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
Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Department of Anesthesiology, Xiang'an Hospital, Xiamen, China.
Front Cell Neurosci. 2019 Jun 21;13:275. doi: 10.3389/fncel.2019.00275. eCollection 2019.
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.
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。