Saponins from the roots of Platycodon grandiflorum ameliorate high fat diet-induced non-alcoholic steatohepatitis

[Display omitted] •CKS ameliorates HFD-induced hepatic fibrosis.•CKS inhibits HFD-induced pro-inflammatory cytokines and fibrotic markers.•The effect relies on the activation of antioxidant enzyme and fatty acid oxidation. Platycodon grandiflorum has been healthy effects due to its various nutritiou...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2017-02, Vol.86, p.205-212
Hauptverfasser: Choi, Jae Ho, Jin, Sun Woo, Choi, Chul Yung, Kim, Hyung Gyun, Kim, Se Jong, Lee, Hyun Sun, Chung, Young Chul, Kim, Eun Ju, Lee, Young Chun, Jeong, Hye Gwang
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Sprache:eng
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Zusammenfassung:[Display omitted] •CKS ameliorates HFD-induced hepatic fibrosis.•CKS inhibits HFD-induced pro-inflammatory cytokines and fibrotic markers.•The effect relies on the activation of antioxidant enzyme and fatty acid oxidation. Platycodon grandiflorum has been healthy effects due to its various nutritious compounds and is considered as a functional food. Platycodon grandiflorum root-derived saponins (CKS) have been reported to show a variety of effects including anti-inflammatory and anti-oxidative activity. Although CKS have been studied on various bioactivities, the inhibitory effect of CKS on non-alcoholic steatohepatitis (NASH) is not examined. In this study, the inhibitory effects on HFD-induced NASH by CKS were determined. CKS suppressed HFD-induced hepatic lipid peroxidation level, collagen deposition, pro-fibrogenic and pro-inflammatory cytokines expression. CKS treatment suppressed HFD-induced COX-2 expression via inhibition of NF-κB p65 nuclear translocation and IκBα degradation. CKS treatment restored HFD-reduced Nrf2-mediated antioxidant enzymes expression. Furthermore, CKS treatment reinstated HFD-reduced peroxisomal proliferator-activated receptor alpha (PPARα)-regulated acyl-coA oxidase and carnitine-palmitoyl-coA transferase-1 expression. These findings suggest that CKS reduces HFD-induced NASH by up-regulation of Nrf2-mediated anti-oxidant enzymes and PPARα-regulated fatty acid oxidation.
ISSN:0753-3322
1950-6007
DOI:10.1016/j.biopha.2016.11.107