Godar Sean C, Bortolato Marco
Department of Pharmacology and Toxicology, School of Pharmacy, University of Kansas Lawrence, KS, USA.
Department of Pharmacology and Toxicology, School of Pharmacy, University of Kansas Lawrence, KS, USA ; Consortium for Translational Research on Aggression and Drug Abuse, University of Kansas Lawrence, KS, USA.
Front Behav Neurosci. 2014 Mar 6;8:71. doi: 10.3389/fnbeh.2014.00071. eCollection 2014.
Schizophrenia is a severe mental disorder, with a highly complex and heterogenous clinical presentation. Our current perspectives posit that the pathogenic mechanisms of this illness lie in complex arrays of gene × environment interactions. Furthermore, several findings indicate that males have a higher susceptibility for schizophrenia, with earlier age of onset and overall poorer clinical prognosis. Based on these premises, several authors have recently begun exploring the possibility that the greater schizophrenia vulnerability in males may reflect specific gene × sex (G×S) interactions. Our knowledge on such G×S interactions in schizophrenia is still rudimentary; nevertheless, the bulk of preclinical evidence suggests that the molecular mechanisms for such interactions are likely contributed by the neurobiological effects of sex steroids on dopamine (DA) neurotransmission. Accordingly, several recent studies suggest a gender-specific association of certain DAergic genes with schizophrenia. These G×S interactions have been particularly documented for catechol-O-methyltransferase (COMT) and monoamine oxidase (MAO), the main enzymes catalyzing DA metabolism. In the present review, we will outline the current evidence on the interactions of DA-related genes and sex-related factors, and discuss the potential molecular substrates that may mediate their cooperative actions in schizophrenia pathogenesis.
精神分裂症是一种严重的精神障碍,临床表现高度复杂且具有异质性。我们目前的观点认为,这种疾病的致病机制在于复杂的基因×环境相互作用。此外,一些研究结果表明,男性患精神分裂症的易感性更高,发病年龄更早,临床预后总体更差。基于这些前提,一些作者最近开始探讨男性精神分裂症易感性更高可能反映特定基因×性别(G×S)相互作用的可能性。我们对精神分裂症中这种G×S相互作用的了解仍然很初步;然而,大量临床前证据表明,这种相互作用的分子机制可能是由性类固醇对多巴胺(DA)神经传递的神经生物学效应所致。因此,最近的几项研究表明某些多巴胺能基因与精神分裂症存在性别特异性关联。这些G×S相互作用在儿茶酚-O-甲基转移酶(COMT)和单胺氧化酶(MAO)这两种催化DA代谢的主要酶中已有特别记载。在本综述中,我们将概述目前关于DA相关基因与性别相关因素相互作用的证据,并讨论可能介导它们在精神分裂症发病机制中协同作用的潜在分子底物。