Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actions

Bibliographic Details
Main Author: Uchoa, Ernane Torres
Publication Date: 2014
Other Authors: Aguilera, Greti, Herman, James P., Fiedler, Jenny L., Deak, Terrence, Sousa, Maria Bernardete Cordeiro de
Format: Article
Language: eng
Source: Repositório Institucional da UFRN
dARK ID: ark:/41046/001300000wbn4
Download full: https://repositorio.ufrn.br/jspui/handle/123456789/23268
Summary: Normal hypothalamic-pituitary-adrenal (HPA) axis activity leading to rhythmic and episodic release of adrenal glucocorticoids is essential for body homeostasis and survival during stress. Acting through specific intracellular receptors in the brain and periphery, glucocorticoids regulate behavior, metabolic, cardiovascular, immune, and neuroendocrine activities. In contrast to chronic elevated levels, circadian and acute stress-induced increases in glucocorticoids are necessary for hippocampal neuronal survival and memory acquisition and consolidation, through inhibiting apoptosis, facilitating glutamate transmission and inducing immediate early genes and spine formation. In addition to its metabolic actions leading to increasing energy availability, glucocorticoids have profound effects on feeding behavior, mainly through modulation of orexigenic and anorixegenic neuropeptides. Evidence is also emerging that in addition to the recognized immune suppressive actions of glucocorticoids by counteracting adrenergic proinflammatory actions, circadian elevations have priming effects in the immune system, potentiating acute defensive responses. In addition, negative feedback by glucocorticoids involves multiple mechanisms leading to limiting HPA axis activation and preventing deleterious effects of excessive glucocorticoid production. Adequate glucocorticoid secretion to meet body demands is tightly regulated by a complex neural circuitry controlling hypothalamic corticotrophin releasing hormone (CRH) and vasopressin secretion, the main regulators of pituitary adrenocorticotrophic hormone (ACTH). Rapid feedback mechanisms, likely involving non-genomic actions of glucocorticoids, mediate immediate inhibition of hypothalamic CRH and ACTH secretion, while intermediate and delayed mechanisms mediated by genomic actions involve modulation of limbic circuitry and peripheral metabolic messengers. Consistent with their key adaptive roles, HPA axis components are evolutionarily conserved, being present in the earliest vertebrates. Understanding these basic mechanisms may lead to novel approaches for the development of diagnostic and therapeutic tools for disorders related to stress and alterations of glucocorticoid secretion.
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spelling Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actionsCRHACTHglucocorticoidscortisol/corticosteroneNormal hypothalamic-pituitary-adrenal (HPA) axis activity leading to rhythmic and episodic release of adrenal glucocorticoids is essential for body homeostasis and survival during stress. Acting through specific intracellular receptors in the brain and periphery, glucocorticoids regulate behavior, metabolic, cardiovascular, immune, and neuroendocrine activities. In contrast to chronic elevated levels, circadian and acute stress-induced increases in glucocorticoids are necessary for hippocampal neuronal survival and memory acquisition and consolidation, through inhibiting apoptosis, facilitating glutamate transmission and inducing immediate early genes and spine formation. In addition to its metabolic actions leading to increasing energy availability, glucocorticoids have profound effects on feeding behavior, mainly through modulation of orexigenic and anorixegenic neuropeptides. Evidence is also emerging that in addition to the recognized immune suppressive actions of glucocorticoids by counteracting adrenergic proinflammatory actions, circadian elevations have priming effects in the immune system, potentiating acute defensive responses. In addition, negative feedback by glucocorticoids involves multiple mechanisms leading to limiting HPA axis activation and preventing deleterious effects of excessive glucocorticoid production. Adequate glucocorticoid secretion to meet body demands is tightly regulated by a complex neural circuitry controlling hypothalamic corticotrophin releasing hormone (CRH) and vasopressin secretion, the main regulators of pituitary adrenocorticotrophic hormone (ACTH). Rapid feedback mechanisms, likely involving non-genomic actions of glucocorticoids, mediate immediate inhibition of hypothalamic CRH and ACTH secretion, while intermediate and delayed mechanisms mediated by genomic actions involve modulation of limbic circuitry and peripheral metabolic messengers. Consistent with their key adaptive roles, HPA axis components are evolutionarily conserved, being present in the earliest vertebrates. Understanding these basic mechanisms may lead to novel approaches for the development of diagnostic and therapeutic tools for disorders related to stress and alterations of glucocorticoid secretion.2017-05-31T12:49:47Z2017-05-31T12:49:47Z2014-09info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://repositorio.ufrn.br/jspui/handle/123456789/2326810.1111/jne.12157ark:/41046/001300000wbn4engUchoa, Ernane TorresAguilera, GretiHerman, James P.Fiedler, Jenny L.Deak, TerrenceSousa, Maria Bernardete Cordeiro deinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRN2022-10-18T22:00:03Zoai:repositorio.ufrn.br:123456789/23268Repositório InstitucionalPUBhttp://repositorio.ufrn.br/oai/repositorio@bczm.ufrn.bropendoar:2022-10-18T22:00:03Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.none.fl_str_mv Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actions
title Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actions
spellingShingle Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actions
Uchoa, Ernane Torres
CRH
ACTH
glucocorticoids
cortisol/corticosterone
title_short Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actions
title_full Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actions
title_fullStr Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actions
title_full_unstemmed Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actions
title_sort Novel aspects of hypothalamic-pituitary-adrenal axis regulation and glucocorticoid actions
author Uchoa, Ernane Torres
author_facet Uchoa, Ernane Torres
Aguilera, Greti
Herman, James P.
