Progesterone: An enigmatic ligand for the mineralocorticoid receptor.


Journal

Biochemical pharmacology
ISSN: 1873-2968
Titre abrégé: Biochem Pharmacol
Pays: England
ID NLM: 0101032

Informations de publication

Date de publication:
07 2020
Historique:
received: 20 01 2020
accepted: 10 04 2020
pubmed: 20 4 2020
medline: 2 12 2020
entrez: 20 4 2020
Statut: ppublish

Résumé

The progesterone receptor (PR) mediates progesterone regulation of female reproductive physiology, as well as gene transcription in non-reproductive tissues, such as brain, bone, lung and vasculature, in both women and men. An unusual property of progesterone is its high affinity for the mineralocorticoid receptor (MR), which regulates electrolyte transport in the kidney in humans and other terrestrial vertebrates. In humans, rats, alligators and frogs, progesterone antagonizes activation of the MR by aldosterone, the physiological mineralocorticoid in terrestrial vertebrates. In contrast, in elephant shark, ray-finned fishes and chickens, progesterone activates the MR. Interestingly, cartilaginous fishes and ray-finned fishes do not synthesize aldosterone, raising the question of which steroid(s) activate the MR in cartilaginous fishes and ray-finned fishes. The simpler synthesis of progesterone, compared to cortisol and other corticosteroids, makes progesterone a candidate physiological activator of the MR in elephant sharks and ray-finned fishes. Elephant shark and ray-finned fish MRs are expressed in diverse tissues, including heart, brain and lung, as well as, ovary and testis, two reproductive tissues that are targets for progesterone, which together suggests a multi-faceted physiological role for progesterone activation of the MR in elephant shark and ray-finned fish. The functional consequences of progesterone as an antagonist of some terrestrial vertebrate MRs and as an agonist of fish and chicken MRs are not fully understood. The physiological activities of progesterone through binding to vertebrate MRs merits further investigation.

Identifiants

pubmed: 32305433
pii: S0006-2952(20)30204-5
doi: 10.1016/j.bcp.2020.113976
pii:
doi:

Substances chimiques

Ligands 0
Receptors, Mineralocorticoid 0
Aldosterone 4964P6T9RB
Progesterone 4G7DS2Q64Y
Hydrocortisone WI4X0X7BPJ

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

113976

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Michael E Baker (ME)

Division of Nephrology-Hypertension, Department of Medicine, 0735, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0735, United States. Electronic address: mbaker@ucsd.edu.

Yoshinao Katsu (Y)

Graduate School of Life Science, Hokkaido University, Sapporo, Japan. Electronic address: ykatsu@sci.hokudai.ac.jp.

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Classifications MeSH