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논문 기본 정보

자료유형
학술저널
저자정보
Zhang Xiao-Qing (Liaoning University of Traditional Chinese Medicine Shenyang Liaoning ChinaLiaoning Provincial Majo) Wang Yi-He (Liaoning University of Traditional Chinese Medicine Shenyang Liaoning ChinaLiaoning Provincial Majo) Sun Li (Liaoning University of Traditional Chinese Medicine Shenyang Liaoning China) Dong Bao-Qiang (Liaoning University of Traditional Chinese Medicine Shenyang Liaoning ChinaLiaoning Provincial Majo) Sui Yue-Jiao (Liaoning University of Traditional Chinese Medicine Shenyang Liaoning ChinaLiaoning Provincial Majo) Dong Jia-Zi (Liaoning University of Traditional Chinese Medicine Shenyang Liaoning ChinaLiaoning Provincial Majo) Han Yang (Liaoning University of Traditional Chinese Medicine Shenyang Liaoning ChinaLiaoning Provincial Majo)
저널정보
대한약침학회 Journal of Acupuncture & Meridian Studies Journal of Acupuncture & Meridian Studies Vol.15 No.5
발행연도
2022.11
수록면
322 - 332 (11page)
DOI
10.51507/j.jams.2022.15.5.322

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Background: Electroacupuncture (EA) is a widely used traditional Chinese medicine method to manage various diseases, including cerebral ischemia-reperfusion injury (CIRI). Objectives: We assessed the neuroprotective effects of EA and examined its mechanism in a rat model of the middle cerebral artery occlusion-reperfusion (MCAO/R). The gait analysis was performed to evaluate the neuroprotective effects. Western blot and immunohistochemistry assays were carried out to determine the molecular mechanisms of EA. Methods: Male SD rats were randomly divided into the sham operation group, right MCAO/R group, and EA group. EA was administered every day (4/20 Hz, 10 min/1 d) at the following acupoints: Baihui (DU20), Yintang (EX-HN3), and Zusanli (ST36). Gait and motor function were analyzed from day 8 onward. Results: The plantar support and balance coordination of MCAO/R rats decreased, and the cellular structure of the ischemic penumbra was unclear. EA improved the gait dynamics of the rats, adjusted the cell structure, further activated astrocytes, and increased the expression and phosphorylation of phosphoinositide 3-kinase/protein kinase B (PI3K/PKB or AKT). Conclusion: EA promoted astrocyte-related effects in the rat model. Our findings suggest that the neuroprotective mechanism of EA may be related to the activation of the PI3K/ AKT signaling pathway. The intervention enhanced brain protection and improved motor functions.

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