ZHAO Danyu, YI Huilan. Mitigative Effect of Grape Skin Extract on Arsenic-induced Small Intestinal Toxicity in a Mouse Model[J]. Science and Technology of Food Industry, 2024, 45(4): 305−312. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023040011.
Citation: ZHAO Danyu, YI Huilan. Mitigative Effect of Grape Skin Extract on Arsenic-induced Small Intestinal Toxicity in a Mouse Model[J]. Science and Technology of Food Industry, 2024, 45(4): 305−312. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023040011.

Mitigative Effect of Grape Skin Extract on Arsenic-induced Small Intestinal Toxicity in a Mouse Model

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  • Received Date: April 02, 2023
  • Available Online: December 18, 2023
  • Objective: To investigate the arsenic-induced small intestinal toxicity and the protective effect of grape skin extract (GSE) against arsenic toxicity. Methods: The small intestinal toxicity was induced by 10 mg/L arsenic via drinking water for 56 days, and was intervened with GSE (150 mg/kg bw and 300 mg/kg bw) by gavage every other day in mice. Small intestine tissue samples of mice were collected and observed by microscope. Glutathione (GSH), malondialdehyde (MDA) and H2O2 contents, as well as total superoxide dismutase (T-SOD) were determined by using commercial kits. qRT-PCR was used to detect expression levels of the tight junction genes and the inflammatory pathway IL-6/JAK2/STAT-3 genes. Results: The results showed that 56 days exposure to 10 mg/L arsenic via drinking water resulted in shortened and disordered intestinal villi, with large numbers of inflammatory cells infiltrating the mucosa propria and submucosa. GSH content and T-SOD activity decreased by 17.1% and 25.2%, while MDA and H2O2 contents increased by 68.8% and 54.3%, respectively (P<0.05) in the small intestinal tissue of arsenic-treated mice. The mRNA levels of IL-6, JAK2 and STAT-3 were upregulated in the small intestinal tissue of mice exposed to arsenic (P<0.05). Meanwhilethe mRNA levels of the ZO-1, ZO-2, occludin, claudin1 and claudin7 genes, which encode the key components of tight junction (TJ) complexes, were downregulated (P<0.05). However, the application of GSE (300 mg/kg bw) significantly alleviated the damage and inflammatory infiltration in small intestine. Compare to the As group, GSH content and T-SOD activity increased by 17.9% and 14.3%. MDA and H2O2 contents decreased by 33.8% and 25.4% (P<0.05). Arsenic-mediated gene expression in the IL-6/JAK2/STAT3 pathway was down-regulated (P<0.05). Moreover, the arsenic-induced down-regulation of TJ genes were markedly relieved in the As+GSE (300 mg/kg bw) group (P<0.05). The As+GSE (150 mg/kg bw) group had a certain alleviating effect on arsenic toxicity, but the difference had no statistical significance (P>0.05). Conclusion: The application of GSE provides significant protection against arsenic-induced small intestinal toxicity by attenuating the oxidative stress and inflammatory responses, and inhibiting the down-regulation of some functional genes.
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