首页> 美国卫生研究院文献>Frontiers in Cellular Neuroscience >Electroacupuncture Pretreatment Ameliorates PTSD-Like Behaviors in Rats by Enhancing Hippocampal Neurogenesis via the Keap1/Nrf2 Antioxidant Signaling Pathway
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Electroacupuncture Pretreatment Ameliorates PTSD-Like Behaviors in Rats by Enhancing Hippocampal Neurogenesis via the Keap1/Nrf2 Antioxidant Signaling Pathway

机译:电针预处理通过Keap1 / Nrf2抗氧化剂信号通路增强海马神经发生,改善大鼠的PTSD行为。

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摘要

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.
机译:电针(EA)预处理是一种针对多种脑部疾病的临床有用疗法。但是,它是否以及通过何种确切的分子机制改善了创伤后应激障碍(PTSD)仍不清楚。在本研究中,大鼠在暴露于增强的单次长时间应激(ESPS)之前连续七天接受EA刺激。焦虑感和恐惧学习行为;海马神经发生核因子红系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;在ESPS后第14天评估AMP活化激酶(AMPK)的活性。 EA预处理改善了ESPS治疗大鼠的海马神经发生,并改善了焦虑样行为。 EA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敲低Nrf2影响焦虑样行为和神经保护性标志物(BDNF,DCX)的表达,其方式类似于单独的ESPS,并削弱了EA预处理的神经保护作用。相反,Keap1敲低增加HO-1的表达,改善海马神经发生,并减轻PTSD样行为。总而言之,我们的结果表明,EA预处理可能通过调节keap1 / Nrf2抗氧化剂防御途径来改善ESSD诱发的焦虑样行为,并预防PTSD大鼠模型中的海马神经发生破坏。

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