Tunbridge Elizabeth M, Harrison Paul J
Department of Psychiatry, University of Oxford, Neurosciences Building, Warneford Hospital, Oxford, OX3 7JX, UK.
Curr Top Behav Neurosci. 2011;8:119-40. doi: 10.1007/7854_2010_97.
As outlined elsewhere in this volume, sex differences can affect brain function and its dysfunction in psychiatric disorders. It is known that genetic factors contribute to these sex dimorphisms, but the individual genes have rarely been identified. The catechol-O-methyltransferase (COMT) gene, which encodes an enzyme that metabolises catechol compounds, including dopamine, is a leading candidate in this regard. COMT's enzyme activity, and the neurochemistry and behaviour of COMT knockout mice are both markedly sexually dimorphic. Furthermore, genetic associations between COMT and psychiatric phenotypes frequently show differences between men and women. Although many of these differences are unconfirmed or minor, some appear to be of reasonable robustness and magnitude and are reviewed in this chapter. Sexually dimorphic effects of COMT are usually attributed to transcriptional regulation by oestrogens; however, a careful examination of the literature suggests that additional mechanisms are likely to be at least as important. Here, we review the evidence for a sexually dimorphic influence of COMT upon psychiatric phenotypes and brain function, and discuss potential mechanisms by which this may occur. We conclude that despite the evidence being incomplete, there are accumulating and in places compelling data showing that COMT has markedly sexually dimorphic effects on brain function and its dysfunction in psychiatric disorders. Although oestrogenic regulation of COMT is probably partially responsible for these sex differences, other mechanisms are likely also involved. Since sex differences in the genetic architecture of brain function and psychiatric disorders are the rule not the exception, we anticipate that additional evidence will emerge for sexual dimorphisms, not only in COMT but also in many other autosomal genes.
正如本卷其他地方所概述的,性别差异会影响大脑功能及其在精神疾病中的功能障碍。已知遗传因素促成了这些性别差异,但很少能确定具体的基因。儿茶酚-O-甲基转移酶(COMT)基因编码一种代谢儿茶酚化合物(包括多巴胺)的酶,在这方面是一个主要候选基因。COMT的酶活性以及COMT基因敲除小鼠的神经化学和行为都存在明显的性别差异。此外,COMT与精神疾病表型之间的遗传关联在男性和女性之间经常表现出差异。虽然其中许多差异未经证实或较小,但有些差异似乎具有合理的稳健性和幅度,本章将对此进行综述。COMT的性别差异效应通常归因于雌激素的转录调控;然而,仔细研究文献表明,其他机制可能至少同样重要。在这里,我们综述了COMT对精神疾病表型和大脑功能具有性别差异影响的证据,并讨论了其可能发生的潜在机制。我们得出结论,尽管证据不完整,但越来越多且在某些方面令人信服的数据表明,COMT对大脑功能及其在精神疾病中的功能障碍具有明显的性别差异效应。虽然雌激素对COMT的调控可能部分导致了这些性别差异,但其他机制可能也参与其中。由于大脑功能和精神疾病的遗传结构中的性别差异是普遍存在而非例外,我们预计不仅在COMT,而且在许多其他常染色体基因中,都会出现更多关于性别差异的证据。