Razzoli Maria, Carboni Lucia, Arban Roberto
Neurosciences CEDD, GlaxoSmithKline Medicine Research Centre, 37135 Verona, Italy.
Psychoneuroendocrinology. 2009 Oct;34(9):1405-16. doi: 10.1016/j.psyneuen.2009.04.018. Epub 2009 May 30.
In the realm of animal models of psychopathology, social stress based procedures rely on robust theoretical prerequisites to meet construct validity criteria for the target syndromes. In order to further assess the relevance for human psychopathology of a social defeat based model in rats, known to elicit consistent behavioral and hormonal changes, we expanded its characterization on the basis of both behavioral parameters and peripheral biomarkers thought to be pertinent for clinical symptoms. Rats were subjected to 3 daily social defeat experiences that shortly thereafter led to the insurgence of defensive behaviors, anhedonia, and body weight loss. HPA axis showed an activated response when rats were sampled as early as after the first social defeat experience, while none of the peripheral immune, metabolic, and neurotrophic factors examined were concurrently affected. With the aim of determining the long-term bio-behavioral sequelae of the social defeat experience, rats were assessed also 3 weeks after the social defeats. At this time, behavioral changes were still observed, including decreased general activity and sociality in a social avoidance test, increased immobility and decreased escape responses in a forced swim test. These alterations were not paralleled by alterations in anhedonia nor HPA axis responses from controls, nor where evident changes in the humoral component of the immune response nor in brain derived neurotrophic factor levels, whereas a substantial increase in leptin levels was observed in previously socially defeated rats compared to control. Overall these data depict a very complex set of alterations induced both acutely and long-term by social stress in endocrinological and behavioral reactivity of rats.
在精神病理学动物模型领域,基于社会应激的实验程序依赖于坚实的理论前提,以满足目标综合征的结构效度标准。为了进一步评估大鼠中基于社会挫败的模型与人类精神病理学的相关性,已知该模型会引发一致的行为和激素变化,我们基于行为参数和被认为与临床症状相关的外周生物标志物对其进行了扩展表征。大鼠每天经历3次社会挫败,此后不久便出现防御行为、快感缺失和体重减轻。早在第一次社会挫败经历后对大鼠进行采样时,下丘脑-垂体-肾上腺(HPA)轴就显示出激活反应,而所检测的外周免疫、代谢和神经营养因子均未同时受到影响。为了确定社会挫败经历的长期生物行为后遗症,在社会挫败3周后也对大鼠进行了评估。此时,仍观察到行为变化,包括在社会回避测试中总体活动和社交性降低,在强迫游泳测试中不动时间增加和逃避反应减少。这些改变与对照组的快感缺失或HPA轴反应的改变并不平行,免疫反应的体液成分或脑源性神经营养因子水平也没有明显变化,而与对照组相比,先前经历社会挫败的大鼠瘦素水平显著升高。总体而言,这些数据描绘了社会应激在大鼠内分泌和行为反应性中急性和长期诱导的一组非常复杂的变化。