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.