Department of Acupuncture and Moxibustion, Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University, Beijing, China.
Department of Acupuncture and Moxibustion, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, China.
Neuroscience. 2018 May 21;379:281-291. doi: 10.1016/j.neuroscience.2018.03.029. Epub 2018 Mar 26.
Emerging evidence suggests that acupuncture treatment has anti-oxidative effects that affect cognitive impairment in vascular dementia (VD) rats. In the present study, we aimed to investigate whether thioredoxin-1 (Trx-1)/thioredoxin reductase-1 (TrxR-1) was involved in the beneficial effects of acupuncture. After 2-weeks of acupuncture treatment, Morris water maze (MWM), dihydroethidium (DHE) staining, Nissl staining and TdT-mediated dUTP nick end labeling (TUNEL) staining were used to assess the effects of acupuncture on cognitive function and hippocampal neuronal injury in two-vessel occlusion (2VO) model. The protein and mRNA levels of Trx-1 and TrxR-1, the activity of TrxR-1 as well as the phosphorylation of the apoptosis signal-regulating kinase 1 (ASK1)-c-Jun N-terminal kinase (JNK)/p38 pathway were measured by Western blot, real-time PCR analysis, TrxR-1 activity analysis and immunofluorescence (IF) staining respectively. We found that there were oxidative and apoptotic injury in the CA1 area, accompanied with the decreased expressions of Trx-1 and TrxR-1 in the hippocampus. Acupuncture ameliorated cognitive deficits caused by cerebral ischemic injury and inhibited oxidative stress and neuronal apoptotic injury in the hippocampus. Acupuncture also up-regulated the expressions of Trx-1 and TrxR-1, increased the activity of TrxR-1, accompanied with inhibiting the activation of the ASK1-JNK/p38 pathway. However, the effects of acupuncture on improving cognitive function, inhibiting oxidative stress and neuron apoptotic damage were blocked by Trx-1siRNA. In conclusion, these findings indicated that acupuncture treatment improved VD though anti-oxidative and anti-apoptotic mechanisms which involved the up-regulations of Trx-1/TrxR-1 and inhibitions of ASK1-JNK/p38 pathway.
新出现的证据表明,针刺治疗具有抗氧化作用,可影响血管性痴呆(VD)大鼠的认知障碍。在本研究中,我们旨在探讨硫氧还蛋白-1(Trx-1)/硫氧还蛋白还原酶-1(TrxR-1)是否参与了针刺的有益作用。经过 2 周的针刺治疗后,采用 Morris 水迷宫(MWM)、二氢乙啶(DHE)染色、尼氏染色和末端转移酶介导的 dUTP 缺口末端标记(TUNEL)染色评估针刺对 2 血管闭塞(2VO)模型中海马神经元损伤和认知功能的影响。通过 Western blot、实时 PCR 分析、TrxR-1 活性分析和免疫荧光(IF)染色分别测量 Trx-1 和 TrxR-1 的蛋白和 mRNA 水平、TrxR-1 的活性以及凋亡信号调节激酶 1(ASK1)-c-Jun N 末端激酶(JNK)/p38 途径的磷酸化。我们发现 CA1 区存在氧化和凋亡损伤,伴随着海马中 Trx-1 和 TrxR-1 的表达降低。针刺改善了脑缺血损伤引起的认知障碍,抑制了海马中的氧化应激和神经元凋亡损伤。针刺还上调了 Trx-1 和 TrxR-1 的表达,增加了 TrxR-1 的活性,同时抑制了 ASK1-JNK/p38 途径的激活。然而,Trx-1siRNA 阻断了针刺改善认知功能、抑制氧化应激和神经元凋亡损伤的作用。总之,这些发现表明,针刺治疗通过上调 Trx-1/TrxR-1 和抑制 ASK1-JNK/p38 途径来改善 VD,从而发挥抗氧化和抗凋亡作用。