Amygdaloid pERK1/2 in corticotropin-releasing hormone overexpressing mice under basal and acute stress conditions

Corticotropin-releasing hormone (CRH) coordinates neuroendocrine and behavioral adaptations to stress. Acute CRH administration in vivo activates extracellular signal-regulated kinase 1/2 (ERK1/2) in limbic brain areas, acting through the CRH receptor type 1 (CRH-R1). In the present study, we used C...

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Autores principales: Silberstein, S., Vogl, A.M., Refojo, D., Senin, S.A., Wurst, W., Holsboer, F., Deussing, J.M., Arzt, E.
Formato: JOUR
Materias:
CRF
CRH
ERK
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03064522_v159_n2_p610_Silberstein
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spelling todo:paper_03064522_v159_n2_p610_Silberstein2023-10-03T15:22:23Z Amygdaloid pERK1/2 in corticotropin-releasing hormone overexpressing mice under basal and acute stress conditions Silberstein, S. Vogl, A.M. Refojo, D. Senin, S.A. Wurst, W. Holsboer, F. Deussing, J.M. Arzt, E. CRF CRH CRH receptor ERK HPA axis mitogen activated protein kinase 1 mitogen activated protein kinase 3 acute stress amygdaloid nucleus animal experiment article brain region controlled study immunohistochemistry in situ hybridization mouse nonhuman priority journal protein expression Amphibian Proteins Amygdala Animals Autoradiography Corticosterone Corticotropin-Releasing Hormone Disease Models, Animal Gene Expression Regulation, Enzymologic Iodine Isotopes Male Mice Mice, Transgenic Mitogen-Activated Protein Kinase 3 Peptide Hormones Protein Binding Radioimmunoassay Receptors, Corticotropin-Releasing Hormone Restraint, Physical Stress, Psychological Time Factors Corticotropin-releasing hormone (CRH) coordinates neuroendocrine and behavioral adaptations to stress. Acute CRH administration in vivo activates extracellular signal-regulated kinase 1/2 (ERK1/2) in limbic brain areas, acting through the CRH receptor type 1 (CRH-R1). In the present study, we used CRH-COE-Cam mice that overexpress CRH in limbic-restricted areas, to analyze the effect of chronic CRH overexpression on ERK1/2 activation. By immunohistochemistry and confocal microscopy analysis we found that pERK1/2 levels in the basolateral amygdala (BLA) were similar in control and CRH overexpressing mice under basal conditions. Acute stress caused comparably increased levels of corticosterone in both control (CRH-COEcon-Cam) and CRH overexpressing (CRH-COEhom-Cam) animals. CRH-COEhom-Cam mice after stress showed reduced pERK1/2 immunoreactivity in the BLA compared to CRH-COEhom-Cam animals under basal conditions. Radioligand binding and in situ hybridization revealed higher density of CRH-R1 in the amygdala of CRH-COEhom mice under basal conditions compared to control littermates. A significant reduction of the receptor levels was observed in this area after acute stress, suggesting that stress may trigger CRH-R1 internalization/downregulation in these CRH overexpressing mice. Chronic CRH overexpression leads to reduced ERK1/2 activation in response to acute stress in the BLA. © 2009 IBRO. Fil:Silberstein, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Refojo, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03064522_v159_n2_p610_Silberstein
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic CRF
CRH
CRH receptor
ERK
HPA axis
mitogen activated protein kinase 1
mitogen activated protein kinase 3
acute stress
amygdaloid nucleus
animal experiment
article
brain region
controlled study
immunohistochemistry
in situ hybridization
mouse
nonhuman
priority journal
protein expression
Amphibian Proteins
Amygdala
Animals
Autoradiography
Corticosterone
Corticotropin-Releasing Hormone
Disease Models, Animal
Gene Expression Regulation, Enzymologic
Iodine Isotopes
Male
Mice
Mice, Transgenic
Mitogen-Activated Protein Kinase 3
Peptide Hormones
Protein Binding
Radioimmunoassay
Receptors, Corticotropin-Releasing Hormone
Restraint, Physical
Stress, Psychological
Time Factors
spellingShingle CRF
CRH
CRH receptor
ERK
HPA axis
mitogen activated protein kinase 1
mitogen activated protein kinase 3
acute stress
amygdaloid nucleus
animal experiment
article
brain region
controlled study
immunohistochemistry
in situ hybridization
mouse
nonhuman
priority journal
protein expression
Amphibian Proteins
Amygdala
Animals
Autoradiography
Corticosterone
Corticotropin-Releasing Hormone
Disease Models, Animal
Gene Expression Regulation, Enzymologic
Iodine Isotopes
Male
Mice
Mice, Transgenic
Mitogen-Activated Protein Kinase 3
Peptide Hormones
Protein Binding
Radioimmunoassay
Receptors, Corticotropin-Releasing Hormone
Restraint, Physical
Stress, Psychological
Time Factors
Silberstein, S.
