Resveratrol ameliorates diet-induced dysregulation of lipid metabolism in zebrafish (Danio rerio)

PLoS One. 2017 Jul 7;12(7):e0180865. doi: 10.1371/journal.pone.0180865. eCollection 2017.

Abstract

Defective lipid metabolism is associated with increased risk of various chronic diseases, such as obesity, cardiovascular diseases, and diabetes. Resveratrol (RSV), a natural polyphenol, has been shown the potential of ameliorating disregulations of lipid metabolism. The objective of this study was to investigate the effects of feed intake and RSV on lipid metabolism in zebrafish (Danio rerio). The adult males were randomly allocated to 6 groups: control (Con, 8 mg cysts/fish/day), control with 20 μmol/L RSV (Con+RSV), calorie restriction (CR, 5 mg cysts/fish/day), calorie restriction with RSV (CR+RSV), overfeed (OF, 60 mg cysts/fish/day), and overfeed with RSV (OF+RSV) groups. The treatment period was 8 weeks. Results showed that CR reduced body length, body weight, and condition factor of zebrafish. CR reduced levels of plasma triglyceride (TG) and induced protein expression of phosphorylated AMP-activated protein kinase-α (pAMPKα), silent information regulator 2 homolog 1 (Sirt1), and peroxisome proliferator activated receptor gamma coactivator-1α (PGC1α). RSV attenuated CR-induced pAMPKα/AMPKαincreases. RSV increased levels of Sirt1 protein in the OF zebrafish, and decreased OF-induced increase in peroxisome proliferator-activated receptor-γ (PPARγ) protein level. Additionally, RSV down-regulated caveolin-1 and up-regulated microtubule-associated protein 1 light chain 3 -II (LC3-II) protein levels in OF zebrafish. In conclusion, these results suggest that 1) CR reduces plasma TG level through activation of the AMPKα-Sirt1- PGC1α pathway; 2) under different dietary stress conditions RSV might regulate AMPK phosphorylation bi-directionally; 3) RSV might regulate lipid metabolism through the AMPKα-Sirt1-PPARγ pathway in OF zebrafish.

MeSH terms

  • AMP-Activated Protein Kinase Kinases
  • Animals
  • Antioxidants / pharmacology*
  • Caloric Restriction / adverse effects
  • Caveolin 1 / genetics
  • Caveolin 1 / metabolism
  • Diet / methods*
  • Eating / physiology
  • Female
  • Gene Expression Regulation / drug effects*
  • Lipid Metabolism / drug effects*
  • Lipid Metabolism / genetics
  • Male
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Phosphorylation
  • Protein Kinases / genetics
  • Protein Kinases / metabolism
  • Resveratrol
  • Signal Transduction
  • Sirtuin 1 / genetics
  • Sirtuin 1 / metabolism
  • Stilbenes / pharmacology*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Triglycerides / metabolism
  • Zebrafish
  • Zebrafish Proteins / genetics
  • Zebrafish Proteins / metabolism

Substances

  • Antioxidants
  • Caveolin 1
  • Microtubule-Associated Proteins
  • PPAR gamma
  • Stilbenes
  • Transcription Factors
  • Triglycerides
  • Zebrafish Proteins
  • map1lc3b protein, zebrafish
  • peroxisome proliferator activated receptor gamma coactivator-1alpha, zebrafish
  • Protein Kinases
  • AMP-Activated Protein Kinase Kinases
  • Sirtuin 1
  • Resveratrol

Grants and funding

This work was supported by National Natural Science Foundation of China: Grant No.81273060; No.81373007; No.81302423, https://isisn.nsfc.gov.cn/egrantindex/funcindex/prjsearch-list; National Training Programs of Innovation and Entrepreneurship for Undergraduates: Grant No. 201310343013.