The Children's Hospital of Philadelphia, Abramson Research Center, 3615 Civic Center Boulevard, Philadelphia, Pennsylvania 19104, USA.
Endocrinology. 2010 Apr;151(4):1795-805. doi: 10.1210/en.2009-1026. Epub 2010 Feb 16.
Previous social stress exposure is a common risk factor for affective disorders. However, factors that determine vulnerability or resiliency to social stress-induced psychopathologies remain unclear. Using a rodent model of social stress, the present study was designed to identify putative neurobiological substrates that contribute to social stress-induced psychopathology and factors that influence or predict vulnerability. The resident-intruder model of defeat was used as a social stressor in adult male Sprague Dawley rats. The average latency to assume a subordinate posture (signaling defeat) over seven daily defeat exposures was calculated and examined with respect to endpoints of hypothalamic-pituitary-adrenal activity, components of the corticotropin-releasing factor (CRF) system, and behaviors that are relevant to human depression. In the present studies, a bimodal distribution emerged in an otherwise homogeneous population of Sprague Dawley rats such that 42% of rats exhibited short defeat latencies (<300 sec), whereas 58% of rats resisted defeat and exhibited longer latencies (>300 sec). These two phenotypes were associated with distinct endocrine and behavioral profiles as well as differences in components of the CRF system. Notably, the short-latency subpopulation exhibited hypothalamic-pituitary-adrenal dysregulation and behavior similar to that observed in melancholic depression. Examination of components of the CRF system suggested that proactive behavior in resisting defeat exhibited by long-latency rats was associated with decreased efficacy of CRF. Together, these data suggest that inherent differences in stress reactivity, perhaps as a result of differences in CRF regulation, may predict long-term consequences of social stress and vulnerability to depressive-like symptoms.
先前的社会压力暴露是情感障碍的常见危险因素。然而,决定对社会压力引起的精神病理易感性或弹性的因素仍不清楚。本研究使用社会压力的啮齿动物模型,旨在确定可能有助于社会压力引起的精神病理的神经生物学基础,以及影响或预测易感性的因素。采用成年雄性 Sprague Dawley 大鼠的社交挫败模型作为社会应激源。计算了在七次每日挫败暴露中,大鼠采取从属姿势(表示挫败)的平均潜伏期,并针对下丘脑-垂体-肾上腺活性的终点、促肾上腺皮质激素释放因子 (CRF) 系统的组成部分,以及与人类抑郁相关的行为进行了检查。在本研究中,一种双峰分布出现在 Sprague Dawley 大鼠的一个原本均匀的群体中,其中 42%的大鼠表现出短的挫败潜伏期(<300 秒),而 58%的大鼠则抵抗挫败并表现出更长的潜伏期(>300 秒)。这两种表型与明显不同的内分泌和行为特征以及 CRF 系统的组成部分的差异有关。值得注意的是,短潜伏期亚群表现出下丘脑-垂体-肾上腺失调,其行为类似于忧郁性抑郁症所观察到的行为。对 CRF 系统组成部分的检查表明,长潜伏期大鼠表现出的抵抗挫败的主动行为与 CRF 效力的降低有关。总的来说,这些数据表明,应激反应的固有差异,可能是由于 CRF 调节的差异,可能预测社会压力的长期后果和抑郁样症状的易感性。