Vogl, A.M.
Refojo, D.
Senin, S.A.
Wurst, W.
Holsboer, F.
Deussing, J.M.
Arzt, E.
Amygdaloid pERK1/2 in corticotropin-releasing hormone overexpressing mice under basal and acute stress conditions
topic_facet CRF
CRH
CRH receptor
ERK
HPA axis
mitogen activated protein kinase 1
mitogen activated protein kinase 3
acute stress
amygdaloid nucleus
animal experiment
article
brain region
controlled study
immunohistochemistry
in situ hybridization
mouse
nonhuman
priority journal
protein expression
Amphibian Proteins
Amygdala
Animals
Autoradiography
Corticosterone
Corticotropin-Releasing Hormone
Disease Models, Animal
Gene Expression Regulation, Enzymologic
Iodine Isotopes
Male
Mice
Mice, Transgenic
Mitogen-Activated Protein Kinase 3
Peptide Hormones
Protein Binding
Radioimmunoassay
Receptors, Corticotropin-Releasing Hormone
Restraint, Physical
Stress, Psychological
Time Factors
description Corticotropin-releasing hormone (CRH) coordinates neuroendocrine and behavioral adaptations to stress. Acute CRH administration in vivo activates extracellular signal-regulated kinase 1/2 (ERK1/2) in limbic brain areas, acting through the CRH receptor type 1 (CRH-R1). In the present study, we used CRH-COE-Cam mice that overexpress CRH in limbic-restricted areas, to analyze the effect of chronic CRH overexpression on ERK1/2 activation. By immunohistochemistry and confocal microscopy analysis we found that pERK1/2 levels in the basolateral amygdala (BLA) were similar in control and CRH overexpressing mice under basal conditions. Acute stress caused comparably increased levels of corticosterone in both control (CRH-COEcon-Cam) and CRH overexpressing (CRH-COEhom-Cam) animals. CRH-COEhom-Cam mice after stress showed reduced pERK1/2 immunoreactivity in the BLA compared to CRH-COEhom-Cam animals under basal conditions. Radioligand binding and in situ hybridization revealed higher density of CRH-R1 in the amygdala of CRH-COEhom mice under basal conditions compared to control littermates. A significant reduction of the receptor levels was observed in this area after acute stress, suggesting that stress may trigger CRH-R1 internalization/downregulation in these CRH overexpressing mice. Chronic CRH overexpression leads to reduced ERK1/2 activation in response to acute stress in the BLA. © 2009 IBRO.
format JOUR
author Silberstein, S.
Vogl, A.M.
Refojo, D.
Senin, S.A.
Wurst, W.
Holsboer, F.
Deussing, J.M.
Arzt, E.
author_facet Silberstein, S.
Vogl, A.M.
Refojo, D.
Senin, S.A.
Wurst, W.
Holsboer, F.
Deussing, J.M.
Arzt, E.
author_sort Silberstein, S.
title Amygdaloid pERK1/2 in corticotropin-releasing hormone overexpressing mice under basal and acute stress conditions
title_short Amygdaloid pERK1/2 in corticotropin-releasing hormone overexpressing mice under basal and acute stress conditions
title_full Amygdaloid pERK1/2 in corticotropin-releasing hormone overexpressing mice under basal and acute stress conditions
title_fullStr Amygdaloid pERK1/2 in corticotropin-releasing hormone overexpressing mice under basal and acute stress conditions
title_full_unstemmed Amygdaloid pERK1/2 in corticotropin-releasing hormone overexpressing mice under basal and acute stress conditions
title_sort amygdaloid perk1/2 in corticotropin-releasing hormone overexpressing mice under basal and acute stress conditions
url http://hdl.handle.net/20.500.12110/paper_03064522_v159_n2_p610_Silberstein
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