Cannabinoid receptors in the basolateral amygdala are involved in the potentiation of morphine rewarding properties in the acquisition, but not expression of conditioned place preference in rats

被引:13
|
作者
Haghparast, Abbas [1 ]
Shamsizadeh, Ali [2 ]
Samandari, Razieh [1 ]
Omranifard, Alireza [1 ]
Vaziri, Anoumid [1 ]
Razavi, Yasaman [2 ]
机构
[1] Shahid Beheshti Univ Med Sci, Neurosci Res Ctr, Fac Med, Tehran, Iran
[2] Rafsanjan Univ Med Sci, Physiol Pharmacol Res Ctr, Rafsanjan, Iran
关键词
Reward; Cannabinoid receptor; Basolateral amygdala; Morphine; Conditioned place preference; Rat; VENTRAL TEGMENTAL AREA; NUCLEUS-ACCUMBENS; CB1; RECEPTORS; DOPAMINE; CONSOLIDATION; ANTAGONIST; MODULATION; RELEASE; NMDA;
D O I
10.1016/j.brainres.2014.04.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Several studies show the role of the basolateral amygdala (BLA) in drug-seeking, relapse and the brain's emotional systems. Several lines of evidence indicate a functional interaction between opioid and endogenous cannabinoid systems. In the present study, we investigated the role of intra-BLA cannabinoid CB1 receptors in the potentiation, acquisition and expression of morphine-induced conditioned place preference (CPP). One-hundred and forty-two adult male Wistar rats weighing 230-280 g were bilaterally implanted by two separate cannulae into the BLA. The CPP paradigm was done, and conditioning score and locomotor activity were recorded by Ethovision software. Results showed that intra-BLA administration of different doses of WIN55,212-2 (1, 2 and 4 mmol/0.3 mu l DMSO) as a cannabinoid receptor agonist during the conditioning phase induced place preference in animals that received the ineffective (2 mg/kg) dose of morphine compared to respective control group in saline-treated animals. On the other hand, intra-BLA injection of the cannabinoid CB1 receptor antagonist AM251 (45 and 90 mu mol/0.3 mu l DMSO) during the 3-day conditioning phase reduced morphine-induced CPP. Furthermore, microinjection of both AM251 (15, 45 and 90 mu mol) and WIN55,212-2 (1-4 mmol), into the BLA had no effect on the expression of morphine (5 mg/kg)-induced CPP. Our findings suggest that cannabinoid CB1 receptors in the BLA are involved in the development of reward-related behaviors and they can potentiate the rewarding effects of morphine. It seems that the glutamatergic projection from the BLA to the nucleus accumbens and reward-related learning in the hippocampus may be involved in the acquisition and expression of opioid reward-related behaviors in rats. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 36
页数:9
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