[Buyang Huanwu Decoction attenuates cerebral ischemia-reperfusion injury in rats via miR-26a-5p mediated PTEN/PI3K/Akt signaling pathway].

Q3 Pharmacology, Toxicology and Pharmaceutics Zhongguo Zhongyao Zazhi Pub Date : 2024-08-01 DOI:10.19540/j.cnki.cjcmm.20240515.501
Xiu-Hong Zhang, Kai-Long Fu, Kan Lin, Nan Li, Ming-Long Yao, Guan-Yi Zheng
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Abstract

This study aims to investigate the mechanism of Buyang Huanwu Decoction in treatment of cerebral ischemia-reperfusion injury in rats. A total of 180 SD rats were randomly divided into 5 different groups: sham group, model group, Buyang Huanwu Decoction group, Buyang Huanwu Decoction + miR-26a-5p agomir(agomir) group, Buyang Huanwu Decoction + miR-26a-5p agomir negative control(agomir NC) group. There were 36 rats in each group. Each group was then subdivided into three subgroups for the duration of reperfusion(3, 7, 14 d). A ligature-induced middle cerebral artery occlusion(MCAO) model was carried out on all groups other than sham group. Reperfusion was performed following ischemia for 90 min. Buyang Huanwu Decoction group, agomir group, and agomir NC group were given Buyang Huanwu Decoction twice daily by gavage 24 h after the formation of the model. Sham group and model group were given an equal amount of physiological saline by gavage until the day before sacrifice. At 24 h after ischemia induction, miR-26a-5p agomir was injected into the lateral ventricle in agomir group, miR-26a-5p NC in agomir NC group, and equal amounts of physiological saline in the other groups. 24 h after ischemia induction, BrdU was intraperitoneally injected once daily until the day before sacrifice. Modified neurological severity score(mNSS) was used to evaluate neurological deficits, 2,3,5-triphenyltetrazolium chloride(TTC) staining was used to determine the cerebral infarct volume, TUNEL staining was used to assess the apoptosis of parenchymal ischemic brain tissue, and double immunofluorescence staining was used to examine BrdU/NeuN double positive neurons in the parenchymal ischemic brain tissue to evaluate the neuronal regeneration. We employed a luciferase reporter assay to identify and validate that the target gene of miR-26a-5p is PTEN. Real-time quantitative polymerase chain reaction(RT-qPCR) was used to assess gene expression levels of PTEN and miR-26a-5p and Western blot to assess the protein levels of PTEN, PI3K, p-PI3K, Akt, and p-Akt. The results revealed that compared with model group, Buyang Huanwu Decoction treatment promoted neural function recovery, reduced the cerebral infarct volume, increased the number of BrdU~+/NeuN~+ neurons, upregulated the expression of miR-26a-5p, regulated the PTEN/PI3K/Akt signaling pathway, and promoted neuronal regeneration in the cerebral ischemia-reperfusion rats. These effects were significantly enhanced after lateral ventricle injection of miR-26a-5p agomir. The findings prove that Buyang Huanwu Decoction treatment can promote neural function recovery, reduce the cerebral infarct volume, and promote neuronal regeneration in a cerebral ischemia-reperfusion rat model, which is likely to be achieved via miR-26a-5p mediated PTEN/PI3K/Akt signaling pathway.

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[通过 miR-26a-5p 介导的 PTEN/PI3K/Akt 信号通路减轻大鼠脑缺血再灌注损伤】。]
本研究旨在探讨步阳黄酒煎剂治疗大鼠脑缺血再灌注损伤的机制。将180只SD大鼠随机分为5组:假组、模型组、步阳黄芪煎剂组、步阳黄芪煎剂+miR-26a-5p激动剂(激动剂)组、步阳黄芪煎剂+miR-26a-5p激动剂阴性对照(激动剂NC)组。每组 36 只大鼠。每组又按再灌注时间(3、7、14 d)分为三个亚组。除假组外,其他各组均采用结扎诱导的大脑中动脉闭塞(MCAO)模型。缺血 90 分钟后进行再灌注。模型形成 24 小时后,给布阳黄芪煎剂组、阿戈米尔组和阿戈米尔 NC 组灌胃布阳黄芪煎剂,每天两次。模型组和假体组在牺牲前一天灌胃等量生理盐水。缺血诱导24小时后,agomir组向侧脑室注射miR-26a-5p agomir,agomir NC组向侧脑室注射miR-26a-5p NC,其他各组注射等量生理盐水。缺血诱导 24 小时后,腹腔注射 BrdU,每天一次,直至牺牲前一天。改良神经严重程度评分(mNSS)用于评估神经功能缺损,2,3,5-三苯基氯化四氮唑(TTC)染色用于确定脑梗死体积,TUNEL染色用于评估缺血脑实质组织的凋亡,双重免疫荧光染色用于检测缺血脑实质组织中BrdU/NeuN双阳性神经元,以评估神经元再生情况。我们采用荧光素酶报告实验鉴定并验证了 miR-26a-5p 的靶基因是 PTEN。实时定量聚合酶链反应(RT-qPCR)评估了PTEN和miR-26a-5p的基因表达水平,Western印迹评估了PTEN、PI3K、p-PI3K、Akt和p-Akt的蛋白水平。结果显示,与模型组相比,步阳黄酒煎剂能促进脑缺血再灌注大鼠神经功能的恢复,缩小脑梗死体积,增加BrdU~+/NeuN~+神经元数量,上调miR-26a-5p的表达,调节PTEN/PI3K/Akt信号通路,促进神经元再生。这些作用在侧脑室注射 miR-26a-5p 激动剂后明显增强。研究结果证明,通过miR-26a-5p介导的PTEN/PI3K/Akt信号通路,步阳黄酒煎剂能促进脑缺血再灌注大鼠神经功能恢复,减少脑梗死体积,促进神经元再生。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
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581
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