Alvarez-Jaimes Lily, Polis Ilham, Parsons Loren H
Committee on the Neurobiology of Addictive Disorders, The Scripps Research Institute, La Jolla, CA 92037, USA.
Open Neuropsychopharmacol J. 2009;2:77-85. doi: 10.2174/1876523800902020077.
Substantial evidence suggests a facilitatory influence of cannabinoid CB receptors in the modulation of ethanol consumption by rodents. Studies performed in rats selectively bred for high alcohol preference point to an involvement of CB receptors in the nucleus accumbens (NAC), ventral tegmental area (VTA) and medial prefrontal cortex (mPFC) in the modulation ethanol self-administration. However, the neural mechanisms through which CB receptors regulate ethanol intake in out-bred Wistar rats have not been investigated. The present study evaluated alterations in ethanol self-administration induced by localized infusions of the CB receptor antagonist SR141716A (0, 1 and 3 μg/side) into the NAC, anterior and posterior VTA and mPFC. Separate groups of Wistar rats were trained to operantly respond for an oral ethanol solution and prepared with bilateral injection cannulae aimed at each brain region. Results revealed significant decreases in ethanol intake following intra-NAC SR141716A administration, consistent with our prior observation of ethanol-induced increases extracellular 2-arachidonoyl glycerol (2-AG) in this brain region. We also observed a significant dose-dependent reduction in ethanol intake following SR141716A administration into the posterior, but not anterior VTA, consistent with evidence of a specific involvement of the posterior VTA in the regulation of ethanol intake. Ethanol consumption was unaltered following intra-mPFC SR141716A administration and ethanol self-administration did not induce robust changes in anandamide or 2-AG levels in mPFC microdialysates. These findings implicate an involvement of CB receptors in the NAC and posterior VTA, but not anterior VTA and mPFC in the regulation of ethanol self-administration behavior by outbred Wistar rats.
大量证据表明,大麻素CB受体对啮齿动物乙醇摄入量的调节具有促进作用。对选择性培育出的高酒精偏好大鼠进行的研究表明,伏隔核(NAC)、腹侧被盖区(VTA)和内侧前额叶皮质(mPFC)中的CB受体参与了乙醇自我给药的调节。然而,CB受体调节远交系Wistar大鼠乙醇摄入量的神经机制尚未得到研究。本研究评估了向NAC、VTA的前部和后部以及mPFC局部注射CB受体拮抗剂SR141716A(0、1和3μg/侧)所诱导的乙醇自我给药的变化。将不同组的Wistar大鼠训练为通过操作来获取口服乙醇溶液,并制备双侧注射套管,将其靶向每个脑区。结果显示,向NAC内注射SR141716A后,乙醇摄入量显著降低,这与我们之前观察到的该脑区中乙醇诱导的细胞外2-花生四烯酸甘油(2-AG)增加相一致。我们还观察到,向VTA后部而非前部注射SR141716A后,乙醇摄入量出现显著的剂量依赖性降低,这与后部VTA在乙醇摄入量调节中具有特定作用的证据相一致。向mPFC内注射SR141716A后,乙醇消耗量未发生改变,并且乙醇自我给药并未在mPFC微透析液中诱导花生四烯乙醇胺或2-AG水平发生显著变化。这些发现表明,NAC和VTA后部中的CB受体参与了远交系Wistar大鼠乙醇自我给药行为的调节,而VTA前部和mPFC中的CB受体则未参与。