Increased mRNA expression of α2A-adrenoceptors, serotonin receptors and μ-opioid receptors in the brains of suicide victims

被引:103
作者
Escribá, PV [1 ]
Ozaita, A [1 ]
García-Sevilla, JA [1 ]
机构
[1] Univ Balearic Isl, Neuropharmacol Lab, Associated Unit,Cajal Inst, CSIC,Dept Biol,Inst Univ Invest Ciencies Salut, Palma de Mallorca 07122, Spain
关键词
human brain; GPCR; neurotransmitter receptor; suicide;
D O I
10.1038/sj.npp.1300459
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The development of new therapies for the treatment of psychiatric disorders requires an in-depth knowledge of the molecular bases underlying these pathologies, which remain largely unknown. Alterations in adrenoceptors, serotonin receptors, and other G protein-coupled receptors (GPCRs) have been associated with suicide and depression. However, to date, there is little information about mRNA expression of the GPCRs in the frontal cortex of suicide victims. Our goal was to study the expression in the brain of these receptors. For this purpose, we measured mRNA levels by RT-PCR. We found that the expressions Of alpha(2A)-adrenoceptors, 5-HT1A, 5-HT2A serotonin receptors, and mu-opioid receptors were elevated in the post-mortem brains of these suicide victims with respect to matched controls. Moreover, in the case of alpha(2A)-adrenoceptors (the only for which these data were available), a significant correlation was observed between the level of mRNA and protein quantified in the brain of the same subjects, indicating that protein synthesis of this receptor was not influenced by post-translational regulatory mechanisms. In addition, the degree of adrenoceptor and 5-HT receptor expressions appeared to be correlated in the brains of suicide victims and control subjects. Alterations in the expression of adrenoceptors, serotonin, and opioid receptors indicate that these signaling proteins might be related to the etiopathology of suicidal and depressive behaviors. Alternatively, such changes may represent adaptive mechanisms to compensate for other as yet unknown alterations. The results also suggest that these receptors could share common regulatory mechanisms.
引用
收藏
页码:1512 / 1521
页数:10
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