Department of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Institute of Neuroscience and The Collaborative Innovation Center for Brain Science, Chongqing Medical University, Chongqing, China.
Transl Psychiatry. 2018 Jan 10;8(1):4. doi: 10.1038/s41398-017-0018-1.
Major depressive disorder (MDD) is a heterogeneous and multi-factorial disorder, and the underlying molecular mechanisms remain largely unknown. However, many studies have indicated that the molecular mechanisms underlying depression in response to different stress may differ. After screening, 28-30 rats were included in each model of depression (chronic unpredictable mild stress (CUMS); learned helplessness (LH); chronic restraint stress (CRS); or social defeat (SD)). Non-targeted gas chromatography-mass spectrometry was used to profile the metabolic changes in the hippocampus. As a result, all four models exhibited significant depression-like behavior. A total of 30, 24, 19, and 25 differential metabolites were identified in the CUMS, LH, CRS, and SD models, respectively. Interestingly, the hierarchical clustering results revealed two patterns of metabolic changes that are characteristic of the response to cluster 1 (CUMS, LH) and cluster 2 (CRS, SD) stress, which represent physical and psychological stress, respectively. Bioinformatic analysis suggested that physical stress was mainly associated with lipid metabolism and glutamate metabolism, whereas psychological stress was related to cell signaling, cellular proliferation, and neurodevelopment, suggesting the molecular changes induced by physical and psychological stress were different. Nine shared metabolites were opposite in the directions of change between physical and psychological models, and these metabolites were associated with cellular proliferation and neurodevelopment functions, indicating the response to physical and psychological stress was different in the activation and deactivation of the final common pathway to depression. Our results provide a further understanding of the heterogeneity in the molecular mechanisms of MDD that could facilitate the development of personalized medicine for this disorder.
重度抑郁症(MDD)是一种异质性和多因素疾病,其潜在的分子机制在很大程度上仍不清楚。然而,许多研究表明,不同应激源引起的抑郁的潜在分子机制可能不同。筛选后,每个抑郁模型(慢性不可预测轻度应激(CUMS);习得性无助(LH);慢性束缚应激(CRS);或社交挫败(SD))中均纳入了 28-30 只大鼠。非靶向气相色谱-质谱法用于分析海马代谢变化。结果,所有四种模型均表现出明显的抑郁样行为。在 CUMS、LH、CRS 和 SD 模型中分别鉴定出 30、24、19 和 25 个差异代谢物。有趣的是,层次聚类结果显示出两种代谢变化模式,这两种模式分别与对聚类 1(CUMS、LH)和聚类 2(CRS、SD)应激的反应有关,分别代表身体和心理应激。生物信息学分析表明,身体应激主要与脂质代谢和谷氨酸代谢有关,而心理应激与细胞信号、细胞增殖和神经发育有关,表明身体和心理应激引起的分子变化不同。9 个共享代谢物在身体和心理模型之间的变化方向相反,这些代谢物与细胞增殖和神经发育功能有关,表明身体和心理应激对抑郁最终共同途径的激活和失活的反应不同。我们的研究结果进一步了解了 MDD 分子机制的异质性,这有助于为这种疾病开发个性化医学。