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刺激内侧前额叶皮质的 5-羟色胺 2C(5-HT(2C))受体可减弱可卡因觅药行为。

Stimulation of medial prefrontal cortex serotonin 2C (5-HT(2C)) receptors attenuates cocaine-seeking behavior.

机构信息

Department of Psychology, Arizona State University, Tempe, 85287-1104, USA.

出版信息

Neuropsychopharmacology. 2010 Sep;35(10):2037-48. doi: 10.1038/npp.2010.72. Epub 2010 Jun 2.

Abstract

Serotonin 2C receptor (5-HT(2C)R) agonists administered systemically attenuate both cocaine-primed and cue-elicited reinstatement of extinguished cocaine-seeking behavior. To further elucidate the function of these receptors in addiction-like processes, this study examined the effects of microinfusing the 5-HT(2C)R agonist MK212 (0, 10, 30, 100 ng/side/0.2 microl) into the medial prefrontal cortex (mPFC) on cocaine self-administration and reinstatement of extinguished cocaine-seeking behavior. Male Sprague-Dawley rats were trained to self-administer cocaine (0.75 mg/kg, i.v.) paired with light and tone cues. Once responding stabilized, rats received MK212 microinfusions before tests for maintenance of cocaine self-administration. Next, extinction training to reduce cocaine-seeking behavior, defined as responses performed without cocaine reinforcement available, occurred until low extinction baselines were achieved. Rats then received MK212 microinfusions before tests for reinstatement of extinguished cocaine-seeking behavior elicited by cocaine-priming injections (10 mg/kg, i.p.) or response-contingent presentations of the cocaine-associated cues; operant responses during cocaine-primed reinstatement tests produced no consequences. MK212 microinfusions into the prelimbic and infralimbic, but not anterior cingulate, regions of the mPFC dose-dependently attenuated both cocaine-primed and cue-elicited reinstatement of extinguished cocaine-seeking behavior, but did not reliably affect cocaine self-administration. A subsequent experiment showed that the effects of MK212 (100 ng/side/0.2 microl) on reinstatement of extinguished cocaine-seeking behavior were blocked by co-administration of the 5-HT(2C)R antagonist SB242084 (200 ng/side/0.2 microl). MK212 administered alone into the mPFC as a drug prime produced no discernable effects on cocaine-seeking behavior. These findings suggest that stimulation of 5-HT(2C)Rs in the mPFC attenuates the incentive motivational effects produced by sampling cocaine or exposure to drug-paired cues.

摘要

5-羟色胺 2C 受体(5-HT2CR)激动剂全身给药可减弱可卡因引发和线索诱发的已消退可卡因寻求行为的复燃。为了进一步阐明这些受体在成瘾样过程中的作用,本研究检查了将 5-HT2CR 激动剂 MK212(0、10、30、100ng/侧/0.2μl)微注入内侧前额叶皮层(mPFC)对可卡因自我给药和已消退可卡因寻求行为复燃的影响。雄性 Sprague-Dawley 大鼠接受训练以静脉内给予可卡因(0.75mg/kg)与光和音调线索配对自我给药。一旦反应稳定,在测试维持可卡因自我给药之前,大鼠接受 MK212 微注射。接下来,进行消退训练以减少可卡因寻求行为,定义为在没有可卡因强化的情况下进行的反应,直到达到低消退基线。然后,在可卡因引发的可卡因寻求行为复燃测试(10mg/kg,ip)或与可卡因相关线索的操作性反应引发的复燃测试之前,给予大鼠 MK212 微注射;可卡因引发的复燃测试中的操作反应没有产生后果。MK212 微注入 mPFC 的额前叶和下边缘区域,但不是前扣带皮层,剂量依赖性地减弱了可卡因引发和线索诱发的已消退可卡因寻求行为的复燃,但对可卡因自我给药没有可靠影响。随后的实验表明,MK212(100ng/侧/0.2μl)对已消退可卡因寻求行为复燃的作用被 5-HT2CR 拮抗剂 SB242084(200ng/侧/0.2μl)共同给药阻断。单独在 mPFC 中给予 MK212 作为药物引发对可卡因寻求行为没有产生明显影响。这些发现表明,mPFC 中 5-HT2CR 的刺激减弱了可卡因采样或暴露于药物配对线索产生的激励动机效应。

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