Expression and Impact of Adenosine A(3) Receptors on Calcium Homeostasis in Human Right Atrium

Increased adenosine A(2A) receptor (A(2A)R) expression and activation underlies a higher incidence of spontaneous calcium release in atrial fibrillation (AF). Adenosine A(3) receptors (A(3)R) could counteract excessive A(2A)R activation, but their functional role in the atrium remains elusive, and w...

Descripción completa

Detalles Bibliográficos
Autores: Tarifa, C, Jimenez-Sabado, V, Franco, R, Montiel, J, Guerra, J, Ciruela, F, Hove-Madsen, L
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2023
País:España
Institución:Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
Repositorio:r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
OAI Identifier:oai:iibsantpau.fundanetsuite.com:p16019
Acceso en línea:https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=16019
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85149844511&doi=10.3390%2fijms24054404&partnerID=40&md5=85ba43cd436eac54854d169a35960e3d
Access Level:acceso abierto
Palabra clave:human atrial myocyte
adenosine A(3) receptor
adenosine A(2A) receptor
sarcoplasmic reticulum
calcium spark
transient inward current
L-type calcium current
electrophysiology
Descripción
Sumario:Increased adenosine A(2A) receptor (A(2A)R) expression and activation underlies a higher incidence of spontaneous calcium release in atrial fibrillation (AF). Adenosine A(3) receptors (A(3)R) could counteract excessive A(2A)R activation, but their functional role in the atrium remains elusive, and we therefore aimed to address the impact of A(3)Rs on intracellular calcium homeostasis. For this purpose, we analyzed right atrial samples or myocytes from 53 patients without AF, using quantitative PCR, patch-clamp technique, immunofluorescent labeling or confocal calcium imaging. A(3)R mRNA accounted for 9% and A(2A)R mRNA for 32%. At baseline, A(3)R inhibition increased the transient inward current (I-TI) frequency from 0.28 to 0.81 events/min (p < 0.05). Simultaneous stimulation of A(2A)Rs and A(3)Rs increased the calcium spark frequency seven-fold (p < 0.001) and the I-TI frequency from 0.14 to 0.64 events/min (p < 0.05). Subsequent A(3)R inhibition caused a strong additional increase in the I-TI frequency (to 2.04 events/min; p < 0.01) and increased phosphorylation at s2808 1.7-fold (p < 0.001). These pharmacological treatments had no significant effects on L-type calcium current density or sarcoplasmic reticulum calcium load. In conclusion, A(3)Rs are expressed and blunt spontaneous calcium release at baseline and upon A(2A)R-stimulation in human atrial myocytes, pointing to A(3)R activation as a means to attenuate physiological and pathological elevations of spontaneous calcium release events.