Department of Physiology, Seoul National University College of Medicine, Seoul 110-799, Korea. ; Neuroscience Research Institute, Seoul National University Medical Research Center, Seoul 110-799, Korea.
Department of Pharmacology, Seoul National University College of Medicine, Seoul 110-799, Korea.
Korean J Physiol Pharmacol. 2014 Jun;18(3):263-8. doi: 10.4196/kjpp.2014.18.3.263. Epub 2014 Jun 12.
The etiology of most psychiatric disorders is still incompletely understood. However, growing evidence suggests that stress is a potent environmental risk factor for depression and anxiety. In rodents, various stress paradigms have been developed, but psychosocial stress paradigms have received more attention than non-social stress paradigms because psychosocial stress is more prevalent in humans. Interestingly, some recent studies suggest that chronic psychosocial stress and social isolation affects mainly anxiety-related behaviors in mice. However, it is unclear whether chronic non-social stress induces both depression- and anxiety-related phenotypes or induces one specific phenotype in mice. In the present study, we examined the behavioral consequences of three chronic non-social stress paradigms: chronic predictable (restraint) stress (CPS), chronic unpredictable stress (CUS), and repeated corticosterone-HBC complex injection (RCI). Each of the three paradigms induced mild to severe depression/despair-like behaviors in mice and resulted in increased immobility in a tail suspension test. However, anxiety-related phenotypes, thigmotaxis and explorative behaviors, were not changed by the three paradigms. These results suggest that depression- and anxiety-related phenotypes can be dissociated in mouse stress models and that social and non-social stressors might affect brain circuits and behaviors differently.
大多数精神疾病的病因仍不完全清楚。然而,越来越多的证据表明,压力是抑郁和焦虑的一个强有力的环境风险因素。在啮齿动物中,已经开发出了各种应激模型,但社会心理应激模型比非社会应激模型受到更多的关注,因为社会心理应激在人类中更为普遍。有趣的是,一些最近的研究表明,慢性社会心理应激和社会隔离主要影响小鼠的焦虑相关行为。然而,目前尚不清楚慢性非社会性应激是否会同时引起抑郁和焦虑相关表型,还是会在小鼠中引起一种特定的表型。在本研究中,我们研究了三种慢性非社会性应激模型的行为后果:慢性可预测(束缚)应激(CPS)、慢性不可预测应激(CUS)和重复皮质酮-HBC 复合物注射(RCI)。这三种范式都导致了小鼠轻度至重度的抑郁/绝望样行为,并导致在悬尾试验中不动性增加。然而,焦虑相关表型、触壁行为和探索行为并未被三种范式改变。这些结果表明,抑郁和焦虑相关表型可以在小鼠应激模型中分离,社会和非社会应激源可能以不同的方式影响大脑回路和行为。