[基于串联质谱蛋白质组学技术的针刺改善cms诱导大鼠抑郁的机制研究]。

Ran Liu, Kun Zhang, Wen-Li Wang, Qiu-Yu Tong, Wen Ma, Wa Cai, Wei-Dong Shen
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引用次数: 0

摘要

目的:应用串联质量标签(TMT)定量蛋白质组学技术,探讨“调气解郁”针刺对慢性不可预知轻度应激(CUMS)大鼠抑郁症的改善作用机制。方法:将36只雄性SD大鼠随机分为对照组、模型组和针刺组,每组12只。CUMS胁迫诱导小鼠抑郁21 d。抑郁模型建立成功后,针刺组大鼠在“百会”(GV20)和“印堂”(GV24+)处进行手动针刺刺激,每次20 min,每日1次,连续21 d。采用野外试验、糖水偏好试验和强迫游泳试验(FST)评价大鼠的行为变化。采用TMT定量蛋白质组学获得海马组织中的差异蛋白,分析相关信号通路富集情况,然后采用Western blot和免疫荧光方法验证差异蛋白通路。结果:行为学实验显示,在第21天和第42天,水平穿越次数、步行距离和糖水消耗百分比均显著降低(ppppppppppp)。结论:针刺“调气解郁”可显著改善cms诱导的抑郁模型大鼠的抑郁样行为,其作用涉及多靶点、多通路,包括MAPK/JNK信号通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Study on mechanisms of acupuncture underlying improvement of CUMS-induced depression in rats based on tandem mass spectrometry proteomics technique].

Objective: To investigate the possible mechanism of "regulating qi and relieving depression" acupuncture underlying improvement of chronic unpredictable mild stress (CUMS)-induced depression in rats by using Tandem Mass Tags(TMT) quantitative proteomics technique.

Methods: Thirty-six male SD rats were randomly divided into control, model and acupuncture groups, with 12 rats in each group. The depression model was induced by CUMS stress for 21 days. After the depression model was successfully established, the rats in the acupuncture group received manual acupuncture stimulation at "Baihui" (GV20) and "Yintang" (GV24+) for 20 min, once daily for 21 days. Open field test, sugar water preference test and forced swimming test (FST) were used to evaluate the behavioral changes. TMT quantitative proteomics was used to obtain differential proteins in the hippocampus tissue and related signaling pathways enrichment was analyzed, followed by verifying differential protein pathways by using Western blot and immunofluorescence methods.

Results: Behavior tests showed that on the 21st and 42nd days, the horizontal crossing times, walking distance and percentage of sugar water consumption were significantly decreased (P<0.05), while the immobility time of FST was obviously increased (P<0.05) in the model group relevant to the control group. After acupuncture intervention, the horizontal crossing times, walking distance and percentage of sugar water consumption were significantly increased (P<0.05), and the immobility time was apparently decreased (P<0.05) in the acupuncture group relevant to the model group. The TMT quantitative proteomics of hippocampus tissue displayed that of the 71 differential proteins (model group vs control group), 32 was down-regulated and 39 up-regulated in the model group; and among the above 71 differential proteins, there were 20 differential proteins between acupuncture group and model group, 15 down-regulated and 5 up-regulated in the acupuncture group (vs the model group). The expression of Mapk8ipl was up-regulated in the model group (vs the control group) and down-regulated in the acupuncture group (vs the model group). GO and KEGG enrichment analysis showed that these acupuncture-related differential proteins mainly involve the regulation of blood coagulation system, MAPK signaling pathway, etc. We selected the MAPK/JNK signaling pathway related to depression for verification. Western blot showed that the expression levels of c-JUN and phosphorylated c-JUN terminal kinase (p-JNK) proteins in the hippocampus were up-regulated in the model group relevant to the control group (P<0.05); while the expression levels of c-JUN and p-JNK proteins in the hippocampus were down-regulated in the acupuncture group relevant to the model group (P<0.05). The results of immunofluorescence showed that the mean fluorescence intensity of c-JUN and p-JNK in hippocampal CA1, CA3 and DG regions was increased in the model group relevant to the control group (P<0.05), while the mean fluorescence intensity of c-JUN and p-JNK in hippocampal CA1, CA3 and DG regions was obviously lower in the acupuncture group than in the model group (P<0.05).

Conclusion: Acupuncture for "regulating qi and relieving depression" can significantly improve depression-like behavior in CUMS-induced depression model rats, which involves multiple targets and multiple pathways, including MAPK/JNK signaling.

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