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经皮耳迷走神经刺激对大脑中动脉栓塞模型大鼠缺血半暗带胶质纤维酸性蛋白及微管相关蛋白表达的影响
引用本文:赵敬军,李源莉,张金玲,任萌,徐菁菁,汪文静,周芷晴,王正辉,张英杰,单春雷.经皮耳迷走神经刺激对大脑中动脉栓塞模型大鼠缺血半暗带胶质纤维酸性蛋白及微管相关蛋白表达的影响[J].针刺研究,2022(1):33-38.
作者姓名:赵敬军  李源莉  张金玲  任萌  徐菁菁  汪文静  周芷晴  王正辉  张英杰  单春雷
作者单位:1.上海中医药大学康复医学院;2.上海中医药大学附属岳阳中西医结合医院;3.上海中医药大学教育部康复工程研究中心;4.中国中医科学院针灸研究所
基金项目:国家自然科学基金项目(No.81704163);国家科技重点研发计划项目(No.2018YFC2001600);上海市卫健委中医药三年行动计划项目(No.ZY2018-2020-CCCX-2001-06/2004-05)。
摘    要:目的:观察经皮耳迷走神经刺激(taVNS)对大脑中动脉栓塞(MCAO)模型大鼠运动功能及缺血半暗带胶质纤维酸性蛋白(GFAP)、微管相关蛋白2(MAP2)表达的影响,探讨taVNS改善MCAO模型大鼠运动功能的作用机制.方法:雄性SD大鼠随机分为假手术组、模型组、耳缘-非迷走神经刺激(tnVNS)组、taVNS组,每组...

关 键 词:缺血性脑卒中  星形胶质细胞  耳迷走神经刺激  胆碱能抗炎通路  神经保护

Effect of transcutaneous auricular vagus nerve stimulation on the expressions of GFAP and MAP2 in ischemic penumbra of rats with middle cerebral artery ischemia
ZHAO Jing-jun,LI Yuan-li,ZHANG Jin-ling,REN Meng,XU Jing-jing,WANG Wen-jing,ZHOU Zhi-qing,WANG Zheng-hui,ZHANG Ying-jie,SHAN Chun-lei.Effect of transcutaneous auricular vagus nerve stimulation on the expressions of GFAP and MAP2 in ischemic penumbra of rats with middle cerebral artery ischemia[J].Acupuncture Research,2022(1):33-38.
Authors:ZHAO Jing-jun  LI Yuan-li  ZHANG Jin-ling  REN Meng  XU Jing-jing  WANG Wen-jing  ZHOU Zhi-qing  WANG Zheng-hui  ZHANG Ying-jie  SHAN Chun-lei
Institution:,Rehabilitation Medicine College of Shanghai University of Traditional Chinese Medicine,Yueyang Integrated Chinese and Western Medicine Hospital, Shanghai University of Traditional Chinese Medicine,Rehabilitation Engineering Research Center of Education Administration, Shanghai University of Traditional Chinese Medicine,Institute of Acupuncture and Moxibustion, Chi
Abstract:Objective To observe the effects of transcutaneous auricular vagus nerve stimulation(taVNS) on the motor function and the expression of glial fibrillary acidic protein(GFAP) and microtubule associated protein 2(MAP2) in cerebral ischemic penumbra of rats with middle cerebral artery occlusion(MCAO) and explore the mechanism of taVNS in the improvement of motor function in MCAO rats. Methods A total of 48 male SD rats were randomized into a sham-operation group, a model group, a transcutaneous auricular non-vagus nerve stimulation(tnVNS) group and a taVNS group, with 12 rats in each group. The suture-occluded method was adopted to prepare MCAO rat model. The auricular rim was stimulated in the tnVNS group and the concha stimulated in the taVNS group, 2 mA in intensity, 10 Hz in frequency, 30 min each time, once a day, for 14 days consecutively. The nerve functional assessment was recorded in each group. The expressions of nicotinic acetylcholine receptor(α7 nAchR) in the cerebral ischemic penumbra and the spleen were detected by using Western blot. With the immunofluorescence, the expressions of GFAP and MAP2 were detected. Results After modeling, compared with the sham-operation group, the nerve functional score was increased in the model group, the tnVNS group and the taVNS group(P<0.01), suggesting the success of modeling. After treatment, the score was increased in the model group(P<0.01) as compared with the sham-operation group. Compared with the model group, the neurological deficit score was reduced in the taVNS group(P<0.01). Compared with the sham-operation group, GFAP expression was increased and MAP2 expression was reduced remarkably in the cerebral ischemic penumbra in the model group(P<0.05). In comparison with the model group, GFAP expression was reduced, while MAP2 expression was increased remarkably in the cerebral ischemic penumbra in the taVNS group(P<0.05). There were no significant differences in the abovementioned indexes between the model group and tnVNS group(P>0.05). The differences in the expression of α7 nAchR in the cerebral ischemic penumbra and the spleen had no statistical significance among groups(P>0.05). Conclusion TaVNS is effective on neuroprotection in MCAO rats, which may be related to its function of inhibition of GFAP expression and promotion of MAP2 expression in the ischemic penumbra.
Keywords:Ischemic stroke  Astrocytes  Transcutaneous auricular vagus nerve stimulation  Cholinergic anti-inflammatory pathway  Neuroprotection
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