通络清脑方治疗急性缺血性脑卒中的药理机制探讨网络药理学、分子对接和实验证据相结合的方法

Feng Li , Yilei Dong , Guangrui Wang , Zishan Huang , Wenting Song , Xiaoyu Zheng , Peng Zhang , Mingjiang Yao
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引用次数: 0

摘要

导言 通络活血方(TLQN)是一种中药专利注射剂,专门用于治疗急性缺血性中风(AIS)及其相关并发症。先前的研究表明,通络清脑汤在治疗缺血性脑水肿方面具有良好的潜力。本研究旨在通过生物信息学分析和确证实验,揭示TLQN治疗AIS的具体机制。方法采用高效液相色谱法分析TLQN的有效成分,引入网络药理学和分子对接法筛选治疗靶点和通路。结果TLQN中含有7种主要活性成分。网络药理学确定 IL-6 和 IL-1β 为主要靶点,PI3K-AKT 为关键通路。分子对接分析表明,TLQN 的成分与关键靶点具有很高的亲和力。TLQN 能明显减轻 AIS 引起的神经功能缺损、病理损伤和细胞凋亡。Western blotting结果表明,TLQN能激活PI3K-AKT信号通路,抑制促凋亡蛋白bax、Caspase-3和炎症因子IL-6、IL-1β的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring the pharmacological mechanism of Tongluo Qingnao formula in treating acute ischemic stroke: A combined approach of network pharmacology, molecular docking and experimental evidences

Exploring the pharmacological mechanism of Tongluo Qingnao formula in treating acute ischemic stroke: A combined approach of network pharmacology, molecular docking and experimental evidences

Introduction

Tongluo Qingnao (TLQN) Formula is a patent Traditional Chinese Medicine injection designed for the treatment of Acute Ischemic Stroke (AIS) and associated complications. Previous researches had shown promising potential of TLQN in treating ischemic brain edema. This study aimed to reveal specific mechanisms of TLQN in treating AIS by bioinformatics analysis and following confirmatory experiments.

Methods

HPLC was used to analyze the active ingredients of TLQN. Network Pharmacology and Molecular Docking were introduced to screen treatment targets and pathways. And then middle cerebral artery occlusion and reperfusion (MCAO/R) model was established in rats to verify the therapeutic effect of TLQN in neurological deficit score, cerebral infarction size, HE staining, TUNEL staining, and proteins expression related to inflammation, apoptosis and the PI3K-AKT signaling pathway.

Results

Seven main active ingredients were contained in TLQN. Network pharmacology identified IL-6 and IL-1β as the key targets, and PI3K-AKT as the critical pathway. Molecular Docking analysis indicated that the constituents of TLQN demonstrated a high affinity for crucial targets. TLQN could significantly reduce neurological deficits, pathological lesions and apoptosis caused by AIS. Western blotting results indicated that TLQN can activate the PI3K-AKT signaling pathway, inhibit the expression of pro-apoptotic proteins bax, Caspase-3 and inflammatory factors IL-6, IL-1β.

Discussion

TLQN has a therapeutic effect on AIS, and these results highlight the therapeutic effects of TLQN on AIS by activating PI3K-AKT signaling pathway to inhibit inflammation and apoptosis.
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