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
Main Authors: Kolber, Benedict J, Boyle, Maureen P, Wieczorek, Lindsay, Kelley, Crystal L, Onwuzurike, Chiamaka C, Nettles, Sabin A, Vogt, Sherri K, Muglia, Louis J
Format: Journal Article
Language:English
Published: United States Soc Neuroscience 17-02-2010
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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.
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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  fullname: Vogt, Sherri K
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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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pubmed
highwire
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StartPage 2571
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
URI http://www.jneurosci.org/cgi/content/abstract/30/7/2571
https://www.ncbi.nlm.nih.gov/pubmed/20164342
https://pubmed.ncbi.nlm.nih.gov/PMC2969849
Volume 30
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