Departments of Psychology and Neuroscience and Behavior, Barnard College of Columbia University, New York, NY, USA.
Stress. 2021 Sep;24(5):496-503. doi: 10.1080/10253890.2021.1873945. Epub 2021 Feb 15.
Stress-related psychological dysfunctions show a marked increase during adolescence, yet the mechanisms that mediate these vulnerabilities are unknown. Notably, however, adolescence is associated with changes in hormonal stress reactivity mediated by the hypothalamic-pituitary-adrenal (HPA) axis, which might contribute to these dysfunctions. Specifically, pre-adolescent animals display prolonged stress-induced HPA responses compared to adults. Previous experience with stressors further modify these changes in stress reactivity, such that repeated exposure to the same stressor results in an augmented HPA response prior to adolescence, but a habituated response in adulthood. It is unclear when during adolescence the habituated, adult-like response develops to a repeated stressor. Using male rats at various ages that span adolescence (30-70 days of age), we show that by mid-adolescence (i.e. 42 days of age), animals show neither a facilitated nor a habituated HPA hormonal response following four days of repeated restraint stress (4RS) compared to a single restraint session (1RS). We also show that the habituated HPA response to 4RS develops between late-adolescence and young adulthood (i.e. between 56 and 70 days of age, respectively). Further, we find age- and experience-dependent changes in progesterone and testosterone secretion, indicating that the interaction between development and experience affects stress-induced hormonal responses outside of canonical HPA-related hormones. Despite these hormonal differences mediated by age and experience, repeated restraint stress resulted in decreased fecal boli production at all four ages, suggesting dissociation between hormonal and autonomic reactivity during adolescence. These data indicate that HPA plasticity is significantly affected by adolescence and that a habituated hormonal response to homotypic stress does not occur until young adulthood. A greater appreciation of these changes in stress reactivity will contribute to our understanding of the psychological vulnerabilities often associated with stressful adolescence.
应激相关的心理功能障碍在青春期表现出明显增加,但其易感性的发生机制尚不清楚。然而,青春期与下丘脑-垂体-肾上腺(HPA)轴介导的激素应激反应变化有关,这可能是导致这些功能障碍的原因。具体而言,青春期前动物表现出比成年动物更长时间的应激诱导的 HPA 反应。先前经历的应激源进一步改变了这些应激反应的变化,使得重复暴露于相同的应激源会导致青春期前 HPA 反应增强,但成年期则出现习惯化反应。目前尚不清楚青春期何时会对重复的应激源产生习惯化的成人样反应。本研究使用跨越青春期(30-70 天龄)的各个年龄段的雄性大鼠,结果表明,到青春期中期(即 42 天龄),与单次束缚应激(1RS)相比,动物在经历四天重复束缚应激(4RS)后,HPA 激素反应既没有增强也没有习惯化。我们还表明,4RS 引起的 HPA 习惯化反应发生在青春期晚期和成年早期之间(分别为 56 和 70 天龄)。此外,我们发现年龄和经验依赖性的孕激素和睾酮分泌变化,表明发育和经验之间的相互作用会影响非典型 HPA 相关激素以外的应激诱导激素反应。尽管这些由年龄和经验介导的激素差异存在,但重复束缚应激会导致所有四个年龄段的粪便产量减少,这表明在青春期期间,激素和自主反应之间存在分离。这些数据表明 HPA 可塑性受到青春期的显著影响,并且对同型应激的习惯化激素反应直到成年早期才会发生。对这些应激反应变化的进一步认识将有助于我们理解与压力青春期相关的心理脆弱性。