Curcumol alleviates cardiac and cerebral injury caused by encephalomyocarditis virus (EMCV) in Kunming mice via suppressing NF-κB/NLRP3 inflammasome pathway.

INTRODUCTION

Encephalomyocarditis virus (EMCV), a highly significant member of the picornaviridae family, infects a broad range of mammalian hosts and causes severe pathological consequences like encephalitis, myocarditis, and neurologic diseases, etc. In our previous research, curcumol demonstrated a significant reduction in EMCV replication in vitro. However, its antiviral effect in vivo needs to be elucidated.

METHODS

In this study, the mechanism of curcumol against EMCV replication was demonstrated in vivo by establishing an EMCV (100 TCID50/20 g) infected mice model. At day 3 post EMCV infection, drug treatment groups were continuously treated with curcumol for 5 days.

RESULTS

The viral load and expression of interleukins such as IL-1β, IL-6, and TNF-α mRNA levels were significantly decreased in the heart and brain tissues at day 9 of EMCV infection (5 days of curcumol treatment), detected by qPCR. Moreover, Western blot analysis revealed that curcumol considerably elevated the protein levels of IκB and P65, while significantly reducing the levels of P-IκB, P-P65, NLRP3 inflammasome, caspase 1, and IL-1β in cardiac and cerebral tissues.

DISCUSSION: Conclusively, these results revealed that curcumol inhibits the NF-κB/NLRP3 inflammasome pathway and thus alleviates heart and brain damage induced by EMCV infection in Kunming mice. The present findings provide new insights into the therapeutic potential of curcumol in addressing EMCV-induced pathological conditions.