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Schisandra chinensis acidic polysaccharide partialy reverses acetaminophen-induced liver injury in mice

Authors :
Jinying Che
Shuo Yang
Zijing Qiao
He Li
Jinghui Sun
Wenyue Zhuang
Jianguang Chen
Chunmei Wang
Source :
Journal of Pharmacological Sciences, Vol 140, Iss 3, Pp 248-254 (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

Schisandra chinensis is a hepatoprotective herb that has been used for centuries in China. Polysaccharide is one of the major active components in S. chinensis, which has been reported to improve liver injuries induced by carbon tetrachloride, alcohol, or high-fat diet. In this study, we observed the effects and corresponding mechanisms of the secondary component of Schisandra polysaccharide (acidic polysaccharide, SCAP) on a murine model of severe acute liver injury induced by acetaminophen (APAP). SCAP significantly decreased the serum alanine aminotransferase (ALT), aspartate aminotransferas (AST), tumor necrosis factor-α (TNF-α), and interleukin-1β (IL-1β) levels, and was found to alleviate hepatic pathological alterations in the mouse model. Meanwhile, SCAP revealed a protective effects on the liver injury-related enzymes and factors, such as significantly diminished malondialdehyde (MDA) levels and glutathione (GSH) depletion, reduced ratio of B-cell lymphoma-2 (Bcl-2)-associated X protein (Bax)/Bcl-2, prohibited cleaved caspase-3 expression, and elevated the expression of p-AMPK, p-Akt, p-glycogen synthase kinase 3β (GSK 3β), nuclear factor erythroid 2–derived-like 2 (Nrf 2) and heme oxygenase-1 (HO-1) proteins in the liver tissues of the mouse model. In conclusion, we speculated that the protective activities of SCAP on the APAP-induced mouse model of acute liver injury might be related to its antioxidation, anti-inflammation and anti-apoptosis properties. Keywords: Schisandra chinensis, Polysaccharide, Hepatoprotection, Antioxidation

Subjects

Subjects :
Therapeutics. Pharmacology
RM1-950

Details

Language :
English
ISSN :
13478613
Volume :
140
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Journal of Pharmacological Sciences
Publication Type :
Academic Journal
Accession number :
edsdoj.734ed56e473e48a4a538d1c1e4531276
Document Type :
article
Full Text :
https://doi.org/10.1016/j.jphs.2019.07.008