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首页> 外文期刊>Circulation research: a journal of the American Heart Association >Bosentan enhances viral load via endothelin-1 receptor type-A-mediated p38 mitogen-activated protein kinase activation while improving cardiac function during coxsackievirus-induced myocarditis.
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Bosentan enhances viral load via endothelin-1 receptor type-A-mediated p38 mitogen-activated protein kinase activation while improving cardiac function during coxsackievirus-induced myocarditis.

机译:波生坦通过内皮素-1受体A型介导的p38丝裂原活化的蛋白激酶活化增强病毒载量,同时改善柯萨奇病毒诱发的心肌炎期间的心脏功能。

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摘要

Reduced cardiac output is one of the consequences of myocarditis. Bosentan, an endothelin-1 receptor (ET1R) antagonist, could be useful to reduce cardiac afterload, preserving cardiac output. In this study, we investigated the potential therapeutic use of bosentan in an animal model of viral myocarditis. Using a mouse model of coxsackievirus B3 (CVB3)-induced myocarditis, we demonstrated preserved ejection fraction (EF) and fractional shortening (FS) by treatment with bosentan (68+/-5.8% EF and 40+/-3.7% FS for treated versus 48+/-2.2% EF and 25+/-2.6% FS for controls; P=0.028). However, bosentan enhanced cardiac viral load (10.4+/-6.7% in the bosentan group versus 5.0+/-5.5% in control group; P=0.02), likely through enhancement of p38 mitogen-activated protein kinase (MAPK) phosphorylation (0.77+/-0.40% ATF2 activation in the bosentan group versus 0.03+/-0.02% in controls; P=0.0002), mediated by endothelin receptor type-A. We further demonstrate that a water soluble inhibitor of p38 MAPK, SB203580 HCl, is a potent inhibitor of virus replication in the heart (0.28% antisense viral genome stained area for 3 mg/kg dose versus 2.9% stained area for controls; P=0.01), attenuates CVB3-induced myocardial damage (blinded cardiac histopathologic scores of 1.8+/-1.6 and 2.05+/-1.2 for the 3 mg/kg and 10 mg/kg doses, respectively, versus 3.25+/-1.2 for the controls), and preserves cardiac function (69+/-3.5% EF for 3 mg/kg dose and 71+/-6.7% EF for 10 mg/kg dose versus 60+/-1.5% EF control; P=0.038 and P=0.045, as compared to control, respectively). Bosentan, a prescribed vasodilator, improves cardiac function but enhances viral load and myocarditis severity through ETRA mediated p38 MAPK activation; p38 MAPK is a desirable antiviral target. Caution must be exercised during treatment of suspected infectious myocarditis with supportive vasoactive remedies.
机译:心排血量减少是心肌炎的后果之一。 Bosentan是一种内皮素1受体(ET1R)拮抗剂,可用于减少心脏后负荷,并保持心输出量。在这项研究中,我们调查了波生坦在病毒性心肌炎动物模型中的潜在治疗用途。使用柯萨奇病毒B3(CVB3)诱导的心肌炎的小鼠模型,我们证明了通过波生坦(68 +/- 5.8%EF和40 +/- 3.7%FS)的治疗,保留了射血分数(EF)和缩短分数(FS)对照则为48 +/- 2.2%EF和25 +/- 2.6%FS; P = 0.028)。然而,波生坦增强了心脏病毒负荷(波生坦组为10.4 +/- 6.7%,对照组为5.0 +/- 5.5%; P = 0.02),可能是通过增强p38丝裂原活化的蛋白激酶(MAPK)磷酸化而实现的(0.77波生坦组中+/- 0.40%的ATF2活化,而对照组为0.03 +/- 0.02%; P = 0.0002),由A型内皮素介导。我们进一步证明,p38 MAPK的水溶性抑制剂SB203580 HCl是心脏中病毒复制的有效抑制剂(0.2 mg反义病毒基因组染色区域,3 mg / kg剂量,而对照组为2.9%染色区域; P = 0.01 ),可减轻CVB3引起的心肌损伤(3 mg / kg和10 mg / kg剂量的盲人心脏病理学评分分别为1.8 +/- 1.6和2.05 +/- 1.2,而对照组为3.25 +/- 1.2) ,并保持心脏功能(3 mg / kg剂量时为69 +/- 3.5%EF,10 mg / kg剂量时为71 +/- 6.7%EF,而EF对照为60 +/- 1.5%; P = 0.038和P = 0.045 ,分别与对照相比)。 Bosentan是一种处方药,可通过ETRA介导的p38 MAPK激活改善心脏功能,但可增加病毒载量和心肌炎的严重程度; p38 MAPK是理想的抗病毒靶标。在治疗疑似感染性心肌炎的过程中,必须采取支持性血管活性药物的措施。

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