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[针刺通过抑制大鼠脑缺血后小胶质细胞极化和炎症反应改善神经功能]

[Acupuncture ameliorates neurological function by suppressing microglia polarization and inflammatory response after cerebral ischemia in rats].

作者信息

Zhang Hui-Yu, Zhao Yi-Jin, Zhang Pei-Jun, Guo Min-Fang, Yu Jing-Wen, Chai Zhi, Ma Cun-Gen, Song Li-Juan, Yu Jie-Zhong

机构信息

Institute of Brain Science, Shanxi Datong University, Datong 037009, Shanxi Province, China.

Key Laboratory of Benefiting Qi to Activate Blood Circulation for Treating Multiple Sclerosis, State Administration of Traditional Chinese Medicine/Research Center of Neurobiology, Shanxi University of Chinese Medicine, Jinzhong 030619, Shanxi Province.

出版信息

Zhen Ci Yan Jiu. 2022 Nov 25;47(11):941-48. doi: 10.13702/j.1000-0607.20210988.

Abstract

OBJECTIVE

To observe the effect of acupuncture on microglia polarization and inflammatory reaction in rats with cerebral ischemia-reperfusion injury (CIRI), so as to explore its mechanisms underlying improvement of CIRI.

METHODS

Thirty male SD rats were randomly divided into sham operation, model, and acupuncture groups, with 10 rats in each group. The CIRI model was established by occlusion of the middle cerebral artery (MCAO) for 1 h, followed by reperfusion. After modeling, rats in the acupuncture group received manual acupuncture stimulation of "Dazhui" (GV14), "Baihui"(GV20), "Shuigou" (GV26), bilateral "Zusanli" (ST36) and "Fengchi" (GB20) by twirling the needles rapidly for 10 s/acupoint every 10 min, with the needles retained for 20 min. The treatment was conducted once daily for successive 7 days. The neurological function was evaluated according to Longa's method. The state of CIRI was observed after Nissl staining, and the expression levels of Iba-1, iNOS, Arg1, BDNF, GDNF and NeuN in the ischemic cortex tissue were detected by immunofluorescence staining. The contents of TNF-α, IL-6 and IL-10 in the ischemic tissue were assayed by ELISA. The protein expression levels of BDNF, GDNF, TLR4, MyD88 and NF-κB in the ischemic tissues were detected by Western blot.

RESULTS

The neurological deficit score on the 24 h and 7th day was considerably higher in the model group than in the sham operation group (<0.01), and evidently lower on the 7th day in the acupuncture group than in the model group (<0.01). The number of NeuN positive cells,the area of immunofluorescence dual labelling of Arg1, BDNF and GDNF positive staining, IL-10 content, BDNF and GDNF protein expressions were significantly decreased (<0.01), and the immunofluorescence dual labelling area of Iba-1 and iNOS, TNF-α and IL-6 contents, the pretein expression levels of TLR4, MyD88 and NF-κB considerably increased (<0.01) in the model group relevant to the sham operation group. In contrast to the model group, the acupuncture group had a significant increase in the number of NeuN positive cells, the immunofluorescence dual labelling area of Arg1, BDNF and GDNF positive staining, IL-10 content, and BDNF and GDNF protein expressions (<0.05, <0.01), and an evident decrease in Iba-1 and iNOS positive staining, contents of TNF-α and IL-6, and the protein expression levels of TLR4, MyD88 and NF-κB (<0.01, <0.05). Nissl staining showed a marked reduction in the number of neurons, the nucleus pyknosis and nissl bodies and loose arrangement of the neuronal cells in the model group, which was relatively milder in the acupuncture group.

CONCLUSION

Acupuncture intervention can improve neurological function in CIRI rats, which may be related to its effects in regulating the polarization of microglia, reducing inflammatory reaction and increasing the secretion of neurotrophic factors in the brain, inhibiting TLR4/MyD88/NF-κB signaling pathway.

摘要

目的

观察针刺对脑缺血再灌注损伤(CIRI)大鼠小胶质细胞极化及炎症反应的影响,以探讨其改善CIRI的作用机制。

方法

将30只雄性SD大鼠随机分为假手术组、模型组和针刺组,每组10只。采用大脑中动脉闭塞(MCAO)1 h再灌注的方法建立CIRI模型。造模后,针刺组大鼠取“大椎”(GV14)、“百会”(GV20)、“水沟”(GV26)、双侧“足三里”(ST36)及“风池”(GB20)穴,每10 min快速捻转提插针体10 s/穴,留针20 min,每日治疗1次,连续治疗7 d。采用Longa法评估神经功能。尼氏染色观察CIRI状态,免疫荧光染色检测缺血皮质组织中Iba-1、iNOS、Arg1、BDNF、GDNF及NeuN的表达水平。酶联免疫吸附测定(ELISA)法检测缺血组织中TNF-α、IL-6及IL-10含量。蛋白质免疫印迹法(Western blot)检测缺血组织中BDNF、GDNF、TLR4、MyD88及NF-κB蛋白表达水平。

结果

与假手术组比较,模型组大鼠在24 h及7 d时神经功能缺损评分显著升高(P<0.01),针刺组大鼠在7 d时神经功能缺损评分显著低于模型组(P<0.01)。与假手术组比较,模型组NeuN阳性细胞数、Arg1、BDNF及GDNF免疫荧光双标面积、IL-10含量、BDNF及GDNF蛋白表达显著降低(P<0.01),Iba-1及iNOS免疫荧光双标面积、TNF-α及IL-6含量、TLR4、MyD88及NF-κB蛋白表达显著升高(P<0.01)。与模型组比较,针刺组NeuN阳性细胞数、Arg1、BDNF及GDNF免疫荧光双标面积、IL-10含量、BDNF及GDNF蛋白表达显著升高(P<0.05,P<0.01),Iba-1及iNOS阳性染色、TNF-α及IL-6含量、TLR4、MyD88及NF-κB蛋白表达显著降低(P<0.01,P<0.05)。尼氏染色显示,模型组神经元数量明显减少,细胞核固缩,尼氏体减少,神经元细胞排列疏松,针刺组上述改变相对较轻。

结论

针刺干预可改善CIRI大鼠神经功能,其机制可能与调节小胶质细胞极化、减轻炎症反应、增加脑内神经营养因子分泌、抑制TLR4/MyD88/NF-κB信号通路有关。

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