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Selective increase of dopamine D3 receptor gene expression as a common effect of chronic antidepressant treatments
被引:142
作者:
Lammers, CH
Diaz, J
Schwartz, JC
Sokoloff, P
机构:
[1] Ctr Paul Broca, INSERM, U109, Unite Neurobiol & Pharmacol Mol, F-75014 Paris, France
[2] Univ Paris 05, Physiol Lab, F-75006 Paris, France
关键词:
depression;
antidepressant drug;
electroconvulsive shock;
mesolimbic dopaminergic system;
D O I:
10.1038/sj.mp.4000754
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The mesolimbic dopaminergic system is a neuroanatomical key structure for reward and motivation upon which previous studies indicated that antidepressant drugs exert a stimulatory influence, via still unknown neurobiological mechanisms, Here we examined the effects of chronic administration of antidepressants of several classes (amitriptyline, desipramine, imipramine, fluoxetine and tranylcypromine) and repeated electroconvulsive shock treatments (ECT) on dopamine D-3 receptor expression in the shell of the nucleus accumbens, a major projection area of the mesolimbic dopaminergic system, Short-term drug treatments had variable effects on D-3 receptor mRNA expression, In contrast, treatments for 21 days (with all drugs except fluoxetine) significantly increased D-3 receptor mRNA expression in the shell of nucleus accumbens; D-3 receptor binding was also significantly increased by amitriptyline or fluoxetine after a 42-day treatment, ECT for 10 days increased D-3 receptor mRNA and binding in the shell of nucleus accumbens. D-1 receptor and D-2 receptor mRNAs were increased by imipramine and amitriptyline, but not by the other treatments, The time-course of altered D-3 receptor expression, in line with the delayed clinical efficiency of antidepressant treatment, and the fact that various antidepressant drugs and ECT treatments eventually produced the same effects, suggest that increased expression of the D-3 receptor in the shell of nucleus accumbens is a common neurobiological mechanism of antidepressant treatments, resulting in enhanced responsiveness to the mesolimbic dopaminergic system.
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页码:378 / 388
页数:11
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