Maternal separation alters nerve growth factor and corticosterone levels but not the DNA methylation status of the exon 17 glucocorticoid receptor promoter region
Date
2009
Authors
Daniels W.M.U.
Fairbairn L.R.
Van Tilburg G.
McEvoy C.R.E.
Zigmond M.J.
Russell V.A.
Stein D.J.
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Abstract
Separating rat pups from their mothers during the early stages of life is an animal model commonly used to study the development of psychiatric disorders such as anxiety and depression. The present study investigated how soon after the termination of the maternal separation period behavioural and neuroendocrine abnormalities relevant to above-mentioned illnesses would manifest. Sprague Dawley rat pups were subjected to maternal separation (3 h per day from postnatal day 2 through 14) and their behaviour and HPA axis activity determined 7 d later. We also measured nerve growth factor levels in their hippocampi and assessed the DNA methylation status of the promoter region of exon 17 of the glucocorticoid receptor in this brain region. As early as 7 d after the termination of the adverse event, a change in behaviour was observed that was associated with increased plasma corticosterone release and elevated nerve growth factor levels in the hippocampus. No alteration in the methylation status of the exon 17 glucocorticoid receptor promoter region was observed. Our data indicate that early life adversity may lead to the rapid development of abnormal behaviours and HPA axis dysregulation though no epigenetic changes to the exon 17 glucocorticoid receptor promoter region occurred. We further propose that the observed increased neurotrophin levels reflect compensatory mechanisms that attempt to combat the long-term deleterious effects of maternal separation. © 2009 Springer Science+Business Media, LLC.
Description
Keywords
corticosterone, DNA, glucocorticoid receptor, nerve growth factor, neurotrophin, animal behavior, animal experiment, animal tissue, anxiety disorder, article, controlled study, corticosterone release, depression, DNA methylation, enzyme linked immunosorbent assay, exon, hippocampus, hypothalamus hypophysis adrenal system, life stress, locomotion, maternal deprivation, neuroendocrine system, newborn, nonhuman, open field behavior, polymerase chain reaction, promoter region, rat, Animals, Base Sequence, Behavior, Animal, Corticosterone, Disease Models, Animal, DNA Methylation, Epigenesis, Genetic, Exons, Female, Hippocampus, Hypothalamo-Hypophyseal System, Male, Maternal Deprivation, Molecular Sequence Data, Mood Disorders, Nerve Growth Factor, Neurosecretory Systems, Promoter Regions, Genetic, Rats, Rats, Sprague-Dawley, Receptors, Glucocorticoid, Stress, Psychological, Animalia, Rattus
Citation
Metabolic Brain Disease
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