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β-石竹烯通过作用于HMGB1/TLR4/NF-κB通路减轻小鼠局灶性脑缺血再灌注损伤

杨梅 安瑞娣 李明航 田晓翠 徐露 董志

中国免疫学杂志2017,Vol.33Issue(7):1009-1013,5.
中国免疫学杂志2017,Vol.33Issue(7):1009-1013,5.DOI:10.3969/j.issn.1000-484X.2017.07.011

β-石竹烯通过作用于HMGB1/TLR4/NF-κB通路减轻小鼠局灶性脑缺血再灌注损伤

β-caryophyllene mitigates cerebral ischemia reperfusion injury in mice by inhibiting HMGB1/TLR4/NF-κB pathway

杨梅 1安瑞娣 1李明航 1田晓翠 1徐露 1董志1

作者信息

  • 1. 重庆医科大学药学院 重庆市生物化学与分子药理重点实验室,重庆400016
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摘要

Abstract

Objective:investigate the effect of β-caryophyllene(BCP)on cerebral ischemia-reperfusion(CIR)injury in mice.Methods: Mice were subjected to CIR with or without BCP(62,124,248 mg/kg).At 24 h of reperfusion,ischemic degrees were determined according to neurologic dysfunction score and cerebral infarct volume.The protein expression of Toll-like receptor(TLR)4 was measured by Western blot.Nuclear factor κB(NF-κB)p65 were measured by immunohistochemistry and Western blot.IL-1β,tumor necrosis factor-α(TNF-α)and serum high-mobility group box 1(HMGB1)levels were measured by ELISA kit.Results: Compared to the CIR group,BCP(248 mg/kg)reduced the neurological score and cerebral infarct volume.BCP reduced neuronal death in mice brain subjected to cerebral I/R.In addition,BCP also inhibited the activation of NF-κB pathway and decreased increases in TLR4,HMGB1,TNF-α,IL-1β levels by CIR(P<0.01).Conclusion: BCP protects mice brain against CIR injury,its neuroprotective mechanisms may involves HMGB1/TLR4/NF-κB pathway.

关键词

β-石竹烯/缺血再灌注损伤/炎症/TLR4/HMGB1

Key words

β-caryophyllene/Ischemia-reperfusion injury/Inflammation/Toll-like receptor 4/High-mobility group box 1

分类

医药卫生

引用本文复制引用

杨梅,安瑞娣,李明航,田晓翠,徐露,董志..β-石竹烯通过作用于HMGB1/TLR4/NF-κB通路减轻小鼠局灶性脑缺血再灌注损伤[J].中国免疫学杂志,2017,33(7):1009-1013,5.

基金项目

本文为重庆市自然科学基金重点项目(KJ1600235, CSTC20 16jcyjA0258). (KJ1600235, CSTC20 16jcyjA0258)

中国免疫学杂志

OA北大核心CSCDCSTPCD

1000-484X

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