Author:
Jacombs Anita,Pollard Irina,Ryan John,Loupis Anne
Abstract
Models for studying prenatal drug-induced
intrauterine growth retardation (IUGR) have, without exception, measured
growth-related factors in the postimplantation embryo, fetus or neonate.
Therefore, it is not known whether effects of drug exposure on growth and
metabolism begin early in the preimplantation embryo, or whether IUGR is
exclusively a postimplantation phenomenon. The present study investigates
whether caffeine, a drug known to induce a dose-dependent fetal IUGR, affects
embryo development before and/or after implantation or is exclusively a
fetal phenomenon. Preimplantation embryo assessment (with treatment from Days
2 to 4 of pregnancy) included glucose utilization, cell number evaluation and
stage of development (morula to hatched blastocyst); whereas, postimplantation
embryo assessment (treatment from Days 2 to 10, 10.5 or 11 of pregnancy)
included somite number evaluation and extent of neural tube closure, as seen
using scanning electron microscopy. Comparing control preimplantation embryos
with those exposed to 30 and 60 mg kg –1 caffeine did not reveal any
effects of caffeine exposure, as assessed on Day 5 of gestation. However,
postimplantation embryo development assessed on Day 12 of gestation revealed
that caffeine exposure of 15 and 30 mg kg –1 significantly reduced, at
both dosage levels, somite number and the extent of neural tube closure. In
addition, comparisons of control and experimental groups revealed that in the
high-dose caffeine group the forebrain cavity was significantly enlarged and
bounded by a reduced, irregularly aligned neuroepithelium. The findings
suggest that IUGR is a phenomenon first identifiable during late
postimplantation embryogenesis and continues in fetal life.
Subject
Developmental Biology,Endocrinology,Genetics,Molecular Biology,Animal Science and Zoology,Reproductive Medicine,Biotechnology
Cited by
10 articles.
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