4.7 Article

Effects of Dietary Selenium and Oxidized Fish Oils on Intestinal Lipid Metabolism and Antioxidant Responses of Yellow Catfish Pelteobagrus fulvidraco

期刊

ANTIOXIDANTS
卷 11, 期 10, 页码 -

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MDPI
DOI: 10.3390/antiox11101904

关键词

selenium; selenoprotein; oxidized fish oils; oxidative stress; lipid metabolism; vertebrates

资金

  1. National Key R&D Program of China [2018YFD0900400]

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This study investigated the effects of selenium and oxidized fish oil on intestinal lipid metabolism and antioxidant responses in yellow catfish. The results showed that selenium supplementation reduced intestinal tissue damage and lipid accumulation induced by oxidized fish oils. Additionally, selenium alleviated oxidative stress and affected the expression of intestinal selenoproteins. Mechanistically, selenium and oxidized eicosapentaenoic acid influenced glutathione content by affecting the DNA binding ability of activating transcription factor 3 (ATF3) to the slc7a11 promoter.
Currently, the effect of selenium and oxidized fish oil interactions on the intestinal lipid metabolism and antioxidant responses of fish remains unknown. Herein, yellow catfish Pelteobagrus fulvidraco (weight: 3.99 +/- 0.01 g) were used as experimental animals and were fed four diets: an adequate amount of selenium (0.25 mg kg(-1)) with fresh fish oil (A-Se+FFO), an adequate amount of selenium with oxidized fish oil (A-Se+OFO), a high amount of selenium (0.50 mg kg(-1)) with fresh fish oil (H-Se+FFO), and a high amount of selenium with oxidized fish oil (H-Se+OFO). The feeding experiment was conducted for 10 weeks. The results showed that selenium supplementation alleviated the intestinal tissue damage and reduced the lipid accumulation that was induced by oxidized fish oils. Meanwhile, we also found that 0.50 mg kg(-1) selenium reduced the oxidative stress that is caused by oxidized fish oils through increasing the GSH and the activity and mRNA expression of antioxidant enzymes. Dietary selenium and oxidized fish oils also affected the mRNA expression of intestinal selenoproteins including selenow2a, selenop2, and selenot2. Mechanistically, Se and oxidized eicosapentaenoic acid (oxEPA) influenced the GSH content by affecting the DNA binding ability of activating transcription factor (ATF) 3 to the slc7a11 promoter. For the first time, our results suggested that selenium alleviated the oxidized fish oil-induced intestinal lipid deposition and the oxidative stress of the fish. We also elucidated the novel mechanism of selenium increasing the GSH content by affecting the interaction of ATF3 and the slc7a11 promoter.

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