Endocrine disruptors, aryl hydrocarbon receptor and cortisol secretion.

Adrenal cortex Aryl hydrocarbon receptor Cortisol Endocrine disruptor

Journal

Journal of endocrinological investigation
ISSN: 1720-8386
Titre abrégé: J Endocrinol Invest
Pays: Italy
ID NLM: 7806594

Informations de publication

Date de publication:
18 Apr 2024
Historique:
received: 21 12 2023
accepted: 29 03 2024
medline: 19 4 2024
pubmed: 19 4 2024
entrez: 18 4 2024
Statut: aheadofprint

Résumé

Endocrine disruptors exert a plethora of effects in endocrine tissues, from altered function to carcinogenesis. Given its lipophilic nature, the adrenal cortex represents an ideal target for endocrine disruptors and thus, possibly, xenobiotic-induced adrenocortical dysfunction. However, there is no clear understanding of the effect of endocrine disruptors on adrenal steroidogenesis, in particular as regards the aryl hydrocarbon receptor (AHR) pathway, one of the key mediators. The present review recapitulates available evidence on the effects of AHR ligands on adrenal steroidogenesis, with focus on cortisol secretion. Short-term exposure to AHR ligands most often induced a stress-like corticosteroid response followed by decreased responsiveness to stressors with long-term exposure. This was observed in several experimental models across species as well as in animals and humans in real-life settings. Prenatal exposure led to different effects according to sex of the offspring, as observed in murine models and in children from mothers in several countries. In vitro findings proved highly dependent on the experimental setting, with reduced cortisol response and steroidogenic enzyme synthesis mostly observed in fish and increased cortisol synthesis and secretion observed in murine and human adrenal cell lines. Of note, no AHR-binding element was detected in steroidogenic enzyme promoters, suggesting the involvement of additional factors. Our review provides evidence for the impact of AHR ligands on adrenocortical function and indicates further avenues of research to better clarify its effects.

Identifiants

pubmed: 38637430
doi: 10.1007/s40618-024-02371-w
pii: 10.1007/s40618-024-02371-w
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s).

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Auteurs

F Pecori Giraldi (F)

Department of Clinical Sciences and Community Health, University of Milan, Via Commenda 19, Milan, Italy. francesca.pecorigiraldi@unimi.it.

F Ferraù (F)

Department of Human Pathology of Adulthood and Childhood "Gaetano Barresi,", University of Messina, Messina, Italy.

M Ragonese (M)

Department of Human Pathology of Adulthood and Childhood "Gaetano Barresi,", University of Messina, Messina, Italy.

S Cannavò (S)

Department of Human Pathology of Adulthood and Childhood "Gaetano Barresi,", University of Messina, Messina, Italy.

Classifications MeSH