4.7 Article

Protective effect of low molecular-weight seleno-aminopolysaccharides against H2O2-induecd oxidative stress in intestinal epithelial cells

期刊

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijbiomac.2018.01.191

关键词

Low molecular-weight seleno-aminopolysaccharide; Antioxidant activity; Keap1/Nrf2 signaling pathway

资金

  1. Zhejiang Provincial Natural Science Foundation of China [LY17C170001, LY18D060002]
  2. National Natural Science Foundation of China [31301982]
  3. International Science & Technology Cooperation Program of China [2015DFA30980]
  4. Scientific and Technological Project of Zhejiang Ocean University [X12M05]
  5. Key Scientific and Technological Project of Zhejiang Ocean University [X12ZD08]

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Organoselemium compounds possess strong antioxidant activity as well as protecting cells from DNA damage, mitochondrial injury, lipid peroxidation, protein denaturation and cell death. Herein, we used an in vitro oxidative model to further investigate the antioxidant effects of a novel organoselemium compound, low molecular weight seleno-aminopolysaccharides (ISA) in intestinal porcine epithelial cells (IPEC-1), and the molecular mechanisms of these effects. Analysis by MTT assay showed that ISA could significantly increase the viability of IPEC-1 cells compared to cells exposed to H2O2. We found that the levels of different antioxidant enzymes could dramatically increase in ISA pretreatment group compared to H2O2 treatment group. Furthermore, ISA significantly increased the gene expression of antioxidant enzymes and phase 2 detoxifying enzymes in IPEC-1 cells, as measured by qRT-PCR. In addition, ISA up-regulated the expression level of intracellular transcription factor NF-E2-related factor 2 (Nrf2) and inhibited the level of kelch-like ECH-assodated protein 1 (Keap1) with western blot analysis. Collectively, the present study suggested that ISA has the protective effect of IPEC-1 cells against H2O2-induecd oxidative stress, and its mechanism may be related to activation of Keap1/Nrf2 signaling pathway in intestinal epithelial cells. (C) 2018 Elsevier B.V. All rights reserved.

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