Nox4-dependent ROS production is involved in CVB3-induced myocardial apoptosis

Biochem Biophys Res Commun. 2018 Sep 10;503(3):1641-1644. doi: 10.1016/j.bbrc.2018.07.093. Epub 2018 Jul 23.

Abstract

Viral myocarditis is a cardiovascular disease that seriously affects human health. Its mechanism is not clear. Coxsackievirus B3 (CVB3) is a member of the picornavirus family and is the leading cause of viral myocarditis. Our group tested the genes in a mouse model of CVB3 virus infection and confirmed that the NADPH oxidase gene had a high expression trend in the acute phase of infection. Whether Nox4, the homologue of NADPH oxidase, participates in the process of viral myocarditis has not been reported. In this study, we found increased expression of Nox4 in viral myocarditis in vivo and in vitro. DPI is a non-specific inhibitor of Nox4 that improved CVB3-induced myocarditis after injection in vivo. DPI also inhibited intracellular ROS release and apoptosis in vitro. Our data indicated that Nox4-dependent ROS production was involved in CVB3-induced myocardial apoptosis.

Keywords: Apoptosis; CVB(3); Nox4; ROS; Viral myocarditis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • Enterovirus B, Human / metabolism*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Myocytes, Cardiac / metabolism*
  • Myocytes, Cardiac / pathology*
  • NADPH Oxidase 4 / metabolism*
  • Reactive Oxygen Species / metabolism*

Substances

  • Reactive Oxygen Species
  • NADPH Oxidase 4
  • Nox4 protein, mouse