4.7 Article

Effects on the liver lipidome of rat offspring prenatally exposed to bisphenol A

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SCIENCE OF THE TOTAL ENVIRONMENT
卷 759, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.scitotenv.2020.143466

关键词

Developmental exposure; Mass spectrometry-based lipidomics; Multi-omics integration; Sex-dependent effects; Age-dependent effects; Bisphenol A

资金

  1. Japan Society for the Promotion of Science (JSPS) [26220103, 19H01150, 18K18199]
  2. Ministry of Education, Culture, Sports, Science and Technology, Japan (MEXT)
  3. National Research Foundation of Korea (NRF) from Ministry of Education, Science and Technology, Korea [2016R1A2B4007714, 2019R1A2C1084556]
  4. Ministry of Environment, Korea [H117-00137-0702]
  5. Grants-in-Aid for Scientific Research [19H01150, 18K18199] Funding Source: KAKEN
  6. National Research Foundation of Korea [2019R1A2C1084556, 2016R1A2B4007714] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The study found that prenatal exposure to BPA led to decreased total lipid content in female offspring, while levels of fatty acids, acylcarnitines, and monoacylglycerols significantly increased. Compared to females exposed to BPA, males showed opposite changes in phospholipids and sphingolipids. Although the alterations in lipid profiles continued until PND60, the effects on body weight and total lipid content were mitigated in the later stage.
Bisphenol A (BPA) is a well-known endocrine disruptor that has obesogenic properties. We have previously reported sex- and age-dependent changes in hepatic transcriptome and proteome of several lipid homeostasis-related genes in rat offspring prenatally exposed to BPA. To further understand the impacts of prenatal BPA exposure, we analyzed lipidomic profiles in the postnatal day (PND) 21 and 60 rats using a high-resolution QTOF mass spectrometer coupled with a HPLC system. We found that the total lipid content was significantly decreased in PND21 females prenatally exposed to 5000 mu g/kg bw/day of BPA. Levels of total fatty acids, acylcarnitines, and monoacylglycerols significantly increased in both female and male BPA-exposed rats at PND21. An elevation in total cholesterol esters and reductions in triacylglycerols and monogalactosyl diacylglycerols were found only in PND21 females prenatally exposed to BPA. Interestingly, opposite responses were observed for phospholipids and sphingolipids between PND21 females and males following BPA exposure. The effects on the body weight and total lipid content were mitigated in the latter stage, although the alterations of lipid profiles continued until PND60. A Data Integration Analysis for Biomarker discovery using Latent cOmponents (DIABLO) revealed a high correlation of the lipidome with our previously published transcriptome data. DIABLO also identified potential biomarkers of prenatal exposure to BPA; glycerol-3-phosphate dehydrogenase 1 (Gpd1) and glyceronephosphate O-acyltransferase (Gnpat), which are involved in the glycerophospholipid metabolism, in females and males, respectively. Collectively, we highlighted the sex- and age-dependent effects of prenatal BPA exposure on hepatic lipid homeostasis in rat offspring. (C) 2020 Elsevier B.V. All rights reserved.

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