4.6 Article

DHA Suppresses Hepatic Lipid Accumulation via Cyclin D1 in Zebrafish

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FRONTIERS IN NUTRITION
卷 8, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnut.2021.797510

关键词

high-fat diet; DHA; lipid accumulation; Cyclin D1; gut microbiota

资金

  1. National Natural Science Foundation of China [NSFC 31925038, 32061133004]
  2. National Key R&D Program of China [2018YFD0900400]

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This study investigated the effects of docosahexaenoic acid (DHA) on fatty liver in zebrafish. The results showed that supplementation of DHA reduced hepatic lipid synthesis and promoted lipid beta-oxidation through Cyclin D1 inhibition. Furthermore, DHA facilitated lipid beta-oxidation through gut microbiota. These findings reveal the lipid-lowering effects of DHA and emphasize the importance of fatty acid composition in formulating high-fat diets for fish.
With the widespread use of high-fat diets (HFDs) in aquaculture, fatty livers are frequently observed in many fish species. The aim of this study was to investigate if docosahexaenoic acid (DHA) could be used to reduce the fatty liver in zebrafish generated by a 16% soybean oil-HFD over 2 weeks of feeding. The DHA was added to iso-lipidic HFD at 0.5, 1.0, and 2.0% of diet. Supplementation of DHA reduced growth and feed efficiency in a dose dependent manner being lowest in the HFDHA2.0 group. Hepatic triglyceride (TG) in zebrafish fed 0.5% DHA-supplemented HFD (HFDHA0.5) was significantly lower than in the HFD control. Transcriptional analyses of hepatic genes showed that lipid synthesis was reduced, while fatty acid beta-oxidation was increased in the HFDHA0.5 group. Furthermore, the expression of Cyclin D1 in liver of zebrafish fed HFDHA0.5 was significantly reduced compared to that in fish fed HFD. In zebrafish liver cells, Cyclin D1 knockdown and blocking of Cyclin D1-CDK4 signal led to inhibited lipid biosynthesis and elevated lipid beta-oxidation. Besides, DHA-supplemented diet resulted in a rich of Proteobacteria and Actinobacteriota in gut microbiota, which promoted lipid beta-oxidation but did not alter the expression of Cyclin D1 in germ-free zebrafish model. In conclusion, DHA not only inhibits hepatic lipid synthesis and promotes lipid beta-oxidation via Cyclin D1 inhibition, but also facilitates lipid beta-oxidation via gut microbiota. This study reveals the lipid-lowering effects of DHA and highlights the importance of fatty acid composition when formulating fish HFD.

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