Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/73419

TítuloHepatoprotective effect of Phellinus linteus mycelia polysaccharide (PL-N1) against acetaminophen-induced liver injury in mouse
Autor(es)Chen, Chen
Liu, Xiang
Qi, Shanshan
Dias, Alberto Carlos Pires
Yan, Jingkun
Zhang, Xiaoying
Palavras-chaveAnimals
Chemical and Drug Induced Liver Injury
Cytokines
Cytoprotection
Female
Fungal Polysaccharides
Hep G2 Cells
Humans
Liver
Mice
Mycelium
Oxidative Stress
Phellinus
Rats, Sprague-Dawley
Phellinus linteus
Polysaccharide
Acetaminophen
Drug-induced liver injury
Cytochrome P450 2E1
Data2020
EditoraElsevier 1
RevistaInternational Journal of Biological Macromolecules
CitaçãoChen, C., Liu, X., Qi, S., C.P. Dias, A., Yan, J., & Zhang, X. (2020). Hepatoprotective effect of Phellinus linteus mycelia polysaccharide (PL-N1) against acetaminophen-induced liver injury in mouse. International Journal of Biological Macromolecules, 154, 1276-1284. doi: https://doi.org/10.1016/j.ijbiomac.2019.11.002
Resumo(s)Edible and medicinal fungi are one of the major sources for extraction and identification of polysaccharides, which are important biological response modifiers with notable antitumor, hepatoprotective effect and other pharmacological activities. This study aimed to evaluate the hepatoprotective effect of isolated Phellinus linteus polysaccharide (PL-N1) against acetaminophen (APAP) induced liver injury in mice. Mice were treated intragastrical with PL-N1 (10, 50 and 100 mg/kg) and APAP (300 mg/kg) injection. APAP alone caused increased serum aminotransferase levels and changes in hepatic histopathology, promoted oxidative stress by increasing lipid peroxidation and decreasing anti-oxidant enzyme activities, leading to hepatocellular necrosis and reduced liver function. PL-N1 decreased cytochrome P450 2E1 (CYP2E1) expression and hepatic release of cytokines to enhance the level of phase II enzymes. Also, PL-N1 obviously accelerates the metabolism of APAP in the rat model. Molecular docking analysis revealed the α-d-glucopyranosyl exhibit maximum interaction (-8.099) against CYP2E1 as comparably less than standard drug silibinin (-13.767). PL-N1 could be a promising natural substance for ameliorating acute APAP-induced oxidative stress and hepatic injury.
TipoArtigo
URIhttps://hdl.handle.net/1822/73419
DOI10.1016/j.ijbiomac.2019.11.002
ISSN0141-8130
Versão da editorahttps://www.sciencedirect.com/science/article/pii/S0141813019347968
Arbitragem científicayes
AcessoAcesso restrito UMinho
Aparece nas coleções:CBMA - Artigos/Papers
DBio - Artigos/Papers

Ficheiros deste registo:
Ficheiro Descrição TamanhoFormato 
1-s2.0-S0141813019347968-main.pdf
Acesso restrito!
1,91 MBAdobe PDFVer/Abrir

Partilhe no FacebookPartilhe no TwitterPartilhe no DeliciousPartilhe no LinkedInPartilhe no DiggAdicionar ao Google BookmarksPartilhe no MySpacePartilhe no Orkut
Exporte no formato BibTex mendeley Exporte no formato Endnote Adicione ao seu ORCID