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Correlation between beta-adrenoceptors and G-protein-coupled receptor kinases in pretransplantation heart failure.

Authors :
Agüero J
Almenar L
D'Ocon P
Oliver E
Montó F
Moro J
Castelló A
Rueda J
Martínez-Dolz L
Sánchez-Lazaro I
Montero JA
Source :
Transplantation proceedings [Transplant Proc] 2008 Nov; Vol. 40 (9), pp. 3014-6.
Publication Year :
2008

Abstract

Introduction: Prolonged catecholamine overstimulation of the myocardium in chronic heart failure causes a reduction in the number and functionality of beta1-adrenoceptors (beta1-AR) of the heart. Desensitization of beta1-AR is mediated by their phosphorylation by a group of cytosolic kinases (G-protein-coupled receptor kinases GRK). In advanced heart failure, an increase in GRK levels associated with the severity of the disease has been observed.<br />Objective: The objective of this study was to analyze messenger RNA (mRNA) levels of beta1-AR in the myocardium of patients who underwent transplantation for advanced heart failure and their correlation with expression of the major cardiac isoenzymes of GRK.<br />Materials and Methods: Myocardial tissue samples were obtained from the left ventricles of 14 explanted hearts of patients who underwent transplantation for dilated (n = 7) and ischemic (n = 7) cardiomyopathy. RT-PCR techniques were used to analyze mRNA levels of beta1-AR and the isoenzymes GRK2, GRK3, and GRK5.<br />Results: We observed a significant correlation between beta1-AR and the 3 subtypes of GRK (R(2) = 0.668, 0.71, and 0.318, respectively).<br />Conclusions: In patients with advanced heart failure pretransplantation, we observed a significant correlation between beta1-AR and GRK2 and GRK3 levels. GRK5, the subtype predominantly expressed in the myocardium, showed a lesser correlation with beta1-AR levels.

Details

Language :
English
ISSN :
0041-1345
Volume :
40
Issue :
9
Database :
MEDLINE
Journal :
Transplantation proceedings
Publication Type :
Academic Journal
Accession number :
19010176
Full Text :
https://doi.org/10.1016/j.transproceed.2008.09.011