No abstract

Hepatitis represents a ubiquitous human health problem but effective therapies with limited side effects are still lacking. In this study, we investigated the effect and mechanism of TP-58, a novel thienopyridine derivative, on a murine fulminant hepatitis model induced by concanavalin A (ConA). We found TP-58 markedly alleviated ConA-caused liver injury and increased survival ratio of mice injected with a lethal dose of ConA. Oral administration of TP-58 significantly alleviated ConA-caused liver injury in mice by the reduction of serum aminotransferases and liver necrosis.The analysis of proinflammatory cytokines showed that TP-58 decreased both hepatic mRNA expressions and serum protein levels of TNF-α and IL-6. And the result from LPS-stimulated RAW 264.7 cells showed TP-58 suppressed the production of TNF-α, IL-6, and Nitro Oxide (NO) in the supernatant of LPS-stimulated RAW 264.7 cells. The study of activation of nuclear factor-ĸB (NF-ĸB) by electrophoretic mobility shift assay (EMSA) showed that TP-58 inhibited the activation of NF-ĸB both in vivo and in vitro. The inhibitory effect was also accompanied by a parallel reduction of IĸB phosphorylation. These results indicate that TP-58 protects against liver injury by inhibition of the NF-ĸB-mediated inflammation and suggest a potential role of TP-58 against acute liver injury and other inflammatory diseases.