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Iridoid Glycosides Fraction Isolated from Veronica ciliata Fisch. Protects against Acetaminophen-Induced Liver Injury in Mice.
Evidence-based Complementary & Alternative Medicine (eCAM)
Short Title: Evidence-based Complementary & Alternative Medicine (eCAM)
Format: Journal Article
Publication Date: 2017/02/13/
Pages: 1 - 11
Sources ID: 93816
Notes: Accession Number: 121255431; Source Information: 2/13/2017, Vol. 2017, p1; Subject Term: THERAPEUTIC use of antioxidants; Subject Term: PLANT extracts -- Therapeutic use; Subject Term: GLYCOSIDES -- Therapeutic use; Subject Term: ACETAMINOPHEN; Subject Term: ANIMAL experimentation; Subject Term: ASPARTATE aminotransferase; Subject Term: CHROMATOGRAPHIC analysis; Subject Term: GLUTATHIONE; Subject Term: GLYCOSIDES; Subject Term: LIVER diseases; Subject Term: TIBETAN medicine; Subject Term: MICE; Subject Term: TUMOR necrosis factor; Subject Term: MALONDIALDEHYDE; Subject Term: ALANINE aminotransferase; Subject Term: FREE radical scavengers; Subject Term: IN vitro studies; Subject Term: IN vivo studies; Subject Term: ; Number of Pages: 11p; ; Illustrations: 1 Color Photograph, 1 Chart, 6 Graphs; ; Document Type: Article;
Visibility: Public (group default)
Abstract: (Show)
Veronica ciliata Fisch. has traditionally been used in Tibetan medicine for the treatment of hepatitis, cholecystitis, rheumatism, and urticaria. We analyzed the chemical composition of the iridoid glycosides fraction (IGF) isolated from V. ciliata and evaluated the antioxidant and hepatoprotective properties. The IGF was separated by high-speed countercurrent chromatography (HSCCC) and the main compounds were identified by ultra-performance liquid chromatography coupled to a photodiode array. We determined the in vitro antioxidant ability of the IGF through radical scavenging assays and assessed the in vivo hepatoprotective potential in an acetaminophen- (APAP-) induced acute liver injury murine model. The IGF was separated by HSCCC and three major iridoid glycosides (verproside, catalposide, and amphicoside) were identified as potent antioxidants and hepatoprotective compounds. Treatment with the IGF significantly suppressed the APAP-induced elevation in serum alanine aminotransferase, aspartate aminotransferase, and tumor necrosis factor-alpha (TNF-α); improved serum total antioxidant capacity; decreased malondialdehyde formation; elevated superoxide dismutase and glutathione activity; and decreased expression of proinflammatory factors (TNF-α, nuclear factor kappa B) in the liver. Finally, we examined the histopathology of resected livers for evidence of hepatoprotection. The protection conferred by the IGF may be related to the reinforcement of antioxidant defense systems. [ABSTRACT FROM AUTHOR]