Hepatoprotective effect of pyrroloquinoline quinone against alcoholic liver injury through activating Nrf2-mediated antioxidant and inhibiting TLR4-mediated inflammation responses. (May 2020)

• Record Type: Journal Article
• Authors: Jiang, Xiaoxia; Zhou, Yafeng; Zhang, Yun; Tian, Diying; Jiang, Su; Tang, Yunping
• Is Part Of: Process biochemistry. Volume 92(2020)
• Page Start: 303
• Page End: 312
• Publication Date: 2020-05
• Subjects: Pyrroloquinoline quinone -- Alcoholic liver injury -- Oxidative stress -- Nrf2 signal pathway -- NF-κB signal pathway; Biochemical engineering -- Periodicals; Biotechnology -- Periodicals; Biochemistry -- periodicals; Biotechnology -- periodicals; Chemical Engineering -- periodicals; Génie biochimique -- Périodiques; Biotechnologie -- Périodiques; Biochemical engineering; Biotechnology; Periodicals; 660.63
• DOI: 10.1016/j.procbio.2020.01.023
• Languages: English
• ISSNs: 1359-5113

Abstract

Graphical abstract: Highlights: PQQ alleviates acute alcoholic liver injury in mice. PQQ against acute alcoholic liver injury by activating Nrf2-mediated signaling in vivo . PQQ against acute alcoholic liver injury by inhibiting TLR4/NF-κB signaling in vivo . Abstract: The present study was aimed at investigating the hepatoprotective effect of pyrroloquinoline quinone (PQQ) against acute alcoholic liver injury in mice. Acute alcoholic liver injury model was established in mice, and they were administrated with PQQ to investigate its hepatoprotective effect. Our results shows that PQQ can significantly ameliorate acute alcoholic liver injury by decreasing the hepatic marker enzymes, including serum alanine transaminase (ALT) and aspartate transaminase (AST), and increasing the levels of alcohol dehydrogenase (ADH), aldehyde dehydrogenase (ALDH), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) in the liver. And PQQ can also significantly reduce the content of hepatic triglyceride (TG) and malondialdehyde (MDA). Moreover, PQQ attenuated alcohol-induced oxidative damage by activating NF-E2-related factor 2 (Nrf2)-mediated signaling pathway, and inhibiting Toll-like receptor 4 (TLR4)-mediated nuclear factor-kappa B (NF-κB) signaling pathway. Our findings have elucidated the liver protection mechanism of PQQ, which would encourage the further exploitation of PQQ as a hepatoprotective functional food.