Ye Ran, Zhang Miao, Zhang Song, Bai Shasha, Jiang Zhangyu, Cai Qiang, Cao Kerun, Shen Chongkun, Shi Yafei, Zhang Rong, Yang Lei
School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 510000, P. R. China.
The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou 510000, P. R. China.
J Integr Neurosci. 2020 Mar 30;19(1):39-49. doi: 10.31083/j.jin.2020.01.1249.
Depression is a common mental health disorder that can impair normal functions, cause distress, and adversely affect the quality of life. Cognitive impairment is considered one of the characteristics of major depression disorders-related dysfunction, and it has received attention in the treatment of major depressive disorders. To investigated the mechanisms underlying depression-induced cognitive disorders, we selected a rodent model of chronic unpredictable mild stress and used liquid chromatography/mass spectrometry-based metabolomics of sera. Behavioral tests, including the sucrose preference test and open field test, revealed that model rats developed depression-like symptoms in the sixth week of the chronic unpredictable mild stress period. Rats of the model group exhibited significant cognitive changes in the Morris water maze test in the tenth week of the period. Tau phosphorylation and decreased levels of postsynaptic density-95 and synaptophysin were observed in the rodent brains by the tenth week. These results suggest that rodents developed cognitive impairment in the tenth week of the period, while serum metabonomic showed that glycerophospholipid metabolism is the most relevant pathway to reveal the mechanism of depression-induced cognitive impairment. The disorders of lipid metabolism caused by the increased cholesterol efflux and reduced reuptake could be one of the mechanisms of depression-induced cognitive disorders. However, the relationship between cholesterol efflux in the brain and elevated serum cholesterol needs further research.
抑郁症是一种常见的心理健康障碍,会损害正常功能,引发痛苦,并对生活质量产生不利影响。认知障碍被认为是重度抑郁症相关功能障碍的特征之一,并且在重度抑郁症的治疗中受到了关注。为了研究抑郁症诱发认知障碍的潜在机制,我们选择了慢性不可预测轻度应激的啮齿动物模型,并对血清进行基于液相色谱/质谱联用的代谢组学分析。行为测试,包括蔗糖偏好测试和旷场试验,显示模型大鼠在慢性不可预测轻度应激期的第6周出现了类似抑郁的症状。在该时期的第10周,模型组大鼠在莫里斯水迷宫试验中表现出显著的认知变化。到第10周时,在啮齿动物大脑中观察到tau蛋白磷酸化以及突触后致密蛋白-95和突触素水平降低。这些结果表明,啮齿动物在该时期的第10周出现了认知障碍,而血清代谢组学显示甘油磷脂代谢是揭示抑郁症诱发认知障碍机制最相关的途径。胆固醇外流增加和再摄取减少导致的脂质代谢紊乱可能是抑郁症诱发认知障碍的机制之一。然而,大脑中胆固醇外流与血清胆固醇升高之间的关系需要进一步研究。