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The effect of chronic stress on sensitivity to dexamethasone treatment of HPA axis gene expression in C57Bl/6 mice. / Salman, Rasha; Ritter, Polina; Ryabushkina, Yuliya и др.

в: Behavioural Brain Research, Том 500, 116000, 05.03.2026.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Vancouver

Salman R, Ritter P, Ryabushkina Y, Khantakova J, Bondar N. The effect of chronic stress on sensitivity to dexamethasone treatment of HPA axis gene expression in C57Bl/6 mice. Behavioural Brain Research. 2026 март 5;500:116000. doi: 10.1016/j.bbr.2025.116000

Author

Salman, Rasha ; Ritter, Polina ; Ryabushkina, Yuliya и др. / The effect of chronic stress on sensitivity to dexamethasone treatment of HPA axis gene expression in C57Bl/6 mice. в: Behavioural Brain Research. 2026 ; Том 500.

BibTeX

@article{356b47ef6dbf44c693b6d50fa0c3470b,
title = "The effect of chronic stress on sensitivity to dexamethasone treatment of HPA axis gene expression in C57Bl/6 mice",
abstract = "Chronic social stress is a major risk for psychopathologies such as depression, often leading to altered hypothalamic-pituitary-adrenal (HPA) axis function and glucocorticoid resistance. This study examines how chronic social defeat stress (CSDS) affects sensitivity to dexamethasone by analyzing HPA axis genes expression in C57Bl/6 mice. Adult male mice were subjected to 30 days of stress, followed by dexamethasone or saline administration. Genes expression was analyzed in the hypothalamus, prefrontal cortex (PFC; Nr3c1 only), and adrenal glands at multiple time points post-treatment. CSDS induced marked dysregulation of HPA axis-related genes, including a decrease in hypothalamic Crh and Crhbp, and adrenal Mc2r, Nr3c1, alongside an upregulation of steroidogenic enzymes Cyp11a1 and Cyp11b1, which may account for the elevated corticosterone levels observed under chronic stress conditions. CSDS alters the genes expression response to dexamethasone, indicating a delayed recovery of glucocorticoid receptor signaling in the brain and adrenal glands. Our findings reveal significant stress-induced alterations in the expression of key HPA axis genes, suggesting impaired glucocorticoid receptor signaling and potential glucocorticoid resistance in stressed mice.",
keywords = "C57Bl/6 mice, Chronic social stress, Dexamethasone, Gene expression, Glucocorticoid resistance, HPA axis",
author = "Rasha Salman and Polina Ritter and Yuliya Ryabushkina and Julia Khantakova and Natalya Bondar",
note = "This study was supported by FWNR-2022–0166 (Russia).",
year = "2026",
month = mar,
day = "5",
doi = "10.1016/j.bbr.2025.116000",
language = "English",
volume = "500",
journal = "Behavioural Brain Research",
issn = "0166-4328",
publisher = "Elsevier Science Publishing Company, Inc.",

}

RIS

TY - JOUR

T1 - The effect of chronic stress on sensitivity to dexamethasone treatment of HPA axis gene expression in C57Bl/6 mice

AU - Salman, Rasha

AU - Ritter, Polina

AU - Ryabushkina, Yuliya

AU - Khantakova, Julia

AU - Bondar, Natalya

N1 - This study was supported by FWNR-2022–0166 (Russia).

PY - 2026/3/5

Y1 - 2026/3/5

N2 - Chronic social stress is a major risk for psychopathologies such as depression, often leading to altered hypothalamic-pituitary-adrenal (HPA) axis function and glucocorticoid resistance. This study examines how chronic social defeat stress (CSDS) affects sensitivity to dexamethasone by analyzing HPA axis genes expression in C57Bl/6 mice. Adult male mice were subjected to 30 days of stress, followed by dexamethasone or saline administration. Genes expression was analyzed in the hypothalamus, prefrontal cortex (PFC; Nr3c1 only), and adrenal glands at multiple time points post-treatment. CSDS induced marked dysregulation of HPA axis-related genes, including a decrease in hypothalamic Crh and Crhbp, and adrenal Mc2r, Nr3c1, alongside an upregulation of steroidogenic enzymes Cyp11a1 and Cyp11b1, which may account for the elevated corticosterone levels observed under chronic stress conditions. CSDS alters the genes expression response to dexamethasone, indicating a delayed recovery of glucocorticoid receptor signaling in the brain and adrenal glands. Our findings reveal significant stress-induced alterations in the expression of key HPA axis genes, suggesting impaired glucocorticoid receptor signaling and potential glucocorticoid resistance in stressed mice.

AB - Chronic social stress is a major risk for psychopathologies such as depression, often leading to altered hypothalamic-pituitary-adrenal (HPA) axis function and glucocorticoid resistance. This study examines how chronic social defeat stress (CSDS) affects sensitivity to dexamethasone by analyzing HPA axis genes expression in C57Bl/6 mice. Adult male mice were subjected to 30 days of stress, followed by dexamethasone or saline administration. Genes expression was analyzed in the hypothalamus, prefrontal cortex (PFC; Nr3c1 only), and adrenal glands at multiple time points post-treatment. CSDS induced marked dysregulation of HPA axis-related genes, including a decrease in hypothalamic Crh and Crhbp, and adrenal Mc2r, Nr3c1, alongside an upregulation of steroidogenic enzymes Cyp11a1 and Cyp11b1, which may account for the elevated corticosterone levels observed under chronic stress conditions. CSDS alters the genes expression response to dexamethasone, indicating a delayed recovery of glucocorticoid receptor signaling in the brain and adrenal glands. Our findings reveal significant stress-induced alterations in the expression of key HPA axis genes, suggesting impaired glucocorticoid receptor signaling and potential glucocorticoid resistance in stressed mice.

KW - C57Bl/6 mice

KW - Chronic social stress

KW - Dexamethasone

KW - Gene expression

KW - Glucocorticoid resistance

KW - HPA axis

UR - https://www.scopus.com/pages/publications/105025139818

UR - https://www.mendeley.com/catalogue/e85e1e68-9ab8-3fc4-8a4b-9f7f35fdefee/

U2 - 10.1016/j.bbr.2025.116000

DO - 10.1016/j.bbr.2025.116000

M3 - Article

C2 - 41412335

VL - 500

JO - Behavioural Brain Research

JF - Behavioural Brain Research

SN - 0166-4328

M1 - 116000

ER -

ID: 72894372