AMPHETAMINE SENSITIZATION IS ACCOMPANIED BY AN INCREASE IN PRELIMBIC CORTEX ACTIVITY

被引:15
|
作者
Aguilar-Rivera, M. I. [2 ]
Casanova, J. P. [2 ]
Gatica, R. I. [1 ,2 ]
Quirk, G. J. [3 ,4 ]
Fuentealba, J. A. [1 ,2 ]
机构
[1] Pontificia Univ Catolica Chile, Fac Chem, Dept Pharm, Santiago, Chile
[2] Pontificia Univ Catolica Chile, Santiago, Chile
[3] Univ Puerto Rico, Sch Med, Dept Psychiat, San Juan, PR 00936 USA
[4] Univ Puerto Rico, Sch Med, Dept Anat & Neurobiol, San Juan, PR 00936 USA
关键词
medial prefrontal cortex; amphetamine; locomotor sensitization; single-unit recording; MEDIAL PREFRONTAL CORTEX; DRUG-SEEKING BEHAVIOR; NUCLEUS-ACCUMBENS; COCAINE-SEEKING; UNRESTRAINED RATS; PYRAMIDAL NEURONS; FEAR EXTINCTION; DOPAMINE; ADDICTION; INHIBITION;
D O I
10.1016/j.neuroscience.2014.12.027
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Drug addiction is associated with dysfunction in the medial prefrontal cortex (mPFC). However, the modifications of neuronal activity in mPFC underlying the reinforcing properties of addictive drugs are still unclear. Here we carried out single-unit recording experiments to study the neuronal activity in the prelimbic (PL) cortex of anesthetized rats, after expression of locomotor sensitization to amphetamine. In control rats, an acute injection of amphetamine induced mainly an inhibitory effect on firing rate (FR) and this response was negatively correlated with the basal FR. Sensitized rats showed a higher proportion of excited neurons and the response to amphetamine was independent of basal FR. Moreover, in control rats, acute amphetamine decreased burst rate, whereas in sensitized rats acute amphetamine increased burst rate. These findings indicate that amphetamine sensitization renders mPFC neurons hyperexcitable. Taken together, these data support the hypothesis that early withdrawal is associated with an increase in the activity of the mPFC, which could strengthen the PL-Nucleus Accumbens connection, thus facilitating amphetamine-induced locomotor sensitization. (C) 2014 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 9
页数:9
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