Journal of cardiovascular translational research · 2015
Panax Notoginseng Saponins Ameliorates Coxsackievirus B3-Induced Myocarditis by Activating the Cystathionine-γ-Lyase/Hydrogen Sulfide Pathway.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Pan Lulu, Zhang Yuanhai, Lu Jiacheng, Geng Zhimin, Jia Lianhong, Rong Xing, Wang Zhenquan, Zhao Qifeng, Wu Rongzhou, Chu Maoping, Zhang Chunxiang
Аннотация
This study is to determine the therapeutic effects of Panax notoginseng saponins (PNSs) on coxsackievirus B3 (CVB3)-induced myocarditis, and whether cystathionine-γ-lyase (CSE)/hydrogen sulfide (H2S) pathway is involved. Mouse model of myocarditis was induced by CVB3 infection, and the mice were subjected to vehicle (saline) or drug treatments (sodium bisulfide (NaHS), propargylglycine (PAG), or PNSs). The results showed that there were inflammatory cell infiltrations, interstitial edemas, and elevated inflammatory cytokines, in CVB3-induced myocarditis. PAG administration increased, whereas NaHS treatment decreased the severity of the myocarditis. PNS treatment dramatically alleviated these myocardial injuries and decreased the viral messenger RNA (mRNA) expression by the enhanced expression of CSE/H2S pathway. Moreover, the therapeutic effects of PNSs on myocarditis were stronger than those of NaHS. Finally, the effect of PNSs on CSE/H2S pathway and cardiac cell protection were verified in cultured cardiac cells. PNSs may be a promising medication for viral myocarditis therapy.
Предметные рубрики MeSH
Analysis of VarianceAnimalsBiomarkersBlotting, WesternCoxsackievirus InfectionsCystathionine gamma-LyaseDisease Models, AnimalEnterovirus B, HumanEnzyme-Linked Immunosorbent AssayHumansHydrogen SulfideMaleMiceMice, Inbred BALB CMyocarditisPanax notoginsengPhytotherapyPlant PreparationsRNA, Small InterferingRandom AllocationReal-Time Polymerase Chain ReactionSaponinsSignal Transduction