Department of Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Universiteitssingel 50, NL 6229 ER Maastricht, Netherlands.
Prog Neuropsychopharmacol Biol Psychiatry. 2010 Mar 17;34(2):348-61. doi: 10.1016/j.pnpbp.2009.12.014. Epub 2009 Dec 22.
Many studies with chronic stress, a common depression paradigm, lead to inconsistent behavioral results. We are introducing a new model of stress-induced anhedonia, which provides more reproducible induction and behavioral measuring of depressive-like phenotype in mice. First, a 4-week stress procedure induces anhedonia, defined by decreased sucrose preference, in the majority of but not all C57BL/6 mice. The remaining 30-50% non-anhedonic animals are used as an internal control for stress effects that are unrelated to anhedonia. Next, a modified sucrose test enables the detection of inter-individual differences in mice. Moreover, testing under dimmed lighting precludes behavioral artifacts caused by hyperlocomotion, a major confounding factor in stressed mice. Finally, moderation of the stress load increases the reproducibility of anhedonia induction, which otherwise is difficult to provide because of inter-batch variability in laboratory mice. We believe that our new mouse model overcomes some major difficulties in measuring behavior with chronic stress depression models.
许多关于慢性应激的研究,作为一种常见的抑郁模型,导致了不一致的行为结果。我们引入了一种新的应激诱导快感缺失模型,该模型在小鼠中提供了更可重复的抑郁表型诱导和行为测量。首先,一个 4 周的应激程序导致大多数但不是所有 C57BL/6 小鼠出现快感缺失,表现为蔗糖偏好降低。剩下的 30-50%无快感缺失的动物被用作与快感缺失无关的应激效应的内部对照。接下来,改良的蔗糖测试能够检测小鼠个体间的差异。此外,在昏暗的灯光下进行测试可以避免由过度活跃引起的行为假象,这是应激小鼠的一个主要混杂因素。最后,适度减轻应激负荷可以提高快感缺失诱导的可重复性,否则由于实验室小鼠批次间的差异,很难提供这种可重复性。我们相信,我们的新小鼠模型克服了使用慢性应激抑郁模型测量行为的一些主要困难。