Dietary fenofibrate attenuated high-fat-diet-induced lipid accumulation and inflammation response partly through regulation of pparα and sirt1 in juvenile black seabream (Acanthopagrus schlegelii)

Dev Comp Immunol. 2020 Aug:109:103691. doi: 10.1016/j.dci.2020.103691. Epub 2020 Apr 3.

Abstract

An 8-week feeding trail was conducted in Acanthopagrus schlegelii with an initial body weight of 8.34 ± 0.01g. Three isonitrogenous diets were formulated, (1) Control: medium-fat diet (12%); (2) HFD: high-fat diet (18%); (3) HFD + FF: high-fat diet with fenofibrate (0.15%). Liver histological analysis revealed that, compared to HFD, vacuolar fat drops were smaller and fewer in fish fed fenofibrate. Expression of lipid catabolism regulator peroxisome proliferator-activated receptor alpha (pparα) was up-regulated by fenofibrate compared with HFD. In addition, fenofibrate significantly increased the expression level of silent information regulator 1 (sirt1). Meanwhile, the expression level of anti-inflammatory cytokine interleukin 10 (il-10) in intestine was up-regulated, while pro-inflammatory cytokine interleukin 1β (il-1β) in liver and intestine were down-regulated by dietary fenofibrate supplementation. Overall, the present study indicated that fenofibrate reduced fat deposition and attenuated inflammation response caused by HFD partly through a pathway involving regulation of pparα and sirt1.

Keywords: Fenofibrate; High-fat diet; Inflammation response; pparα; sirt1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytokines / metabolism
  • Diet, High-Fat / adverse effects*
  • Down-Regulation / drug effects
  • Fenofibrate / pharmacology*
  • Inflammation / drug therapy*
  • Inflammation / metabolism
  • Lipid Metabolism / drug effects*
  • Lipids / physiology
  • Liver / drug effects
  • Liver / metabolism
  • PPAR alpha / metabolism*
  • Perciformes / metabolism
  • Sea Bream / metabolism*
  • Signal Transduction / drug effects
  • Sirtuin 1 / metabolism*
  • Up-Regulation / drug effects

Substances

  • Cytokines
  • Lipids
  • PPAR alpha
  • Sirtuin 1
  • Fenofibrate