Department of Integrative Physiology and Center for Neuroscience, University of Colorado Boulder, 1725 Pleasant Street, 114 Clare Small, Boulder, CO 80309-0354, USA.
Pflugers Arch. 2013 May;465(5):601-26. doi: 10.1007/s00424-013-1271-7. Epub 2013 Apr 16.
Research has elucidated causal links between stress exposure and the development of anxiety disorders, but due to the limited use of female or sex-comparative animal models, little is known about the mechanisms underlying sex differences in those disorders. This is despite an overwhelming wealth of evidence from the clinical literature that the prevalence of anxiety disorders is about twice as high in women compared to men, in addition to gender differences in severity and treatment efficacy. We here review human gender differences in generalized anxiety disorder, panic disorder, posttraumatic stress disorder and anxiety-relevant biological functions, discuss the limitations of classic conflict anxiety tests to measure naturally occurring sex differences in anxiety-like behaviors, describe sex-dependent manifestation of anxiety states after gestational, neonatal, or adolescent stressors, and present animal models of chronic anxiety states induced by acute or chronic stressors during adulthood. Potential mechanisms underlying sex differences in stress-related anxiety states include emerging evidence supporting the existence of two anatomically and functionally distinct serotonergic circuits that are related to the modulation of conflict anxiety and panic-like anxiety, respectively. We discuss how these serotonergic circuits may be controlled by reproductive steroid hormone-dependent modulation of crfr1 and crfr2 expression in the midbrain dorsal raphe nucleus and by estrous stage-dependent alterations of γ-aminobutyric acid (GABAergic) neurotransmission in the periaqueductal gray, ultimately leading to sex differences in emotional behavior.
研究已经阐明了应激暴露与焦虑障碍发展之间的因果关系,但由于女性或性比较动物模型的使用有限,因此对于这些障碍中性别差异的机制知之甚少。尽管临床文献中有大量证据表明,与男性相比,焦虑障碍的患病率女性约高出两倍,此外,在严重程度和治疗效果方面也存在性别差异。在这里,我们综述了广泛性焦虑障碍、惊恐障碍、创伤后应激障碍以及与焦虑相关的生物学功能方面的人类性别差异,讨论了经典冲突焦虑测试在测量焦虑样行为中自然发生的性别差异方面的局限性,描述了妊娠期、新生儿期或青春期应激后焦虑状态的性别依赖性表现,以及在成年期期间由急性或慢性应激引起的慢性焦虑状态的动物模型。应激相关焦虑状态的性别差异的潜在机制包括越来越多的证据支持存在两个解剖和功能上不同的 5-羟色胺能回路,它们分别与冲突焦虑和类似惊恐的焦虑的调节有关。我们讨论了这些 5-羟色胺能回路如何通过中脑背侧中缝核中 crfr1 和 crfr2 表达的生殖类固醇激素依赖性调节以及缰核中 γ-氨基丁酸(GABA 能)神经传递的发情期依赖性改变来控制,最终导致情绪行为中的性别差异。