Maternal High-Fat Diet Affects the Contents of Eggs and Causes Abnormal Development in the Medaka Fish

Author:

Inoue Yusuke1ORCID,Fukushima Manatsu1,Hirasawa Go12,Furukawa Fumiya3,Takeda Hiroyuki14ORCID,Umatani Chie15ORCID

Affiliation:

1. Department of Biological Sciences, Graduate School of Science, University of Tokyo , Tokyo 113-0033 , Japan

2. Department of Agricultural and Environmental Biology, Graduate School of Agricultural and Life Sciences, University of Tokyo , Tokyo 113-8657 , Japan

3. School of Marine Biosciences, Kitasato University , Kanagawa 252-0373 , Japan

4. Faculty of Life Sciences, Kyoto Sangyo University , Kyoto 603-8555 , Japan

5. Division of Applied Biological Chemistry, Graduate School of Agriculture, Tokyo University of Agriculture and Technology , Tokyo 183-8509 , Japan

Abstract

Abstract Maternal nutritional status can affect development and metabolic phenotypes of progeny in animals. The effects of maternal diet are thought to be mediated mainly by changes inside oocytes such as organelles, maternal RNAs, and metabolites. However, to what extent each factor contributes to offspring phenotypes remains uncertain, especially in viviparous mammalian systems, where factors other than oocytes, such as placenta and milk, need to be considered. Here, using the medaka fish as an oviparous vertebrate model, we examined whether maternal high-fat diet (mHFD) feeding affects offspring development and what kind of changes occur in the contents of mature eggs. We found that mHFD caused the high frequency of embryonic deformities of offspring, accompanied by downregulation of transcription- and translation-related genes and zygotic transcripts at the blastula stage. Transcriptomic and metabolomic analyses of mature eggs suggested decreased catabolism of amino acids and glycogen, moderate upregulation of endoplasmic reticulum stress-related genes, and elevated lipid levels in mHFD eggs. Furthermore, high-fat diet females showed a higher incidence of oocyte atresia and downregulation of egg protein genes in the liver. These data suggest that attenuated amino acid catabolism triggered by decreased yolk protein load/processing, as well as elevated lipid levels inside eggs, are the prime candidates that account for the higher incidence of embryonic deformities in mHFD offspring. Our study presents a comprehensive data on the changes inside eggs in a mHFD model of nonmammalian vertebrates and provides insights into the mechanisms of parental nutritional effects on offspring.

Funder

AMED CREST

JST

JSPS KAKENHI

Lotte Research Promotion Grant

Publisher

The Endocrine Society

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