Maternal glucocorticoid elevation and associated blood metabonome changes might be involved in metabolic programming of intrauterine growth retardation in rats exposed to caffeine prenatally
Creators
- 1. Department of Pharmacology, Basic Medical School of Wuhan University, Wuhan 430071 (China)
- 2. Hubei Provincial Key Laboratory of Developmentally Originated Diseases, Wuhan 430071 (China)
- 3. Center for Reproductive Medicine, Zhongnan Hospital of Wuhan University, Wuhan 430071 (China)
- 4. Department of Electronic Science, Fujian Provincial Key Laboratory of Plasma and Magnetic Resonance, Xiamen University, Xiamen 361005 (China)
Description
Our previous studies demonstrated that prenatal caffeine exposure causes intrauterine growth retardation (IUGR), fetuses are over-exposed to high levels of maternal glucocorticoids (GC), and intrauterine metabolic programming and associated metabonome alteration that may be GC-mediated. However, whether maternal metabonomes would be altered and relevant metabolite variations might mediate the development of IUGR remained unknown. In the present studies, we examined the dose- and time-effects of caffeine on maternal metabonome, and tried to clarify the potential roles of maternal GCs and metabonome changes in the metabolic programming of caffeine-induced IUGR. Pregnant rats were treated with caffeine (0, 20, 60 or 180 mg/kg · d) from gestational days (GD) 11 to 20, or 180 mg/kg · d caffeine from GD9. Metabonomes of maternal plasma on GD20 in the dose–effect study and on GD11, 14 and 17 in the time–course study were analyzed by 1H nuclear magnetic resonance spectroscopy, respectively. Caffeine administration reduced maternal weight gains and elevated both maternal and fetal corticosterone (CORT) levels. A negative correlation between maternal/fetal CORT levels and fetal bodyweight was observed. The maternal metabonome alterations included attenuated metabolism of carbohydrates, enhanced lipolysis and protein breakdown, and amino acid accumulation, suggesting GC-associated metabolic effects. GC-associated metabolite variations (α/β-glucoses, high density lipoprotein-cholesterol, β-hydroxybutyrate) were observed early following caffeine administration. In conclusion, prenatal caffeine exposure induced maternal GC elevation and metabonome alteration, and maternal GC and relevant discriminatory metabolites might be involved in the metabolic programming of caffeine-induced IUGR. - Highlights: • Prenatal caffeine exposure elevated maternal blood glucocorticoid levels. • Prenatal caffeine exposure altered maternal blood metabonomes. • Maternal metabonome alterations were associated with glucocorticoid elevation. • Maternal metabonomes were altered at early stage after caffeine exposure. • Maternal glucocorticoid and associated metabolites may be involved in fetal programming
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2014.01.007Additional details
Identifiers
- DOI
- 10.1016/j.taap.2014.01.007;
- PII
- S0041-008X(14)00015-5;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 275
- Journal Issue
- 2
- Journal Page Range
- p. 79-87
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46129717
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- AMINO ACIDS; BLOOD; CAFFEINE; CHOLESTEROL; CORTICOSTERONE; FETUSES; GLUCOSE; HYDROGEN 1; HYPOTHALAMUS; LIPOPROTEINS; METABOLISM; METABOLITES; NUCLEAR MAGNETIC RESONANCE; RATS
- Descriptors DEC
- ADRENAL HORMONES; ALDEHYDES; ANALEPTICS; ANIMALS; AROMATICS; AZAARENES; BIOLOGICAL MATERIALS; BODY; BODY FLUIDS; BRAIN; CARBOHYDRATES; CARBOXYLIC ACIDS; CENTRAL NERVOUS SYSTEM; CENTRAL NERVOUS SYSTEM AGENTS; CORTICOSTEROIDS; DRUGS; GLUCOCORTICOIDS; HETEROCYCLIC COMPOUNDS; HEXOSES; HORMONES; HYDROGEN ISOTOPES; HYDROXY COMPOUNDS; ISOTOPES; KETONES; LIGHT NUCLEI; LIPIDS; MAGNETIC RESONANCE; MAMMALS; MATERIALS; MONOSACCHARIDES; NERVOUS SYSTEM; NUCLEI; ODD-EVEN NUCLEI; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; ORGANS; PREGNANES; PROTEINS; PURINES; RESONANCE; RODENTS; SACCHARIDES; STABLE ISOTOPES; STEROID HORMONES; STEROIDS; STEROLS; VERTEBRATES; XANTHINES
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.