Transcriptomics and metabonomics analyses of maternal DEHP exposure on male offspring

Environ Sci Pollut Res Int. 2018 Sep;25(26):26322-26329. doi: 10.1007/s11356-018-2596-8. Epub 2018 Jul 6.

Abstract

The objectives of this study were to evaluate the effect of maternal Di-2-ethylhexyl phthalate (DEHP) exposure on male offspring and to explore the mechanism of changes with the metabolic alterations and differential genes. Pregnant female Sprague-Dawley (SD) rats were intragastrically administered with 600 mg/kg body weight of DEHP or corn oil (CON) throughout pregnancy and lactation. The growth of male offspring was investigated until 14 weeks old, the indices of blood were detected, and mechanism was studied using metabonomics and transcriptomics. Compared with the CON group, body weight, body length, food intake, body fat weight, Lee's index, organ coefficient, blood lipids, and oral glucose tolerance test (OGTT) of male offspring were not significantly changed in maternal DEHP group. However, serum biochemical indexes such as alanine transaminase (ALT), total protein (TP), albumin (ALB), blood urea nitrogen (BUN), and creatinine (CREA) were markedly reduced in maternal DEHP group (p < 0.05). In addition, insulin level was elevated and catalase (CAT) level was decreased notably in maternal DEHP group compared with the CON group (p < 0.05). Furthermore, thyroxine (T4) level was lower and thyroid stimulating hormone (TSH) level was higher in maternal DEHP group (p < 0.05). Metabonomics revealed seven principal metabolites were identified, including increased L-allothreonine, creatine, uric acid, retinyl ester, L-palmitoylcarnitine, and decreased glycocholic acid and LysoPC (18:3). Transcriptomics displayed 35 differential genes were involved in the mechanism of maternal DEHP exposure. Therefore, this research confirms the effect of a certain dose of maternal DEHP exposure on male offspring and understands exactly the mechanism of these changes with metabonomics and transcriptomics.

Keywords: DEHP; Insulin; Maternal exposure; Metabonomics; Thyroxine; Transcriptomics.

MeSH terms

  • Adipose Tissue
  • Animals
  • Antioxidants / metabolism
  • Body Weight
  • Diethylhexyl Phthalate / toxicity*
  • Eating
  • Female
  • Insulin Resistance
  • Lactation
  • Lipids / blood
  • Male
  • Maternal Exposure
  • Metabolome*
  • Metabolomics
  • Plasticizers
  • Pregnancy
  • Prenatal Exposure Delayed Effects*
  • Rats
  • Rats, Sprague-Dawley
  • Thyroid Hormones / blood
  • Transcriptome*

Substances

  • Antioxidants
  • Lipids
  • Plasticizers
  • Thyroid Hormones
  • Diethylhexyl Phthalate