Sex-dependent effects of acute stress and alcohol exposure during adolescence on mRNA expression of brain signaling systems involved in reward and stress responses in young adult rats.


Journal

Biology of sex differences
ISSN: 2042-6410
Titre abrégé: Biol Sex Differ
Pays: England
ID NLM: 101548963

Informations de publication

Date de publication:
26 Sep 2024
Historique:
received: 12 06 2024
accepted: 09 09 2024
medline: 27 9 2024
pubmed: 27 9 2024
entrez: 26 9 2024
Statut: epublish

Résumé

Adolescent stress and alcohol exposure increase the risk of maladaptive behaviors and mental disorders in adulthood, with distinct sex-specific differences. Understanding the mechanisms underlying these early events is crucial for developing targeted prevention and treatment strategies. Male and female Wistar rats were exposed to acute restraint stress and intermittent alcohol during adolescence. We assessed lasting effects on plasma corticosterone (CORT) and adrenocorticotropic hormone (ACTH) levels, and mRNA expression of genes related to corticotropin releasing hormone (CRH), neuropeptide Y (NPY), corticoid, opioid, and arginine vasopressin systems in the amygdala and hypothalamus. The main findings are as follows: (1) blood alcohol concentrations (BAC) increased after the final alcohol administration, but stressed males had lower BAC than non-stressed males; (2) Males gained significantly more weight than females; (3) Stressed females showed higher ACTH levels than non-stressed females, with no changes in males; (4) Stress increased CORT levels in males, while stressed, alcohol-treated females had lower CORT levels than non-stressed females; (5) CRH: Females had lower Crhr1 levels in the amygdala, while alcohol reduced Crhr2 levels in males but not females. Significant interactions among sex, stress, and alcohol were found in the hypothalamus, with distinct patterns between sexes; (6) NPY: In the amygdala, stress reduced Npy and Npy1r levels in males but increased them in females. Alcohol decreased Npy2r levels in males, with varied effects in females. Similar sex-specific patterns were observed in the hypothalamus; (7) Corticoid system: Stress and alcohol had complex, sex-dependent effects on Pomc, Nr3c1, and Nr3c2 in both brain regions; (8) Opioid receptors: Stress and alcohol blunted the elevated expression of Oprm1, Oprd1, and Oprk1 in the amygdala of males and the hypothalamus of females; (8) Vasopressin: Stress and alcohol interacted significantly to affect Avp and Avpr1a expression in the amygdala, with stronger effects in females. In the hypothalamus, alcohol increased Avp levels in females. This study demonstrates that adolescent acute stress and alcohol exposure induce lasting, sex-specific alterations in systems involved in reward and stress responses. These findings emphasize the importance of considering sex differences in the prevention and management of HPA dysfunction and psychiatric disorders.

Sections du résumé

BACKGROUND BACKGROUND
Adolescent stress and alcohol exposure increase the risk of maladaptive behaviors and mental disorders in adulthood, with distinct sex-specific differences. Understanding the mechanisms underlying these early events is crucial for developing targeted prevention and treatment strategies.
METHODS METHODS
Male and female Wistar rats were exposed to acute restraint stress and intermittent alcohol during adolescence. We assessed lasting effects on plasma corticosterone (CORT) and adrenocorticotropic hormone (ACTH) levels, and mRNA expression of genes related to corticotropin releasing hormone (CRH), neuropeptide Y (NPY), corticoid, opioid, and arginine vasopressin systems in the amygdala and hypothalamus.
RESULTS RESULTS
The main findings are as follows: (1) blood alcohol concentrations (BAC) increased after the final alcohol administration, but stressed males had lower BAC than non-stressed males; (2) Males gained significantly more weight than females; (3) Stressed females showed higher ACTH levels than non-stressed females, with no changes in males; (4) Stress increased CORT levels in males, while stressed, alcohol-treated females had lower CORT levels than non-stressed females; (5) CRH: Females had lower Crhr1 levels in the amygdala, while alcohol reduced Crhr2 levels in males but not females. Significant interactions among sex, stress, and alcohol were found in the hypothalamus, with distinct patterns between sexes; (6) NPY: In the amygdala, stress reduced Npy and Npy1r levels in males but increased them in females. Alcohol decreased Npy2r levels in males, with varied effects in females. Similar sex-specific patterns were observed in the hypothalamus; (7) Corticoid system: Stress and alcohol had complex, sex-dependent effects on Pomc, Nr3c1, and Nr3c2 in both brain regions; (8) Opioid receptors: Stress and alcohol blunted the elevated expression of Oprm1, Oprd1, and Oprk1 in the amygdala of males and the hypothalamus of females; (8) Vasopressin: Stress and alcohol interacted significantly to affect Avp and Avpr1a expression in the amygdala, with stronger effects in females. In the hypothalamus, alcohol increased Avp levels in females.
CONCLUSIONS CONCLUSIONS
This study demonstrates that adolescent acute stress and alcohol exposure induce lasting, sex-specific alterations in systems involved in reward and stress responses. These findings emphasize the importance of considering sex differences in the prevention and management of HPA dysfunction and psychiatric disorders.

