4.6 Article

Lycium Barbarum Polysaccharides and Wolfberry Juice Prevent DEHP-Induced Hepatotoxicity via PXR-Regulated Detoxification Pathway

期刊

MOLECULES
卷 26, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/molecules26040859

关键词

Lycium barbarum polysaccharides; wolfberry juice; di(2-Ethylhexyl) phthalate; pregnane X receptor; intervention

资金

  1. National Key Research and Development Program of Thirteenth Five-Year Plan [2017YFC1601702]
  2. Generic Technique Innovation Team Construction of Modern Agriculture of Guangdong Province [2017LM2152]

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This study demonstrated that Lycium barbarum polysaccharides and wolfberry juice have significant detoxification effects against DEHP-induced hepatotoxicity by activating key detoxifying enzymes. Moreover, the intervention effect of wolfberry juice was more pronounced compared to Lycium barbarum polysaccharides.
Environmental di(2-Ethylhexyl) phthalate (DEHP) is widely used in various industries as a plasticizer, and has been reported to induce reproductive and developmental toxicities in organisms. The purpose of this study was to evaluate the detoxification capacity of Lycium barbarum polysaccharides (LBP) and wolfberry juice (WJ) against DEHP-induced hepatotoxicity. Two groups of rats were purchased to study two different intervention method experiments: LBP (50, 100, 200 mg/kg center dot bw) intervention before DEHP (2000 mg/kg center dot bw) exposure, and LBP (200 mg/kg center dot bw) or WJ (8 mL/kg center dot bw) intervention after DEHP (3000 mg/kg center dot bw) exposure. The rats were exposed to DEHP once, while the intervention lasted for seven days. At the end of the intervention, enzyme-linked immunosorbent assay (ELISA) was used to measure the related index. The LBP intervention before DEHP exposure experiment (the first experimental method) found that LBP group rats showed a strong capacity toward DEHP detoxification, evidenced by the significant upregulation of activities and concentrations of the partner retinoid, X receptor alpha (RXR alpha), and downstream regulators Cytochrome P4502E1 (CYP2E1), Cytochrome P4503A1 (CYP3A1), Glutathione S-Transferase Pi (GSTpi), and UDP-glucuronosyltransferase 1 (UGT1) in a dose-dependent manner. The LBP and WJ intervention after DEHP exposure experiment (the second intervention experiment) found that WJ could downregulate pregnane X receptor (PXR), and upregulate downstream regulators, CYP2E1, CYP3A1, and Glutathione S-Transferase (GST) with the extension of intervention time, to alleviate the toxicity of DEHP. However, the intervention effect of WJ was more obvious than that of LBP. These results suggested that LBP and WJ might be effective detoxification agents against DEHP-induced toxic effects, by activating PXR and PXR-related detoxifying enzymes.

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