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电针对脑缺血再灌注损伤中 NLRP3/ASC/Caspase-1 介导的 pyroptosis 的神经保护作用。

Electroacupuncture Ameliorates Neuronal Injury by NLRP3/ASC/Caspase-1 Mediated Pyroptosis in Cerebral Ischemia-Reperfusion.

机构信息

Department of Acupuncture-Moxibustion and Tuina, Qilu Hospital of Shandong University, Shandong University, No. 107 Wenhuaxi Road, Lixia District, Jinan, 250012, People's Republic of China.

Department of Acupuncture-Moxibustion, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.

出版信息

Mol Neurobiol. 2024 Apr;61(4):2357-2366. doi: 10.1007/s12035-023-03712-1. Epub 2023 Oct 24.

Abstract

NLRP3/ASC/Caspase-1 mediated pyroptosis is one of the important causes of cerebral ischemia-reperfusion (I/R) injury. Electroacupuncture (EA) is widely used in clinical treatment of ischemic stroke. However, mechanism of EA on ischemic stroke remains unclear. Therefore, on basis of a previous work, this study used middle cerebral artery occlusion (MCAO) 2 h and then reperfusion 7 days in rats to simulate brain I/R process. EA with Bahui (GV20) and Zusanli (ST36) and VX-765 (a specific inhibitor of Caspase-1) was performed. In this study, we found that EA improved cerebral infarct size and neuronal damage, including ultrastructural injury, and ameliorated nitro/oxidative stress in cerebral I/R. Additionally, EA treatment significantly decreased ASC, Caspase-1, GSDMD, and IL-1β expression and VX-765 treatment significantly decreased NLRP3, Caspase-1, and IL-1β expression. This proved that EA can regulate NLRP3/ASC/Caspase-1 mediated pyroptosis, improve neuronal injury during cerebral I/R, and provide basic experimental data for clinical treatment.

摘要

NLRP3/ASC/Caspase-1 介导的焦亡是脑缺血再灌注(I/R)损伤的重要原因之一。电针(EA)广泛应用于缺血性脑卒中的临床治疗。然而,EA 对缺血性脑卒中的作用机制尚不清楚。因此,本研究在先前工作的基础上,采用大脑中动脉闭塞(MCAO)2 h 后再灌注 7 d 的大鼠模型模拟脑 I/R 过程,观察电针百会(GV20)和足三里(ST36)结合 Caspase-1 特异性抑制剂 VX-765 对脑 I/R 的影响。本研究发现,EA 可改善脑梗死面积和神经元损伤,包括超微结构损伤,并减轻脑 I/R 中的氮/氧化应激。此外,EA 治疗可显著降低 ASC、Caspase-1、GSDMD 和 IL-1β 的表达,而 VX-765 治疗可显著降低 NLRP3、Caspase-1 和 IL-1β 的表达。这证明了 EA 可以调节 NLRP3/ASC/Caspase-1 介导的焦亡,减轻脑 I/R 期间的神经元损伤,为临床治疗提供了基础实验数据。

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