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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
来源:
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.
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页码:28 / 36
页数:9
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