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. 2017 Aug 18;26(4):1071-1076.
doi: 10.1007/s10068-017-0170-7. eCollection 2017.

Antioxidant and hepatoprotective activity of kaempferol 3- O-β-d- (2,6-di- O-α-l-rhamnopyranosyl)galactopyronoside against carbon tetrachloride-induced liver injury in mice

Affiliations

Antioxidant and hepatoprotective activity of kaempferol 3- O-β-d- (2,6-di- O-α-l-rhamnopyranosyl)galactopyronoside against carbon tetrachloride-induced liver injury in mice

Yanqing Zang et al. Food Sci Biotechnol. .

Abstract

This study aims to investigate the antioxidant and hepatoprotective effects of kaempferol 3-O-β-d- (2,6-di-O-α-l-rhamnopyranosyl)galactopyronoside (KG) isolated from unripe soybean leaves. Carbon tetrachloride (CCl4)-induced hepatotoxic ddY mice were used in the study. The mice were divided into three groups, namely the control group, the CCl4 group (CCl4, CCl4 injected), and the KG group (KG, CCl4 injected with KG administration). Hepatic injury markers of serum and liver were analyzed. The results show that serum ALT, AST activities, hepatic glutathione, superoxide dismutase, catalase, and glutathione peroxidase activities were normalized in mice pretreated with KG. Furthermore, the liver thiobarbituric acid reactive substances levels were found to be improved by pretreatment with KG, indicating that KG is available to alleviate liver injury, this may be due to its antioxidant properties. This study suggests that unripe soy leaves could be used as functional food materials.

Keywords: Antioxidant activity; CCl4; Hepatotoxicity; Kaempferol 3-O-β-d- (2,6-di-O-α-l-rhamnopyranosyl)galactopyronoside; Mice.

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Conflict of interest statement

Compliance with ethical standardsThe authors declare no conflict of interest.

Figures

Fig. 1
Fig. 1
HPLC chromatograms and chemical structure of kaempferol 3-O-β-d- (2,6-di-O-α-l-rhamnopyranosyl)galactopyronoside (KG) isolated from unripe soybean (Jindai) leaves
Fig. 2
Fig. 2
Effects of KG on serum ALT (A) and AST (B) activities. Each value is mean ± SEM; n = 7 for each group. Values without a common letter differ significantly (p < 0.05). CON: control-group mice; CCl4: CCl4-injected-group mice; KG: CCl4-injected-group mice with KG administration
Fig. 3
Fig. 3
Effects of KG on liver GSH (A) and GSSG (B) levels. Each value is mean ± SEM; n = 7 for each group. Values without a common letter differ significantly (p < 0.05). CON: control-group mice; CCl4: CCl4-injected-group mice; KG: CCl4-injected-group mice with KG administration
Fig. 4
Fig. 4
Effects of KG on liver SOD (A), GSH-Px (B) and CAT (C) activities. Each value is mean ± SEM; n = 7 for each group. Values without a common letter differ significantly (p < 0.05). CON: control-group mice; CCl4: CCl4-injected-group mice; KG: CCl4-injected-group mice with KG administration
Fig. 5
Fig. 5
Effect of KG on liver TBARS level. Each value is mean ± SEM; n = 7 for each group. Values without a common letter differ significantly (p < 0.05). CON: control-group mice; CCl4: CCl4-injected-group mice; KG: CCl4-injected-group mice with KG administration

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