van Luijtelaar Gilles, Onat Filiz Yilmaz, Gallagher Martin J
Donders Centre of Cognition, Radboud University Nijmegen, Nijmegen, The Netherlands.
Department of Pharmacology, School of Medicine, Marmara University, Istanbul, Turkey.
Neurobiol Dis. 2014 Dec;72 Pt B:167-79. doi: 10.1016/j.nbd.2014.08.014. Epub 2014 Aug 15.
While epidemiological data suggest a female prevalence in human childhood- and adolescence-onset typical absence epilepsy syndromes, the sex difference is less clear in adult-onset syndromes. In addition, although there are more females than males diagnosed with typical absence epilepsy syndromes, there is a paucity of studies on sex differences in seizure frequency and semiology in patients diagnosed with any absence epilepsy syndrome. Moreover, it is unknown if there are sex differences in the prevalence or expression of atypical absence epilepsy syndromes. Surprisingly, most studies of animal models of absence epilepsy either did not investigate sex differences, or failed to find sex-dependent effects. However, various rodent models for atypical syndromes such as the AY9944 model (prepubertal females show a higher incidence than prepubertal males), BN model (also with a higher prevalence in males) and the Gabra1 deletion mouse in the C57BL/6J strain offer unique possibilities for the investigation of the mechanisms involved in sex differences. Although the mechanistic bases for the sex differences in humans or these three models are not yet known, studies of the effects of sex hormones on seizures have offered some possibilities. The sex hormones progesterone, estradiol and testosterone exert diametrically opposite effects in genetic absence epilepsy and pharmacologically-evoked convulsive types of epilepsy models. In addition, acute pharmacological effects of progesterone on absence seizures during proestrus are opposite to those seen during pregnancy. 17β-Estradiol has anti-absence seizure effects, but it is only active in atypical absence models. It is speculated that the pro-absence action of progesterone, and perhaps also the delayed pro-absence action of testosterone, are mediated through the neurosteroid allopregnanolone and its structural and functional homolog, androstanediol. These two steroids increase extrasynaptic thalamic tonic GABAergic inhibition by selectively targeting neurosteroid-selective subunits of GABAA receptors (GABAARs). Neurosteroids also modulate the expression of GABAAR containing the γ2, α4, and δ subunits. It is hypothesized that differences in subunit expression during pregnancy and ovarian cycle contribute to the opposite effects of progesterone in these two hormonal states.
虽然流行病学数据表明,在人类儿童期和青春期起病的典型失神癫痫综合征中女性患病率较高,但在成人起病的综合征中,性别差异不太明显。此外,尽管被诊断为典型失神癫痫综合征的女性多于男性,但关于任何失神癫痫综合征患者发作频率和发作症状学的性别差异研究却很少。而且,非典型失神癫痫综合征的患病率或表现是否存在性别差异尚不清楚。令人惊讶的是,大多数失神癫痫动物模型研究要么没有调查性别差异,要么没有发现性别依赖性效应。然而,各种非典型综合征的啮齿动物模型,如AY9944模型(青春期前雌性发病率高于青春期前雄性)、BN模型(雄性患病率也较高)以及C57BL/6J品系中的Gabra1基因敲除小鼠,为研究性别差异所涉及的机制提供了独特的机会。尽管人类或这三种模型中性别差异的机制基础尚不清楚,但性激素对癫痫发作影响的研究提供了一些可能性。性激素孕酮、雌二醇和睾酮在遗传性失神癫痫和药理学诱发的惊厥性癫痫模型中发挥着截然相反的作用。此外,孕酮在发情前期对失神发作的急性药理作用与孕期所见相反。17β - 雌二醇具有抗失神发作作用,但仅在非典型失神模型中起作用。据推测,孕酮的促失神作用,可能还有睾酮的延迟促失神作用,是通过神经甾体别孕烯醇酮及其结构和功能类似物雄烷二醇介导的。这两种甾体通过选择性靶向GABAA受体(GABAARs)的神经甾体选择性亚基来增加突触外丘脑的紧张性GABA能抑制。神经甾体还调节含有γ2、α4和δ亚基的GABAAR的表达。据推测,孕期和卵巢周期中亚基表达的差异导致了孕酮在这两种激素状态下的相反作用。