Lin Tianwei, Dang Shaokang, Su Qian, Zhang Huiping, Zhang Junli, Zhang Lin, Zhang Xiaoxiao, Lu Yong, Li Hui, Zhu Zhongliang
Shaanxi Province Biomedicine Key Laboratory, College of Life Sciences, Northwest University, Xi'an 710069, Shaanxi, China.
Department of Pharmacology, College of Medicine, Xi'an Jiaotong University, Xi'an 710061, Shaanxi, China.
J Clin Med. 2018 May 23;7(6):117. doi: 10.3390/jcm7060117.
An increasing number of epidemiological investigations and animal models research suggest that prenatal stress (PS) could cause depression-like behavior in the offspring, which is sex specific. However, the underlying mechanisms remain to be elucidated. This study is to investigate the promoter methylation of metabotropic glutamate receptor 1 (mGluR1) and metabotropic Glutamate Receptor 5 (mGluR5) gene modification on PS induced depression-like behavior in offspring rats (OR). PS models were established, with or without 5-aza-2′-deoxycytidine (5-azaD, decitabine) treatment. Animal behavior was assessed by the sucrose preference test (SPT), forced swimming test (FST), and open field test (OFT). The mRNA and protein expression levels of mGluR1 and mGluR5 in the hippocampus of offspring were detected with quantitative real-time PCR and Western blot analysis, respectively. The promoter methylation in the hippocampus of mGluR1 and mGluR5 OR were also analyzed. SPT showed significantly reduced sucrose preference in PS induced OR. FST showed significantly prolonged immobility time in PS induced OR. OFT showed significantly reduced central residence time in PS induced OR and no significantly influence in rearing as well as in frequency of micturition. Moreover, the mRNA, protein expression levels, and gene promoter methylation level of mGluR1 and mGluR5 in the hippocampus were significantly increased in the PS induced male OR, while no significantly influence in the PS induced female OR. Furthermore, the PS induced effects in male OR could be reversed by the microinjection of 5-azaD. In conclusion, our results showed that the promoter methylation of mGluR1 and mGluR5 gene modification is only involved in PS induced depression-like behavior in male OR in a sex-specific manner. These findings might contribute to the understanding of the disease pathogenesis and clinical treatment in future.
越来越多的流行病学调查和动物模型研究表明,产前应激(PS)可导致后代出现抑郁样行为,且具有性别特异性。然而,其潜在机制仍有待阐明。本研究旨在探讨代谢型谷氨酸受体1(mGluR1)的启动子甲基化以及代谢型谷氨酸受体5(mGluR5)基因修饰对PS诱导的仔鼠抑郁样行为的影响。建立PS模型,分别给予或不给予5-氮杂-2'-脱氧胞苷(5-azaD,地西他滨)处理。通过蔗糖偏好试验(SPT)、强迫游泳试验(FST)和旷场试验(OFT)评估动物行为。分别采用定量实时PCR和蛋白质免疫印迹分析检测仔鼠海马中mGluR1和mGluR5的mRNA和蛋白质表达水平。同时分析mGluR1和mGluR5仔鼠海马中的启动子甲基化情况。SPT显示,PS诱导的仔鼠蔗糖偏好显著降低。FST显示,PS诱导的仔鼠不动时间显著延长。OFT显示,PS诱导的仔鼠中央停留时间显著减少,而竖毛次数和排尿频率无显著影响。此外,PS诱导的雄性仔鼠海马中mGluR1和mGluR5的mRNA、蛋白质表达水平及基因启动子甲基化水平显著升高,而PS诱导的雌性仔鼠无显著影响。此外,微量注射5-azaD可逆转PS对雄性仔鼠的诱导作用。总之,我们的结果表明,mGluR1和mGluR5基因修饰的启动子甲基化仅以性别特异性方式参与PS诱导的雄性仔鼠抑郁样行为。这些发现可能有助于未来对该疾病发病机制和临床治疗的理解。