Dietary administration of black raspberries modulates arsenic biotransformation and reduces urinary 8-oxo-2′-deoxyguanosine in mice

Arsenic in drinking water is a worldwide public health problem due to its pathogenic induction of oxidative stress in various organ systems. Phytochemicals present in polyphenolic-rich fruits such as black raspberries (BRBs) have diverse health benefits, including antioxidation and modulation of enz...

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Veröffentlicht in:Toxicology and applied pharmacology 2019-08, Vol.377, p.114633, Article 114633
Hauptverfasser: Tu, Pengcheng, Xue, Jingchuan, Bian, Xiaoming, Chi, Liang, Gao, Bei, Leng, Jiapeng, Ru, Hongyu, Knobloch, Thomas J., Weghorst, Christopher M., Lu, Kun
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Sprache:eng
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Zusammenfassung:Arsenic in drinking water is a worldwide public health problem due to its pathogenic induction of oxidative stress in various organ systems. Phytochemicals present in polyphenolic-rich fruits such as black raspberries (BRBs) have diverse health benefits, including antioxidation and modulation of enzymes in xenobiotic metabolism. We used a mouse model combined with a standardized BRB-rich diet to investigate the impact of BRB consumption on arsenic biotransformation. We observed a significant reduction of urinary 8-oxo-2′-deoxyguanosine (8-oxodG) together with elevated levels of methylation and urinary excretion of arsenic in mice concurrently fed BRBs upon arsenic exposure. Moreover, enzyme expression and liver metabolites involved in arsenic metabolism were found to be different between mice on BRB and control diets with arsenic exposure. These data indicate that BRB consumption affected arsenic biotransformation in vivo likely via alterations in related metabolic enzymes and cofactors, providing evidence on reduction of arsenic toxicity by consumption of BRBs. •Dietary black raspberries alleviated arsenic-induced oxidative stress in mice.•Methylation and urinary excretion of arsenic were significantly increased.•Alterations in levels of enzymes and cofactors in arsenic metabolism were observed.
ISSN:0041-008X
1096-0333
DOI:10.1016/j.taap.2019.114633