Kodas E, Cohen C, Louis C, Griebel G
Department of Psychopharmacology, Sanofi-Aventis Research and Development, 31 avenue Paul Vaillant-Couturier, 92220, Bagneux, France.
Psychopharmacology (Berl). 2007 Oct;194(2):161-71. doi: 10.1007/s00213-007-0813-0. Epub 2007 Jun 8.
The endocannabinoid system plays an important role in conditioned drug seeking, but the neuronal mechanisms involved in this behavior are unclear.
Here, we evaluate the role of endogenous cannabinoids in the cortico-limbic circuitry in cue-induced nicotine-seeking behavior in rats.
Animals were first trained to self-administer nicotine (0.03 mg/kg/injection, IV) under conditions in which responding was reinforced jointly by response-contingent nicotine injections and audiovisual stimuli. During subsequent sessions, nicotine was withdrawn and responding was reinforced by contingent presentation of the stimuli only. One month after nicotine removal, the cannabinoid CB1 receptor antagonist, rimonabant, was injected bilaterally into the shell of the nucleus accumbens (ShNAcc, 0.3, 3, or 30 ng/0.5 microl), the basolateral amygdala (BLA, 30 ng/0.5 microl), or the prelimbic cortex (PLCx, 30 ng/0.5 microl).
Rimonabant injected into the ShNAcc dose-dependently reduced nicotine-seeking behavior without modifying spontaneous locomotor activity. Similar results were obtained when the drug (30 ng) was injected into the BLA or the PLCx. The anatomical specificity was confirmed in a control experiment using [(3)H]rimonabant. Fifteen minutes after drug injection, when the behavioral effects of rimonabant were already achieved, radioactivity was detected at the site of injection and had not diffused to adjacent regions.
These findings demonstrate that increased endocannabinoid transmission critically triggers conditioned nicotine-seeking behavior in key cortico-limbic regions.
内源性大麻素系统在条件性药物寻求行为中起重要作用,但参与该行为的神经机制尚不清楚。
在此,我们评估内源性大麻素在大鼠线索诱导的尼古丁寻求行为的皮质-边缘回路中的作用。
首先训练动物在响应依赖性尼古丁注射和视听刺激共同强化响应的条件下自我注射尼古丁(0.03mg/kg/注射,静脉注射)。在随后的实验中,停止注射尼古丁,仅通过刺激的偶然呈现来强化响应。去除尼古丁一个月后,将大麻素CB1受体拮抗剂利莫那班双侧注射到伏隔核壳(ShNAcc,0.3、3或30ng/0.5微升)、基底外侧杏仁核(BLA,30ng/0.5微升)或前边缘皮层(PLCx,30ng/0.5微升)。
注射到ShNAcc的利莫那班剂量依赖性地减少了尼古丁寻求行为,而不改变自发运动活动。当将该药物(30ng)注射到BLA或PLCx时也获得了类似结果。在使用[³H]利莫那班的对照实验中证实了解剖学特异性。药物注射后15分钟,当利莫那班的行为效应已经出现时,在注射部位检测到放射性,且未扩散到相邻区域。
这些发现表明,内源性大麻素传递增加在关键皮质-边缘区域中关键地触发了条件性尼古丁寻求行为。