Fiedler, Jenny L.
Deak, Terrence
Sousa, Maria Bernardete Cordeiro de
author_role author
author2 Aguilera, Greti
Herman, James P.
Fiedler, Jenny L.
Deak, Terrence
Sousa, Maria Bernardete Cordeiro de
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Uchoa, Ernane Torres
Aguilera, Greti
Herman, James P.
Fiedler, Jenny L.
Deak, Terrence
Sousa, Maria Bernardete Cordeiro de
dc.subject.por.fl_str_mv CRH
ACTH
glucocorticoids
cortisol/corticosterone
topic CRH
ACTH
glucocorticoids
cortisol/corticosterone
description Normal hypothalamic-pituitary-adrenal (HPA) axis activity leading to rhythmic and episodic release of adrenal glucocorticoids is essential for body homeostasis and survival during stress. Acting through specific intracellular receptors in the brain and periphery, glucocorticoids regulate behavior, metabolic, cardiovascular, immune, and neuroendocrine activities. In contrast to chronic elevated levels, circadian and acute stress-induced increases in glucocorticoids are necessary for hippocampal neuronal survival and memory acquisition and consolidation, through inhibiting apoptosis, facilitating glutamate transmission and inducing immediate early genes and spine formation. In addition to its metabolic actions leading to increasing energy availability, glucocorticoids have profound effects on feeding behavior, mainly through modulation of orexigenic and anorixegenic neuropeptides. Evidence is also emerging that in addition to the recognized immune suppressive actions of glucocorticoids by counteracting adrenergic proinflammatory actions, circadian elevations have priming effects in the immune system, potentiating acute defensive responses. In addition, negative feedback by glucocorticoids involves multiple mechanisms leading to limiting HPA axis activation and preventing deleterious effects of excessive glucocorticoid production. Adequate glucocorticoid secretion to meet body demands is tightly regulated by a complex neural circuitry controlling hypothalamic corticotrophin releasing hormone (CRH) and vasopressin secretion, the main regulators of pituitary adrenocorticotrophic hormone (ACTH). Rapid feedback mechanisms, likely involving non-genomic actions of glucocorticoids, mediate immediate inhibition of hypothalamic CRH and ACTH secretion, while intermediate and delayed mechanisms mediated by genomic actions involve modulation of limbic circuitry and peripheral metabolic messengers. Consistent with their key adaptive roles, HPA axis components are evolutionarily conserved, being present in the earliest vertebrates. Understanding these basic mechanisms may lead to novel approaches for the development of diagnostic and therapeutic tools for disorders related to stress and alterations of glucocorticoid secretion.
publishDate 2014
dc.date.none.fl_str_mv 2014-09
2017-05-31T12:49:47Z
2017-05-31T12:49:47Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/jspui/handle/123456789/23268
10.1111/jne.12157
dc.identifier.dark.fl_str_mv ark:/41046/001300000wbn4
url https://repositorio.ufrn.br/jspui/handle/123456789/23268
identifier_str_mv 10.1111/jne.12157
ark:/41046/001300000wbn4
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRN
instname:Universidade Federal do Rio Grande do Norte (UFRN)
instacron:UFRN
instname_str Universidade Federal do Rio Grande do Norte (UFRN)
instacron_str UFRN
institution UFRN
reponame_str Repositório Institucional da UFRN
collection Repositório Institucional da UFRN
repository.name.fl_str_mv Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)
repository.mail.fl_str_mv repositorio@bczm.ufrn.br
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