Mirabegron relaxes arteries from human visceral adipose tissue through antagonism of α


Journal

Vascular pharmacology
ISSN: 1879-3649
Titre abrégé: Vascul Pharmacol
Pays: United States
ID NLM: 101130615

Informations de publication

Date de publication:
10 2022
Historique:
received: 03 05 2022
revised: 13 07 2022
accepted: 02 08 2022
pubmed: 8 8 2022
medline: 14 10 2022
entrez: 7 8 2022
Statut: ppublish

Résumé

As inadequate perfusion has emerged as a key determinant of adipose tissue dysfunction in obesity, interest has grown regarding possible pharmacological interventions to prevent this process. Mirabegron has proved to improve insulin sensitivity and glucose homeostasis in obese humans via stimulation of β Small arteries (116-734 μm) isolated from visceral adipose tissue were studied ex vivo in a wire myograph. After vessels had been contracted, changes in vascular tone in response to mirabegron were determined under different conditions. Mirabegron did not elicit vasorelaxation in vessels contracted with U46619 or high-K Mirabegron induces endothelium-independent vasorelaxation in arteries from visceral adipose tissue, likely through antagonism of α

Identifiants

pubmed: 35934296
pii: S1537-1891(22)00143-4
doi: 10.1016/j.vph.2022.107094
pii:
doi:

Substances chimiques

Acetanilides 0
Adrenergic Agonists 0
Receptors, Adrenergic, alpha-1 0
Thiazoles 0
Phenylephrine 1WS297W6MV
15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid 76898-47-0
Glucose IY9XDZ35W2
mirabegron MVR3JL3B2V

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

107094

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Alessandro De Stefano (A)

Department of Systems Medicine, Tor Vergata University, Roma, Italy.

Francesca Schinzari (F)

Department of Aging, Policlinico A. Gemelli IRCCS, Roma, Italy.

Nicola Di Daniele (N)

Department of Systems Medicine, Tor Vergata University, Roma, Italy.

Giuseppe Sica (G)

Department of Experimental Medicine and Surgery, Tor Vergata University, Roma, Italy.

Paolo Gentileschi (P)

Department of Experimental Medicine and Surgery, Tor Vergata University, Roma, Italy.

Giuseppina Vizioli (G)

Department of Translational Medicine and Surgery, Catholic University, Rome, Italy.

Carmine Cardillo (C)

Department of Aging, Policlinico A. Gemelli IRCCS, Roma, Italy; Department of Translational Medicine and Surgery, Catholic University, Rome, Italy. Electronic address: carmine.cardillo@unicatt.it.

Manfredi Tesauro (M)

Department of Systems Medicine, Tor Vergata University, Roma, Italy.

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Classifications MeSH