The dual role of the cystathionine γ-lyase/hydrogen sulfide pathway in CVB3-induced myocarditis in mice

被引:18
作者
Hua, Wang
Jiang, Jianbin
Rong, Xing
Wu, Rongzhou
Qiu, Huixian
Zhang, Yuanhai
Chen, Qi [1 ]
机构
[1] Second Affiliated Hosp, Dept Pediat Cardiol, Wenzhou 325027, Peoples R China
关键词
Hydrogen sulfide; Cystathionine gamma-lyase; Myocarditis; Coxsakievirus B3(CVB3); DL-proparglygylcine; ENDOGENOUS HYDROGEN-SULFIDE; PUNCTURE-INDUCED SEPSIS; COXSACKIEVIRUS B3 REPLICATION; CECAL LIGATION; NITRIC-OXIDE; ENDOTHELIAL-CELLS; KAPPA-B; H2S; INHIBITION; VASORELAXANT;
D O I
10.1016/j.bbrc.2009.08.064
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The present study found that serum H2S level, H2S production rate, CSE mRNA and CSE protein levels were increased in CVB3-induced myocarditis. DL-proparglygylcine (PAG), an irreversible CSE inhibitor, decreased the infected myocardium titers on postinfection day 4, while NaHS, a H2S donor, alleviated myocardial injury and necrosis, inflammatory cell infiltration and interstitial edema on postinfection day 10. These data reveal that the CSE/H2S pathway is upregulated in the heart in a murine model of CVB3-induced myocarditis and that inhibition of endogenous H2S is beneficial to treatment early in the disease while administration of exogenous H2S is protective to infected myocardium during the later stage. Published by Elsevier Inc.
引用
收藏
页码:595 / 600
页数:6
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