Transient Early-Life Forebrain Corticotropin-Releasing Hormone Elevation Causes Long-Lasting Anxiogenic and Despair-Like Changes in Mice
During development, early-life stress, such as abuse or trauma, induces long-lasting changes that are linked to adult anxiety and depressive behavior. It has been postulated that altered expression of corticotropin-releasing hormone (CRH) can at least partially account for the various effects of str...
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Published in: | The Journal of neuroscience Vol. 30; no. 7; pp. 2571 - 2581 |
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Abstract | During development, early-life stress, such as abuse or trauma, induces long-lasting changes that are linked to adult anxiety and depressive behavior. It has been postulated that altered expression of corticotropin-releasing hormone (CRH) can at least partially account for the various effects of stress on behavior. In accord with this hypothesis, evidence from pharmacological and genetic studies has indicated the capacity of differing levels of CRH activity in different brain areas to produce behavioral changes. Furthermore, stress during early life or adulthood causes an increase in CRH release in a variety of neural sites. To evaluate the temporal and spatial specificity of the effect of early-life CRH exposure on adult behavior, the tetracycline-off system was used to produce mice with forebrain-restricted inducible expression of CRH. After transient elevation of CRH during development only, behavioral testing in adult mice revealed a persistent anxiogenic and despair-like phenotype. These behavioral changes were not associated with alterations in adult circadian or stress-induced corticosterone release but were associated with changes in CRH receptor type 1 expression. Furthermore, the despair-like changes were normalized with antidepressant treatment. Overall, these studies suggest that forebrain-restricted CRH signaling during development can permanently alter stress adaptation leading to increases in maladaptive behavior in adulthood. |
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AbstractList | During development, early-life stress, such as abuse or trauma, induces long-lasting changes that are linked to adult anxiety and depressive behavior. It has been postulated that altered expression of corticotropin-releasing hormone (CRH) can at least partially account for the various effects of stress on behavior. In accord with this hypothesis, evidence from pharmacological and genetic studies has indicated the capacity of differing levels of CRH activity in different brain areas to produce behavioral changes. Furthermore, stress during early life or adulthood causes an increase in CRH release in a variety of neural sites. To evaluate the temporal and spatial specificity of the effect of early-life CRH exposure on adult behavior, the tetracycline-off system was used to produce mice with forebrain-restricted inducible expression of CRH. After transient elevation of CRH during development only, behavioral testing in adult mice revealed a persistent anxiogenic and despair-like phenotype. These behavioral changes were not associated with alterations in adult circadian or stress-induced corticosterone release but were associated with changes in CRH receptor type 1 expression. Furthermore, the despair-like changes were normalized with antidepressant treatment. Overall, these studies suggest that forebrain-restricted CRH signaling during development can permanently alter stress adaptation leading to increases in maladaptive behavior in adulthood. |
Author | Kolber, Benedict J Boyle, Maureen P Kelley, Crystal L Nettles, Sabin A Vogt, Sherri K Muglia, Louis J Onwuzurike, Chiamaka C Wieczorek, Lindsay |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20164342$$D View this record in MEDLINE/PubMed |
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Notes | M. P. Boyle's present address: Allen Institute for Brain Science, Seattle, WA 02114. C. L. Kelley's present address: University of Kansas, Wichita, KS 66045. |
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Snippet | During development, early-life stress, such as abuse or trauma, induces long-lasting changes that are linked to adult anxiety and depressive behavior. It has... |
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SubjectTerms | Adaptation, Ocular - drug effects Adaptation, Ocular - genetics Age Factors Analysis of Variance Animals Animals, Newborn Antidepressive Agents - pharmacology Antidepressive Agents - therapeutic use Anxiety - drug therapy Anxiety - etiology Anxiety - genetics Behavior, Animal - physiology Calcium-Calmodulin-Dependent Protein Kinase Type 2 - genetics Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism Circadian Rhythm - drug effects Circadian Rhythm - genetics Corticotropin-Releasing Hormone - genetics Corticotropin-Releasing Hormone - metabolism Depression - drug therapy Depression - etiology Depression - genetics Disease Models, Animal Doxycycline - administration & dosage Embryo, Mammalian Exploratory Behavior - drug effects Exploratory Behavior - physiology Gene Expression Regulation, Developmental - drug effects Gene Expression Regulation, Developmental - genetics Gene Expression Regulation, Developmental - physiology Growth Hormone - metabolism Hindlimb Suspension - methods Hypothalamo-Hypophyseal System - growth & development Hypothalamo-Hypophyseal System - metabolism Imipramine - pharmacology Imipramine - therapeutic use Mice Mice, Inbred C57BL Mice, Transgenic Mutation - genetics Pituitary-Adrenal System - growth & development Pituitary-Adrenal System - metabolism Prosencephalon - embryology Prosencephalon - growth & development Prosencephalon - metabolism Radioimmunoassay - methods Reaction Time - genetics Receptors, Corticotropin-Releasing Hormone - genetics Receptors, Corticotropin-Releasing Hormone - metabolism |
Title | Transient Early-Life Forebrain Corticotropin-Releasing Hormone Elevation Causes Long-Lasting Anxiogenic and Despair-Like Changes in Mice |
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