BackgroundIt is a widespread belief in Asian countries that mung bean soup (MBS) may afford a protective effect against heat stress. Lack of evidence supports MBS conferring a benefit in addition to water.ResultsHere we show that vitexin and isovitexin are the major antioxidant components in mungbean (more than 96% of them existing in the bean seed coat), and both of them could be absorbed via gavage into rat plasma. In the plasma of rats fed with mungbean coat extract before or after exposure to heat stress, the levels of malonaldehyde and activities of lactate dehydrogenase and nitric oxide synthase were remarkably reduced; the levels of total antioxidant capacity and glutathione (a quantitative assessment of oxidative stress) were significantly enhanced.ConclusionsOur results demonstrate that MBS can play additional roles to prevent heat stress injury. Characterization of the mechanisms underlying mungbean beneficial effects should help in the design of diet therapy strategies to alleviate heat stress, as well as provide reference for searching natural medicines against oxidative stress induced diseases.

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This study was undertaken to determine the effectiveness of apple (Ralls) polyphenol extract (APE) in modulating aluminum chloride (AlCl3) induced hepatotoxicity in rats. The rats were distributed among 4 groups and fed different diets with or without AlCl3 (171.8 mg Al·kg(-1)·day(-1)) and APE (200 mg·kg(-1)·day(-1)) for 10 weeks. The activities of superoxide dismutase and catalase as well as the levels of glutathione and ATP synthesis were decreased by comparison with the control, while the activities of transaminases in serum, the levels of Al, and ATP hydrolysis were increased significantly in the liver of the Al-treated group. Furthermore, abnormal changes in the histological structure of the liver were observed in the Al-treated group. However, these toxic effects of Al were significantly reduced when the rats were fed diets supplemented with APE. This suggests that APE plays a role in the reduction of the toxic effects from Al in rats.