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基于Toll样受体信号通路探讨脑心通胶囊“脑心同治”机制

[Exploration of mechanism of "simultaneous treatment of brain and heart" of Naoxintong Capsules based on Toll-like receptor signaling pathway].

作者信息

Li Qian-Nan, Shang Jin-Feng, Jiang Ting-Yue, Bi Lei, Jiao Jia-Kang, Lu Ying-Hui, Song Qi, Lizha Shabuer-Jiang, Liu Xin

机构信息

School of Chinese Materia Medica, Beijing University of Chinese Medicine Beijing 102488, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2022 Aug;47(15):4110-4118. doi: 10.19540/j.cnki.cjcmm.20220211.401.

Abstract

This study aims to explore the mechanism of "simultaneous treatment of the brain and the heart" of Naoxintong Capsules(NXT) under cerebral ischemia based on Toll-like receptor(TLR) signaling pathway.Male SD rats were randomized into sham operation group, model group, NXT group, and positive drug group.Middle cerebral artery occlusion(MCAO) model rats were used in model group, NXT group, and positive drug group, respectively.Neurological function was scored with the Bederson scale, and brain infarct rate was measured by 2,3,5-triphenyltetrazolium chloride(TTC) staining.Brain edema was detected with wet-dry weight method.Hematoxylin-eosin(HE) staining and TdT-mediated dUTP nick-end labeling(TUNEL) staining were used to observe and count apoptotic cardiocytes.In addition, serum myocardial enzymes were measured.The expression of 8 TLR signaling pathway-related proteins interferon-α(IFN-α), interferon regulatory factor-3(IRF3), interferon regulatory factor-7(IRF7), TLR2, TLR4, TLR7, TLR9, and tumor necrosis factor-α(TNF-α) in the cerebral cortex and heart of rats was detected by Western blot. Brain infarct rate, neurological function score, and brain water content in NXT group decreased significantly compared with those in the model group. At the same time, the reduction in apoptosis rate of cardiocytes and the content of serum aspartate aminotransferase(AST), alanine aminotransferase(ALT), creatine kinase(CK), and lactate dehydrogenase(LDH) were decreased in the NXT group.Systems pharmacological results and previous research showed that TLR signaling pathway played an important role in immune inflammatory response.The study of TLR signaling pathway and related proteins is helpful to elucidate the mechanism of "simultaneous treatment of the brain and the heart". Western blot results showed that NXT significantly inhibited the expression of IRF3, IRF7, TLR2, TLR7, and TNF-α in cerebral cortex and heart under cerebral ischemia.Cerebral ischemia influences cardiac functions, and TLR signaling pathway is one of the pathways for "simultaneous treatment of the brain and the heart" of NXT.

摘要

本研究旨在基于Toll样受体(TLR)信号通路探讨脑心通胶囊(NXT)在脑缺血状态下“脑心同治”的机制。将雄性SD大鼠随机分为假手术组、模型组、NXT组和阳性药物组。模型组、NXT组和阳性药物组分别采用大脑中动脉闭塞(MCAO)模型大鼠。采用Bederson评分法对神经功能进行评分,通过2,3,5-三苯基四氮唑氯化物(TTC)染色测量脑梗死率。采用干湿重法检测脑水肿。采用苏木精-伊红(HE)染色和TdT介导的dUTP缺口末端标记(TUNEL)染色观察并计数凋亡心肌细胞。此外,检测血清心肌酶。采用蛋白质印迹法检测大鼠大脑皮质和心脏中8种TLR信号通路相关蛋白,即干扰素-α(IFN-α)、干扰素调节因子-3(IRF3)、干扰素调节因子-7(IRF7)、TLR2、TLR4、TLR7、TLR9和肿瘤坏死因子-α(TNF-α)的表达。与模型组相比,NXT组脑梗死率、神经功能评分和脑含水量均显著降低。同时,NXT组心肌细胞凋亡率降低,血清天冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)、肌酸激酶(CK)和乳酸脱氢酶(LDH)含量降低。系统药理学结果和既往研究表明,TLR信号通路在免疫炎症反应中起重要作用。对TLR信号通路及相关蛋白的研究有助于阐明“脑心同治”的机制。蛋白质印迹法结果显示,脑缺血时NXT可显著抑制大脑皮质和心脏中IRF3、IRF7、TLR2、TLR7和TNF-α的表达。脑缺血影响心脏功能,TLR信号通路是脑心通胶囊“脑心同治”的途径之一。

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