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电针预处理通过Keap1/Nrf2抗氧化信号通路增强海马神经发生来改善大鼠的创伤后应激障碍样行为。

Electroacupuncture Pretreatment Ameliorates PTSD-Like Behaviors in Rats by Enhancing Hippocampal Neurogenesis via the Keap1/Nrf2 Antioxidant Signaling Pathway.

作者信息

Zhou Cui-Hong, Xue Fen, Xue Shan-Shan, Sang Han-Fei, Liu Ling, Wang Ying, Cai Min, Zhang Zhang-Jin, Tan Qing-Rong, Wang Hua-Ning, Peng Zheng-Wu

机构信息

Xijing Hospital, Fourth Military Medical University, Xi'an, China.

Department of Anesthesiology, Xiang'an Hospital, Xiamen, China.

出版信息

Front Cell Neurosci. 2019 Jun 21;13:275. doi: 10.3389/fncel.2019.00275. eCollection 2019.

Abstract

Electroacupuncture (EA) pretreatment is a clinically useful therapy for several brain disorders. However, whether and via which exact molecular mechanisms it ameliorates post-traumatic stress disorder (PTSD) remains unclear. In the present study, rats received EA stimulation for seven consecutive days before exposure to enhanced single prolonged stress (ESPS). Anxiety-like and fear learning behaviors; hippocampal neurogenesis; the expression of nuclear factor erythroid 2-related factor 2 (Nrf2), Kelch-like ECH-associated protein 1 (keap1), and heme oxygenase 1 (HO-1); and the activity of AMP-activated kinase (AMPK) were evaluated at 14 days after ESPS. EA pretreatment improved hippocampal neurogenesis and ameliorated anxiety-like behaviors in ESPS-treated rats. EA pretreatment also increased the expression of Nrf2 and HO-1 and the activity of AMPK. Furthermore, Nrf2 knockdown by a short hairpin RNA affected anxiety-like behaviors and expression of neuroprotective markers (BDNF, DCX) in a manner similar to ESPS alone and dampened the neuroprotective effects of EA pretreatment. In contrast, Keap1 knockdown increased the expression of HO-1, improved hippocampal neurogenesis, and alleviated PTSD-like behaviors. Altogether, our results suggest that EA pretreatment ameliorates ESPS-induced anxiety-like behaviors and prevents hippocampal neurogenesis disruption in a rat model of PTSD possibly through regulation of the keap1/Nrf2 antioxidant defense pathway.

摘要

电针预处理是治疗多种脑部疾病的一种临床有效疗法。然而,其是否以及通过何种确切分子机制改善创伤后应激障碍(PTSD)仍不清楚。在本研究中,大鼠在暴露于增强型单次长时间应激(ESPS)之前连续7天接受电针刺激。在ESPS后14天评估焦虑样和恐惧学习行为、海马神经发生、核因子红细胞2相关因子2(Nrf2)、 Kelch样ECH相关蛋白1(keap1)和血红素加氧酶1(HO-1)的表达,以及AMP激活的蛋白激酶(AMPK)的活性。电针预处理改善了ESPS处理大鼠的海马神经发生并减轻了焦虑样行为。电针预处理还增加了Nrf2和HO-1的表达以及AMPK的活性。此外,短发夹RNA介导的Nrf2敲低以类似于单独ESPS的方式影响焦虑样行为和神经保护标志物(BDNF、DCX)的表达,并减弱了电针预处理的神经保护作用。相反,Keap1敲低增加了HO-1的表达,改善了海马神经发生,并减轻了PTSD样行为。总之,我们的结果表明,电针预处理可能通过调节keap1/Nrf2抗氧化防御途径改善ESPS诱导的焦虑样行为,并防止PTSD大鼠模型中海马神经发生的破坏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3684/6598452/faca29231852/fncel-13-00275-g001.jpg

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