Abstract
The increased expression and cross-linking activity of tissue transglutaminase (tTG) have been demonstrated in acute liver injury and fibrosis. We focused on the molecular mechanisms that contribute to ethanol-induced tTG expression and investigated the efficacy of propolis components in preventing both the tTG expression in vitro and fibrogenesis in vivo. We demonstrate herein that both ERK1/2 and PI3K/Akt pathways can regulate the effects of ethanol on NF-κB-dependent transcription and these signaling pathways may be involved in activation of ethanol-mediated tTG expression. We also found that administration of pinocembrin (PIN), one of the major components of propolis, inhibited tTG activation and significantly prevented the development of thioacetamide (TAA)-induced liver cirrhosis. The present study suggests that tTG may be an important member of the cascade of factors necessary for ethanol-induced liver fibrogenesis and PIN could serve as an anti-fibrogenic agent.
Original language | English |
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Pages (from-to) | 148-157 |
Number of pages | 10 |
Journal | Toxicology |
Volume | 246 |
Issue number | 2-3 |
DOIs | |
Publication status | Published - Apr 18 2008 |
Keywords
- Ethanol
- Fibrogenesis
- NF-κB
- Propolis
- Tissue transglutaminase
ASJC Scopus subject areas
- Toxicology