Goel N, Bale T L
Department of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
J Neuroendocrinol. 2009 Mar;21(4):415-20. doi: 10.1111/j.1365-2826.2009.01843.x.
Sex-biased neuropsychiatric disorders, including major depressive disorder and schizophrenia, are the major cause of disability in the developed world. Elevated stress sensitivity has been proposed as a key underlying factor in disease onset. Sex differences in stress sensitivity are associated with corticotrophin-releasing factor (CRF) and serotonin neurotransmission, which are important central regulators of mood and coping responses. To elucidate the underlying neurobiology of stress-related disease predisposition, it is critical to develop appropriate animal models of stress pathway dysregulation. Furthermore, the inclusion of sex difference comparisons in stress responsive behaviours, physiology and central stress pathway maturation in these models is essential. Recent studies by our laboratory and others have begun to investigate the intersection of stress and sex where the development of mouse models of stress pathway dysregulation via prenatal stress experience or early-life manipulations has provided insight into points of developmental vulnerability. In addition, examination of the maturation of these pathways, including the functional importance of the organisational and activational effects of gonadal hormones on stress responsivity, is essential for determination of when sex differences in stress sensitivity may begin. In such studies, we have detected distinct sex differences in stress coping strategies where activational effects of testosterone produced females that displayed male-like strategies in tests of passive coping, but were similar to females in tests of active coping. In a second model of elevated stress sensitivity, male mice experiencing prenatal stress early in gestation showed feminised physiological and behavioural stress responses, and were highly sensitive to a low dose of selective serotonin reuptake inhibitors. Analyses of expression and epigenetic patterns revealed changes in CRF and glucocorticoid receptor genes in these mice. Mechanistically, stress early in pregnancy produced a significant sex-dependent effect on placental gene expression that was supportive of altered foetal transport of key growth factors and nutrients. These mouse models examining alterations and hormonal effects on development of stress pathways provide necessary insight into how specific stress responses can be reprogrammed early in development resulting in sex differences in stress sensitivity and neuropsychiatric disease vulnerability.
包括重度抑郁症和精神分裂症在内的性别偏见性神经精神疾病,是发达国家致残的主要原因。应激敏感性升高被认为是疾病发作的关键潜在因素。应激敏感性的性别差异与促肾上腺皮质激素释放因子(CRF)和5-羟色胺神经传递有关,它们是情绪和应对反应的重要中枢调节因子。为了阐明应激相关疾病易感性的潜在神经生物学机制,建立合适的应激途径失调动物模型至关重要。此外,在这些模型中纳入应激反应行为、生理学和中枢应激途径成熟度的性别差异比较也必不可少。我们实验室和其他机构最近的研究已开始探讨应激与性别的交叉点,通过产前应激经历或早期生活干预建立应激途径失调小鼠模型,为了解发育易损点提供了线索。此外,检查这些途径的成熟情况,包括性腺激素对应激反应性的组织和激活作用的功能重要性,对于确定应激敏感性的性别差异何时开始至关重要。在这类研究中,我们在应激应对策略中检测到明显的性别差异,睾酮的激活作用使雌性在被动应对测试中表现出类似雄性的策略,但在主动应对测试中与雌性相似。在另一个应激敏感性升高的模型中,妊娠早期经历产前应激的雄性小鼠表现出雌性化的生理和行为应激反应,并且对低剂量的选择性5-羟色胺再摄取抑制剂高度敏感。对表达和表观遗传模式的分析揭示了这些小鼠中CRF和糖皮质激素受体基因的变化。从机制上讲,妊娠早期的应激对胎盘基因表达产生了显著的性别依赖性影响,这支持了关键生长因子和营养物质胎儿转运的改变。这些研究应激途径发育变化及激素影响的小鼠模型,为了解特定应激反应如何在发育早期被重新编程从而导致应激敏感性和神经精神疾病易感性的性别差异提供了必要的见解。