Cargando…

Evaluation of the HPA Axis’ Response to Pharmacological Challenges in Experimental and Clinical Early-Life Stress-Associated Depression

Early-life stress (ELS) is associated with a higher risk of psychopathologies in adulthood, such as depression, which may be related to persistent changes in the hypothalamic-pituitary-adrenal (HPA) axis. This study aimed to evaluate the effects of ELS on the functioning of the HPA axis in clinical...

Descripción completa

Detalles Bibliográficos
Autores principales: Barroca, Nayara Cobra Barreiro, Baes, Cristiane Von Werne, Martins-Monteverde, Camila Maria Severi, Bosaipo, Nayanne Beckmann, Santos da Silva Umeoka, Marcia, Tejada, Julian, Antunes-Rodrigues, José, de Castro, Margaret, Juruena, Mario Francisco, Garcia-Cairasco, Norberto, Umeoka, Eduardo Henrique de Lima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814478/
https://www.ncbi.nlm.nih.gov/pubmed/33318074
http://dx.doi.org/10.1523/ENEURO.0222-20.2020
_version_ 1783638062484422656
author Barroca, Nayara Cobra Barreiro
Baes, Cristiane Von Werne
Martins-Monteverde, Camila Maria Severi
Bosaipo, Nayanne Beckmann
Santos da Silva Umeoka, Marcia
Tejada, Julian
Antunes-Rodrigues, José
de Castro, Margaret
Juruena, Mario Francisco
Garcia-Cairasco, Norberto
Umeoka, Eduardo Henrique de Lima
author_facet Barroca, Nayara Cobra Barreiro
Baes, Cristiane Von Werne
Martins-Monteverde, Camila Maria Severi
Bosaipo, Nayanne Beckmann
Santos da Silva Umeoka, Marcia
Tejada, Julian
Antunes-Rodrigues, José
de Castro, Margaret
Juruena, Mario Francisco
Garcia-Cairasco, Norberto
Umeoka, Eduardo Henrique de Lima
author_sort Barroca, Nayara Cobra Barreiro
collection PubMed
description Early-life stress (ELS) is associated with a higher risk of psychopathologies in adulthood, such as depression, which may be related to persistent changes in the hypothalamic-pituitary-adrenal (HPA) axis. This study aimed to evaluate the effects of ELS on the functioning of the HPA axis in clinical and experimental situations. Clinically, patients with current depressive episodes, with and without ELS, and healthy controls, composed the sample. Subjects took a capsule containing placebo, fludrocortisone, prednisolone, dexamethasone or spironolactone followed by an assessment of plasma cortisol the morning after. Experimentally, male Wistar rats were submitted to ELS protocol based on variable, unpredictable stressors from postnatal day (PND)1 to PND21. On PND65 animals were behaviorally evaluated through the forced-swimming test (FST). At PND68, pharmacological challenges started, using mifepristone, dexamethasone, spironolactone, or fludrocortisone, and corticosterone levels were determined 3 h after injections. Cortisol response of the patients did not differ significantly from healthy subjects, regardless of their ELS history, and it was lower after fludrocortisone, prednisolone, and dexamethasone compared with placebo, indicating the suppression of plasma cortisol by all these treatments. Animals exposed to ELS presented altered phenotype as indicated by an increased immobility time in the FST when compared with control, but no significant long-lasting effects of ELS were observed on the HPA axis response. Limitations on the way the volunteers were sampled may have contributed to the lack of ELS effects on the HPA axis, pointing out the need for further research to understand these complex phenomena
format Online
Article
Text
id pubmed-7814478
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Society for Neuroscience
record_format MEDLINE/PubMed
spelling pubmed-78144782021-01-21 Evaluation of the HPA Axis’ Response to Pharmacological Challenges in Experimental and Clinical Early-Life Stress-Associated Depression Barroca, Nayara Cobra Barreiro Baes, Cristiane Von Werne Martins-Monteverde, Camila Maria Severi Bosaipo, Nayanne Beckmann Santos da Silva Umeoka, Marcia Tejada, Julian Antunes-Rodrigues, José de Castro, Margaret Juruena, Mario Francisco Garcia-Cairasco, Norberto Umeoka, Eduardo Henrique de Lima eNeuro Research Article: Negative Results Early-life stress (ELS) is associated with a higher risk of psychopathologies in adulthood, such as depression, which may be related to persistent changes in the hypothalamic-pituitary-adrenal (HPA) axis. This study aimed to evaluate the effects of ELS on the functioning of the HPA axis in clinical and experimental situations. Clinically, patients with current depressive episodes, with and without ELS, and healthy controls, composed the sample. Subjects took a capsule containing placebo, fludrocortisone, prednisolone, dexamethasone or spironolactone followed by an assessment of plasma cortisol the morning after. Experimentally, male Wistar rats were submitted to ELS protocol based on variable, unpredictable stressors from postnatal day (PND)1 to PND21. On PND65 animals were behaviorally evaluated through the forced-swimming test (FST). At PND68, pharmacological challenges started, using mifepristone, dexamethasone, spironolactone, or fludrocortisone, and corticosterone levels were determined 3 h after injections. Cortisol response of the patients did not differ significantly from healthy subjects, regardless of their ELS history, and it was lower after fludrocortisone, prednisolone, and dexamethasone compared with placebo, indicating the suppression of plasma cortisol by all these treatments. Animals exposed to ELS presented altered phenotype as indicated by an increased immobility time in the FST when compared with control, but no significant long-lasting effects of ELS were observed on the HPA axis response. Limitations on the way the volunteers were sampled may have contributed to the lack of ELS effects on the HPA axis, pointing out the need for further research to understand these complex phenomena Society for Neuroscience 2021-01-13 /pmc/articles/PMC7814478/ /pubmed/33318074 http://dx.doi.org/10.1523/ENEURO.0222-20.2020 Text en Copyright © 2021 Barroca et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: Negative Results
Barroca, Nayara Cobra Barreiro
Baes, Cristiane Von Werne
Martins-Monteverde, Camila Maria Severi
Bosaipo, Nayanne Beckmann
Santos da Silva Umeoka, Marcia
Tejada, Julian
Antunes-Rodrigues, José
de Castro, Margaret
Juruena, Mario Francisco
Garcia-Cairasco, Norberto
Umeoka, Eduardo Henrique de Lima
Evaluation of the HPA Axis’ Response to Pharmacological Challenges in Experimental and Clinical Early-Life Stress-Associated Depression
title Evaluation of the HPA Axis’ Response to Pharmacological Challenges in Experimental and Clinical Early-Life Stress-Associated Depression
title_full Evaluation of the HPA Axis’ Response to Pharmacological Challenges in Experimental and Clinical Early-Life Stress-Associated Depression
title_fullStr Evaluation of the HPA Axis’ Response to Pharmacological Challenges in Experimental and Clinical Early-Life Stress-Associated Depression
title_full_unstemmed Evaluation of the HPA Axis’ Response to Pharmacological Challenges in Experimental and Clinical Early-Life Stress-Associated Depression
title_short Evaluation of the HPA Axis’ Response to Pharmacological Challenges in Experimental and Clinical Early-Life Stress-Associated Depression
title_sort evaluation of the hpa axis’ response to pharmacological challenges in experimental and clinical early-life stress-associated depression
topic Research Article: Negative Results
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814478/
https://www.ncbi.nlm.nih.gov/pubmed/33318074
http://dx.doi.org/10.1523/ENEURO.0222-20.2020
work_keys_str_mv AT barrocanayaracobrabarreiro evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT baescristianevonwerne evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT martinsmonteverdecamilamariaseveri evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT bosaiponayannebeckmann evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT santosdasilvaumeokamarcia evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT tejadajulian evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT antunesrodriguesjose evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT decastromargaret evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT juruenamariofrancisco evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT garciacairasconorberto evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression
AT umeokaeduardohenriquedelima evaluationofthehpaaxisresponsetopharmacologicalchallengesinexperimentalandclinicalearlylifestressassociateddepression