Prenatal caffeine ingestion induces long-term alterations in scavenger receptor class B type I expression and glucocorticoid synthesis in adult male offspring rat adrenals

Food Chem Toxicol. 2018 Oct:120:24-31. doi: 10.1016/j.fct.2018.06.056. Epub 2018 Jun 26.

Abstract

Caffeine is contained within many drinks and food that are consumed daily. Prenatal caffeine ingestion (PCI) is a risk factor for intrauterine growth retardation (IUGR). We previously observed that PCI inhibits scavenger receptor class B type I (SR-BI)-mediated cholesterol uptake in fetal adrenals, subsequently decreasing glucocorticoid synthesis and inducing IUGR. In the present study, we aimed to investigate the long-term effects of PCI on adrenal glucocorticoid synthesis in adult male offspring rats. After establishing the PCI-induced IUGR, adult male offspring was injected intraperitoneally with 5 mg/kg·d lipopolysaccharide (LPS) for 2 days to induce acute stress. We observed persistent inhibition of SR-BI expression in PCI adrenals before and after stress. Compared with the controls, the PCI offspring had higher corticosterone concentrations after stress. The serum cholesterol concentration was stable without intergroup differences before and after stress. The cholesterol concentration in PCI adrenals showed a higher decrease rate than that of the control after stress. In summary, PCI induced long-term alterations in SR-BI expression and glucocorticoid synthesis in adult male offspring rat adrenals. Cholesterol has to be over-consumed in PCI adrenals against acute stress. This study provides an experimental basis to explain the susceptibility of IUGR offspring to metabolic diseases in adults.

Keywords: Adrenal; Cholesterol supply; Glucocorticoids; Intrauterine growth retardation (IUGR); Prenatal caffeine ingestion (PCI); Scavenger receptor class B type I (SR-BI).

MeSH terms

  • Adrenal Glands / anatomy & histology
  • Adrenal Glands / drug effects*
  • Adrenal Glands / enzymology
  • Adrenal Glands / metabolism
  • Adrenocorticotropic Hormone / blood
  • Animals
  • Caffeine / pharmacology*
  • Cholesterol / blood
  • Cholesterol / metabolism
  • Corticosterone / blood
  • Female
  • Fetal Growth Retardation
  • Glucocorticoids / biosynthesis*
  • Growth / drug effects
  • Hydroxymethylglutaryl CoA Reductases / metabolism
  • Lipopolysaccharides / toxicity
  • Male
  • Pregnancy
  • Prenatal Exposure Delayed Effects*
  • Rats
  • Rats, Wistar
  • Scavenger Receptors, Class B / metabolism*

Substances

  • Glucocorticoids
  • Lipopolysaccharides
  • Scarb1 protein, rat
  • Scavenger Receptors, Class B
  • Caffeine
  • Adrenocorticotropic Hormone
  • Cholesterol
  • Hydroxymethylglutaryl CoA Reductases
  • Corticosterone