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Exploration of the Urocontrin a Scaffold Yields New Urotensinergic System Allosteric Modulator and Competitive Antagonists

Billard, Étienne; Hébert, Terence E et Chatenet, David ORCID logoORCID: https://orcid.org/0000-0002-7270-4328 (2023). Exploration of the Urocontrin a Scaffold Yields New Urotensinergic System Allosteric Modulator and Competitive Antagonists Biochemical Pharmacology , vol. 211 , nº 115485. pp. 1-10. DOI: 10.1016/j.bcp.2023.115485.

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Résumé


The urotensinergic system, involved in the development and/or progression of numerous pathological conditions, is composed of one G protein-coupled receptor (UT) and two endogenous ligands known as urotensin II (UII) and urotensin II-related peptide (URP). These two structurally related hormones, which exert common and divergent effects, are thought to play specific biological roles. In recent years, we have characterized an analog termed urocontrin A (UCA), i.e. [Pep(4)]URP, which is capable of discriminating the effects of UII from URP. Such an action could allow the delineation of the respective functions of these two endogenous ligands. In an effort to define the molecular determinants involved in this behavior and to improve the pharmacological profile of UCA, we introduced modifications from urantide, considered for some time as a lead compound for the development of UT antagonists, into UCA and assessed the binding, contractile activity and G protein signaling of these newly developed compounds. Our results show that UCA and its derivatives exert probe-dependent effects on UT antagonism, and we have further identified [Pen(2), Pep(4)]URP as a G(q) biased ligand with an insurmountable antagonism in our aortic ring contraction assay.

Type de document: Article
Mots-clés libres: Aortic ring bioassay; BRET-based biosensor; Biased agonism; Human urotensin II receptor; Probe-dependent action; Urantide; Urocontrin A; Urotensin II-related peptide
Centre: Centre INRS-Institut Armand Frappier
Date de dépôt: 25 juill. 2023 04:05
Dernière modification: 25 juill. 2023 04:05
URI: https://espace.inrs.ca/id/eprint/13348

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