β-caryophyllene mitigates cerebral ischemia reperfusion injury in mice by inhibiting HMGB1/TLR4/NF-κB pathway
10.3969/j.issn.1000-484X.2017.07.011
- VernacularTitle: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
- Author:
Mei YANG
;
Ruidi AN
;
Minghang LI
;
Xiaocui TIAN
;
Lu XU
;
Zhi DONG
- Keywords:
β-caryophyllene;
Ischemia-reperfusion injury;
Inflammation;
Toll-like receptor 4;
High-mobility group box 1
- From:
Chinese Journal of Immunology
2017;33(7):1009-1013
- CountryChina
- Language:Chinese
-
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.