Establishment of a quantitative in vivo method for estimating adipose tissue volumes and the effects of dietary soy sauce oil on adipogenesis in medaka, Oryzias latipes

PLoS One. 2018 Oct 18;13(10):e0205888. doi: 10.1371/journal.pone.0205888. eCollection 2018.

Abstract

Adipose tissue, which is conserved in higher eukaryotes, plays central roles in controlling the body's energy balance, including excess energy storage and energy expenditure during starvation. In adipogenesis, intranuclear receptor, peroxisome proliferator-activated receptor gamma (PPARγ) is a key molecule, and PPARγ agonists can promote adipogenesis. Many studies on the in vitro screening of PPARγ agonists with compounds derived from various materials have been reported; however, in vivo assays for quick examination of these feeding effects have not been established. In this study, we developed a technique using a lipophilic fluorescent reagent, Nile red to quantitatively estimate the adipose tissue volumes by using Japanese rice fish, medaka (Oryzias latipes) and studied effects of dietary soy sauce oil (SSO), which is a discarded by-product from Japanese traditional food and is known to have PPARγ-agonistic activity, on adipogenesis. We found that SSO feeding increased the adipose tissue volumes, and the expression levels of adipogenesis-related genes increased in these medaka larvae. These results suggest that SSO feeding increases the adipose tissue volumes through adipogenesis promotion by PPARγ-agonistic activity in medaka, and medaka is a powerful model for studying adipogenesis. Furthermore, our study also demonstrates the availability of SSO as a dietary additive for farmed fish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activin Receptors, Type I / genetics
  • Activin Receptors, Type I / metabolism
  • Adipogenesis / drug effects*
  • Adipogenesis / genetics
  • Adiponectin / genetics
  • Adiponectin / metabolism
  • Adipose Tissue / drug effects*
  • Adipose Tissue / metabolism
  • Animal Feed / analysis*
  • Animals
  • Animals, Genetically Modified
  • Aquaculture
  • Diet / methods
  • Dietary Fats, Unsaturated / administration & dosage*
  • Energy Metabolism / drug effects
  • Energy Metabolism / genetics
  • Fatty Acid-Binding Proteins / genetics
  • Fatty Acid-Binding Proteins / metabolism
  • Fish Proteins / genetics
  • Fish Proteins / metabolism
  • Fluorescent Dyes / administration & dosage
  • Fluorescent Dyes / chemistry
  • Gene Expression Regulation
  • Genes, Reporter
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Larva / drug effects*
  • Larva / genetics
  • Larva / growth & development
  • Larva / metabolism
  • Lipid Metabolism / drug effects
  • Lipid Metabolism / genetics
  • Oryzias / genetics*
  • Oryzias / growth & development
  • Oryzias / metabolism
  • Oxazines / administration & dosage
  • Oxazines / chemistry
  • PPAR gamma / agonists
  • PPAR gamma / genetics*
  • PPAR gamma / metabolism
  • Soy Foods / analysis

Substances

  • Adiponectin
  • Dietary Fats, Unsaturated
  • Fatty Acid-Binding Proteins
  • Fish Proteins
  • Fluorescent Dyes
  • Oxazines
  • PPAR gamma
  • Green Fluorescent Proteins
  • Activin Receptors, Type I
  • nile red

Grants and funding

The authors would like to thank the local government of Nagahama-city, Shiga, Japan, for funding. Additionally, this work was also supported by JSPS KAKENHI Grant Number 26860197. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.