Identifiants

pubmed: 39327618
doi: 10.1186/s13293-024-00649-5
pii: 10.1186/s13293-024-00649-5
doi:

Substances chimiques

RNA, Messenger 0
Ethanol 3K9958V90M
Neuropeptide Y 0
Corticosterone W980KJ009P
Adrenocorticotropic Hormone 9002-60-2
Corticotropin-Releasing Hormone 9015-71-8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

75

Subventions

Organisme : Instituto de Salud Carlos III (ISCIII), Ministerio de Ciencia e Innovación and European Regional Development Funds-European Union (ERDF-EU)
ID : PI19/00886, PI20/01399, PI22/00427 and PI22/01833
Organisme : Instituto de Salud Carlos III (ISCIII), Ministerio de Ciencia e Innovación and European Regional Development Funds-European Union (ERDF-EU)
ID : PI19/00886, PI20/01399, PI22/00427 and PI22/01833
Organisme : Instituto de Salud Carlos III (ISCIII), Ministerio de Ciencia e Innovación and European Regional Development Funds-European Union (ERDF-EU)
ID : PI19/00886, PI20/01399, PI22/00427 and PI22/01833
Organisme : Plataforma de biobanco y biomodelos animales y 3D de Málaga
ID : PT20-00101
Organisme : Plataforma de biobanco y biomodelos animales y 3D de Málaga
ID : PT20-00101
Organisme : Programa RICORS RIAPAD
ID : RD21/0009/0003
Organisme : Programa RICORS RIAPAD
ID : RD21/0009/0003
Organisme : Ministerio de Sanidad, Delegación de Gobierno para el Plan Nacional sobre Drogas
ID : PNSD 2022/020

Informations de copyright

© 2024. The Author(s).

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Auteurs

Carlotta Gobbi (C)

Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA- Plataforma BIONAND), Málaga, 29590, Spain.
Unidad de Gestión Clínica de Salud Mental, Hospital Regional Universitario de Málaga, Málaga, 29010, Spain.

Laura Sánchez-Marín (L)

Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA- Plataforma BIONAND), Málaga, 29590, Spain.
Unidad de Gestión Clínica de Salud Mental, Hospital Regional Universitario de Málaga, Málaga, 29010, Spain.

María Flores-López (M)

Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA- Plataforma BIONAND), Málaga, 29590, Spain.
Unidad de Gestión Clínica de Salud Mental, Hospital Regional Universitario de Málaga, Málaga, 29010, Spain.

Dina Medina-Vera (D)

Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA- Plataforma BIONAND), Málaga, 29590, Spain.
Unidad Clínica Área del Corazón, Hospital Universitario Virgen de la Victoria de Málaga, Málaga, 29010, Spain.

Francisco Javier Pavón-Morón (FJ)

Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA- Plataforma BIONAND), Málaga, 29590, Spain. javier.pavon@ibima.eu.
Unidad Clínica Área del Corazón, Hospital Universitario Virgen de la Victoria de Málaga, Málaga, 29010, Spain. javier.pavon@ibima.eu.
Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), Instituto de Salud Carlos III, Madrid, 28029, Spain. javier.pavon@ibima.eu.

Fernando Rodríguez de Fonseca (F)

Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA- Plataforma BIONAND), Málaga, 29590, Spain. fernando.rodriguez@ibima.eu.
Unidad de Gestión Clínica de Neurología, Hospital Regional Universitario de Málaga, Málaga, 29010, Spain. fernando.rodriguez@ibima.eu.

Antonia Serrano (A)

Instituto de Investigación Biomédica de Málaga y Plataforma en Nanomedicina (IBIMA- Plataforma BIONAND), Málaga, 29590, Spain.
Unidad de Gestión Clínica de Salud Mental, Hospital Regional Universitario de Málaga, Málaga, 29010, Spain.

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