔核核心中增加,这表明在该伏隔核亚区中,与环境相关的蛋白磷酸化随着时间的推移而出现。相比之下,经过训练自我给予蔗糖的动物在三周后重新暴露于蔗糖配对环境时,ERK 而不是 GluR(1) (S845) 磷酸化增加,表明 GluR(1) (S845) 磷酸化不仅仅是由于杠杆按压行为本身。相比之下,无论环境暴露如何,在一天或三周可卡因戒断后,伏隔核壳和尾壳核中的基础 (笼内) GluR(1) (S845) 磷酸化升高。这些结果表明,伏隔核核心中与环境相关的 GluR(1) (S845) 磷酸化的时间依赖性出现可能有助于可卡因觅药行为的持续存在,而 ERK 磷酸化可能是这种行为的结果。