Luteolin inhibits CVB3 replication through inhibiting inflammation

J Asian Nat Prod Res. 2020 Aug;22(8):762-773. doi: 10.1080/10286020.2019.1642329. Epub 2019 Jul 19.

Abstract

Coxsackievirus B3 (CVB3) infection causes many inflammation-related diseases, such as viral myocarditis and aseptic meningitis. However, no vaccines or drugs have been approved for prevention or therapy of CVB3-induced diseases. In this study, luteolin (3,4,5,7-tetrahydroxyflavone) had been found that could dose-dependently reduce the production of viral progeny and synthesis of CVB3 RNA and protein. The luteolin-mediated inhibition of CVB3 was found to be mechanistically possible, at least in part, through depressing the phosphorylation of p38 MAPK and JNK MAPK, and inhibiting NF-κB nuclear translocation and subsequently attenuated the expression of inflammatory cytokines in CVB3-infected cells. Luteolin may be a potential agent or supplement against CVB3 infection by inhibiting inflammation.

Keywords: Coxsackievirus B3; antiviral activity; inflammation; luteolin.

MeSH terms

  • Animals
  • Enterovirus B, Human*
  • Inflammation
  • Luteolin*
  • Mice
  • Mice, Inbred BALB C
  • Molecular Structure
  • Virus Replication

Substances

  • Luteolin