Borneol attenuates inflammation and inhibits cardiac remodeling after myocardial infarction in mice via TRPM8
10.3969/j.issn.1000-4718.2024.00.010
- VernacularTitle:冰片通过TRPM8减轻小鼠心肌梗死后炎症反应并抑制心脏重构
- Author:
Yingrong HE
1
,
2
;
Tao HU
;
Wushuai WANG
;
Xi YANG
;
Qinghua DUAN
;
Xuan DU
;
Qiang WANG
Author Information
1. 西南医科大学临床医学院心血管内科,四川 泸州 646000
2. 西部战区总医院心血管内科,四川 成都 610083
- Keywords:
myocardial infarction;
cardiac remodeling;
borneol;
transient receptor potential cation channel subfamily M member 8;
inflammation
- From:
Chinese Journal of Pathophysiology
2024;40(3):456-464
- CountryChina
- Language:Chinese
-
Abstract:
AIM:To examine the effects of borneol on inflammation and myocardial remodeling after myocar-dial infarction(MI)in mice,and to investigate the underlying mechanisms.METHODS:Eight-week-old wild-type(WT)C57BL/6 mice and transient receptor potential cation channel subfamily M member 8(TRPM8)gene knockout(TRPM8-/-)mice were randomly divided into sham and MI groups,and were subsequently treated with normal saline(control group)or borneol(borneol group)via gavage.Survival curves were plotted for WT and TRPM8-/-mice with MI treated with or with-out borneol.After 28 d,cardiac function of the mice was assessed through echocardiography,and haemodynamic indexes were evaluated using a multi-channel physiological instrument.Infarct size,myocardial hypertrophy and interstitial fibro-sis were assessed via pathological staining.In addition,inflammatory response in the peri-infarct region was detected.RE-SULTS:The TRPM8 expression was up-regulated in the peri-infarct region of the mice with MI(P＜0.05),and borneol had no effect on TRPM8 expression(P＞0.05).Borneol increased the survival rate,reduced the infarct size,inhibited car-diac remodeling and improved cardiac function in WT mice with MI(P＜0.05 or P＜0.01).However,it did not affect the survival rate,infarct size,myocardial hypertrophy,myocardial fibrosis or cardiac function in TRPM8-/-mice(P＞0.05).Furthermore,borneol reduced inflammatory cell infiltration and the expression of inflammatory cytokines,tumor necrosis factor-α(TNF-α),interleukin-1β(IL-1β),IL-6 and monocyte chemotactic protein-1(MCP-1),in WT mice(P＜0.05 or P＜0.01)but not in TRPM8-/-mice(P＞0.05).CONCLUSION:Borneol attenuates inflammation,inhibits cardiac re-modeling and improves cardiac function in mice with MI via TRPM8.
