Adenosine Receptor Reserve and Long-Term Potentiation: Unconventional Adaptive Mechanisms in Cardiovascular Diseases? - Aix-Marseille Université Access content directly
Journal Articles International Journal of Molecular Sciences Year : 2021

Adenosine Receptor Reserve and Long-Term Potentiation: Unconventional Adaptive Mechanisms in Cardiovascular Diseases?

Abstract

While the concept of a receptor reserve (spare receptors) is old, their presence on human cells as an adaptive mechanism in cardiovascular disease is a new suggestion. The presence of spare receptors is suspected when the activation of a weak fraction of receptors leads to maximal biological effects, in other words, when the half-maximal effective concentration (EC50) for a biological effect (cAMP production, for example) is lower than the affinity (KD) of the ligand for a receptor. Adenosine is an ATP derivative that strongly impacts the cardiovascular system via its four membrane receptors, named A1R, A2AR, A2BR, and A3R, with the A1R being more particularly involved in heart rhythm, while the A2AR controls vasodilation. After a general description of the tools necessary to explore the presence of spare receptors, this review focuses on the consequences of the presence of spare adenosine receptors in cardiovascular physiopathology. Finally, the role of the adenosinergic system in the long-term potentiation and its possible consequences on the physiopathology are also mentioned.
Fichier principal
Vignette du fichier
ijms-22-07584.pdf (11.46 Mo) Télécharger le fichier
Origin : Files produced by the author(s)

Dates and versions

hal-03653502 , version 1 (22-09-2023)

Identifiers

Cite

Régis Guieu, Michele Brignole, Jean Claude Deharo, Pierre Deharo, Giovanna Mottola, et al.. Adenosine Receptor Reserve and Long-Term Potentiation: Unconventional Adaptive Mechanisms in Cardiovascular Diseases?. International Journal of Molecular Sciences, 2021, 22 (14), pp.7584. ⟨10.3390/ijms22147584⟩. ⟨hal-03653502⟩
14 View
0 Download

Altmetric

Share

Gmail Facebook Twitter LinkedIn More