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首页|期刊导航|中医学报|益气通脉方调控PI3K/AKT信号通路改善脑缺血再灌注损伤大鼠神经元凋亡

益气通脉方调控PI3K/AKT信号通路改善脑缺血再灌注损伤大鼠神经元凋亡

葛文静 陈芳芳 庞伯通 南淞华 秦阳 崔应麟

中医学报2024,Vol.39Issue(1):63-70,8.
中医学报2024,Vol.39Issue(1):63-70,8.DOI:10.16368/j.issn.1674-8999.2024.01.012

益气通脉方调控PI3K/AKT信号通路改善脑缺血再灌注损伤大鼠神经元凋亡

Yiqi Tongmai Formula Regulating PI3K/AKT Signaling Pathway to Improve Neuronal Apoptosis in Rats with Cerebral Ischemia-Reperfusion Injury

葛文静 1陈芳芳 2庞伯通 2南淞华 2秦阳 2崔应麟1

作者信息

  • 1. 河南中医药大学第二临床医学院,河南 郑州 450002||河南省中医药防治心脑血管病重点实验室,河南 郑州 450002
  • 2. 河南中医药大学第二临床医学院,河南 郑州 450002
  • 折叠

摘要

Abstract

Objective:Based on the signal pathway of phosphatidylinositol 3-kinases/protein kinase B(PI3K/AKT),to explore the mechanism of Yiqi Tongmai Formula on neural function damage and apoptosis in middle cerebral artery occlusion and reperfusion(MCAO/R)model rats.Method:Twelve healthy SPF grade male SD rats were selected as the sham surgery group from 68 individuals,while the remaining rats were used to prepare MCAO/R models using an improved suture method.36 successful MACO/R model rats were divided into model group,Yiqi Tongmai Formula group(1.08 g·kg-1)and Nimodipine tablet group(10.8 mg·kg-1),with12 rats in each group.The rats were given corresponding drug intervention,with a gastric lavage volume of 10 mL·kg-1 for 14 consecutive days,once a day.Rats in the sham surgery group and model group were given equal volumes of physiological saline by gavage.Use the Modified Neurological Severity Score(mNSS)method to evaluate the neural function of rats;HE staining was used to observe the mor-phological changes of brain tissue in each group of rats;TUNEL staining was used to detect cell apoptosis;Western blot was used to de-tect the protein expression levels of PI3K,p-PI3K,AKT,p-AKT,B cell lymphoma-2(Bcl-2),and Bcl-2 associated X genes(Bcl-2 associated X,Bax)in ischemic penumbra brain tissue;RT qPCR was used to detect the expression levels of Bax mRNA and Bcl-2 mRNA in rat brain tissue.Results:Compared with the sham surgery group,the mNSS score,neuronal apoptosis rate,relative ex-pression levels of Bax protein and genes in the model group rats were significantly increased(P<0.01),while the ratios of p-PI3K/PI3K and p-AKT/AKT were significantly down regulated(P<0.01).The relative expression levels of Bcl-2 protein and genes were significantly down regulated(P<0.01);Compared with the model group,the mNSS score of rats in the Yiqi Tongmai Formula group was significantly reduced(P<0.05)on the 3rd,7th,and 14th day,while the apoptosis rate of neurons,relative expression of Bax pro-tein and genes were significantly reduced(P<0.05).The ratio of p-PI3K/PI3K,p-AKT/AKT was significantly increased(P<0.01),and the relative expression levels of Bcl-2 protein and genes were significantly increased(P<0.01).HE staining showed that the number of nerve cells in the brain tissue of the model group rats was significantly reduced,the nuclei were pyknotic or disappeared,the cells were significantly ruptured,cavities and inflammatory cell infiltration were observed,some neurons were necrotic and degenera-ted,arranged irregularly,interstitial edema was observed,and the hierarchy was unclear.The number of brain tissue cells in the Yiqi Tongmai Formula group of rats significantly increased,the morphology of nuclear shrinkage improved,the number of cavities and inflam-matory factors decreased,interstitial edema decreased,and the number of degenerated and necrotic nerve cells significantly decreased.The morphology and structure of brain tissue cells were significantly restored.Conclusion:Yiqi Tongmai Formula can activate the PI3K/AKT signaling pathway,regulate the expression of downstream apoptosis related factors Bax and Bcl-2,and thus exert anti apoptotic and protective effects on damaged brain tissue after MCAO/R.

关键词

益气通脉方/PI3K/AKT信号通路/神经元细胞凋亡/脑缺血再灌注损伤

Key words

Yiqi Tongmai Formula/PI3K/AKT signaling pathway/neuron cell apoptosis/cerebral ischemia-reperfusion injury

分类

医药卫生

引用本文复制引用

葛文静,陈芳芳,庞伯通,南淞华,秦阳,崔应麟..益气通脉方调控PI3K/AKT信号通路改善脑缺血再灌注损伤大鼠神经元凋亡[J].中医学报,2024,39(1):63-70,8.

基金项目

河南省科技攻关计划项目(GZY-KSJ-2021-016,2023ZY1007) (GZY-KSJ-2021-016,2023ZY1007)

国家中医药管理局科研基金项目(212102311123) (212102311123)

中医学报

OACSTPCD

1674-8999

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