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A comparative study of human and zebrafish glucocorticoid receptor activities of natural and pharmaceutical steroids.
Toso, Anna; Boulahtouf, Abdelhay; Escande, Aurélie; Garoche, Clémentine; Balaguer, Patrick.
Afiliação
  • Toso A; Institut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U1194, Université Montpellier, Institut Régional du Cancer de Montpellier (ICM), Montpellier, France.
  • Boulahtouf A; Institut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U1194, Université Montpellier, Institut Régional du Cancer de Montpellier (ICM), Montpellier, France.
  • Escande A; UMR Hydrosciences Montpellier, Université de Montpellier, Montpellier, France.
  • Garoche C; Institut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U1194, Université Montpellier, Institut Régional du Cancer de Montpellier (ICM), Montpellier, France.
  • Balaguer P; Institut de Recherche en Cancérologie de Montpellier (IRCM), Inserm U1194, Université Montpellier, Institut Régional du Cancer de Montpellier (ICM), Montpellier, France.
Front Endocrinol (Lausanne) ; 14: 1235501, 2023.
Article em En | MEDLINE | ID: mdl-37654569
ABSTRACT

Introduction:

The action of environmental steroids on the human glucocorticoid receptor (hGR) has been pointed out with the risk to impair physiological immune and metabolic processes regulated by this nuclear receptor. However, there is still a lack of mechanistic information regarding their ability to interact with GR in aquatic species.

Methods:

To investigate ligand activation differences between hGR and zebrafish GR (zfGR), we tested several natural and synthetic steroids using reporter cell lines expressing hGR or zfGR. Results and

discussion:

Almost all the glucocorticoids tested (dexamethasone, cortisol, bimedrazol, medrol, cortivazol and fluticasone) are agonists of the two receptors with similar potencies. The dissociated glucocorticoids, RU24782 and RU24858 are agonists of both zfGR and hGR but with a better potency for the latter. On the other hand, the synthetic glucocorticoid forbimenol and the mineralocorticoid aldosterone are agonist on hGR but antagonist on zfGR. The other steroids tested, androgens and progestins, are all antagonists of both GRs with equal or lower potency on zfGR than on hGR. Surprisingly, the lower efficacy and potency on zfGR of aldosterone, forbimenol and the dissociated glucocorticoids is not related to their affinity for the receptors which would suggest that it could be related to less efficacious recruitment of coactivators by zfGR compared to hGR.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Glucocorticoides / Glucocorticoides Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Glucocorticoides / Glucocorticoides Limite: Animals / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article