2008•Journal of the Science of Food and AgricultureRequires access

The protective effects of garlic oil on acute ethanol‐induced oxidative stress in the liver of mice

Tao Zeng, Cuili Zhang, Guang-bing Pan, Sheng Zhao, Dandan Dou, Xing Xin, Keqin Xie

Open publisher page 17 citations

Abstract

Abstract BACKGROUND: Alcoholic liver disease is so serious that no effective therapies have been developed up to now. This study was conducted to elucidate the effects of garlic oil (GO) on acute ethanol‐induced liver injury. Male Kun‐Ming mice were orally administered GO (50, 100 or 200 mg kg−1) for 30 days and then ethanol (4.8 g kg−1). At 16 h after ethanol treatment the mice were sacrificed. Subsequent serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) and triglyceride (TG) levels, hepatic malondialdehyde (MDA) and glutathione (GSH) levels and antioxidant enzyme activities were measured. Histopathological examination of mouse liver sections was performed by Sudan III staining. RESULTS: GO pretreatment significantly inhibited acute ethanol‐induced increase in ALT, AST, TG and MDA and decrease in GSH in a dose‐dependent manner. In the three GO groups the level of GSH increased by 10.3%, 15.8% (P < 0.05) and 25.5% (P < 0.01) respectively compared with that in the ethanol group. The activities of superoxide dismutase, catalase and glutathione reductase were increased markedly in the 200 mg kg−1 GO group (P < 0.01). Histopathological examination showed fewer fat droplets in liver sections of GO‐pretreated mice. CONCLUSION: GO may have protective effects against acute ethanol‐induced liver injury through restoration of the GSH level and enhancement of the activities of antioxidant enzymes. Copyright © 2008 Society of Chemical Industry

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What this paper is about

Abstract BACKGROUND: Alcoholic liver disease is so serious that no effective therapies have been developed up to now. This study was conducted to elucidate the effects of garlic oil (GO) on acute ethanol‐induced liver injury. Male Kun‐Ming mice were orally administered GO (50, 100 or 200 mg kg−1) for 30 days and then ethanol (4.8 g kg−1). At 16 h after ethanol treatment the mice were sacrificed. Subsequent serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) and triglyceride (TG) levels, hepatic malondialdehyde (MDA) and glutathione (GSH) levels and antioxidant enzyme activities were measured. Histopathological examination of mouse liver sections was performed by Sudan III staining. RESULTS: GO pretreatment significantly inhibited acute ethanol‐induced increase in ALT, AST, TG and MDA and decrease in GSH in a dose‐dependent manner. In the three GO groups the level of GSH increased by 10.3%, 15.8% (P < 0.05) and 25.5% (P < 0.01) respectively compared with that in the ethanol group. The activities of superoxide dismutase, catalase and glutathione reductase were increased markedly in the 200 mg kg−1 GO group (P < 0.01). Histopathological examination showed fewer fat droplets in liver sections of GO‐pretreated mice. CONCLUSION: GO may have protective effects against acute ethanol‐induced liver injury through restoration of the GSH level and enhancement of the activities of antioxidant enzymes. Copyright © 2008 Society of Chemical Industry

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Available abstract

Abstract BACKGROUND: Alcoholic liver disease is so serious that no effective therapies have been developed up to now. This study was conducted to elucidate the effects of garlic oil (GO) on acute ethanol‐induced liver injury. Male Kun‐Ming mice were orally administered GO (50, 100 or 200 mg kg−1) for 30 days and then ethanol (4.8 g kg−1). At 16 h after ethanol treatment the mice were sacrificed. Subsequent serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) and triglyceride (TG) levels, hepatic malondialdehyde (MDA) and glutathione (GSH) levels and antioxidant enzyme activities were measured. Histopathological examination of mouse liver sections was performed by Sudan III staining. RESULTS: GO pretreatment significantly inhibited acute ethanol‐induced increase in ALT, AST, TG and MDA and decrease in GSH in a dose‐dependent manner. In the three GO groups the level of GSH increased by 10.3%, 15.8% (P < 0.05) and 25.5% (P < 0.01) respectively compared with that in the ethanol group. The activities of superoxide dismutase, catalase and glutathione reductase were increased markedly in the 200 mg kg−1 GO group (P < 0.01). Histopathological examination showed fewer fat droplets in liver sections of GO‐pretreated mice. CONCLUSION: GO may have protective effects against acute ethanol‐induced liver injury through restoration of the GSH level and enhancement of the activities of antioxidant enzymes. Copyright © 2008 Society of Chemical Industry

Key concepts: Malondialdehyde, Glutathione, Glutathione reductase, Antioxidant, Oxidative stress, Superoxide dismutase, Glutathione peroxidase, Chemistry

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