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Diverse regulation of cardiac expression of relaxin receptor by α1- and β1-adrenoceptors.
- Source :
-
Cardiovascular drugs and therapy [Cardiovasc Drugs Ther] 2014 Jun; Vol. 28 (3), pp. 221-8. - Publication Year :
- 2014
-
Abstract
- Purpose: Relaxin, a new drug for heart failure therapy, exerts its cardiac actions through relaxin family peptide receptor 1 (RXFP1). Factors regulating RXFP1 expression remain unknown. We have investigated effects of activation of adrenoceptors (AR), an important modulator in the development and prognosis of heart failure, on expression of RXFP1 in rat cardiomyocytes and mouse left ventricles (LV).<br />Methods: Expression of RXFP1 at mRNA (real-time PCR) and protein levels (immunoblotting) was measured in cardiomyocytes treated with α- and β-AR agonists or antagonists. RXFP1 expression was also determined in the LV of transgenic mouse strains with cardiac-restricted overexpression of α1A-, α1B- or β2-AR. Specific inhibitors were used to explore signal pathways involved in α1-AR mediated regulation of RXFP1 in cardiomyocytes.<br />Results: In cultured cardiomyocytes, α1-AR stimulation resulted in 2-3 fold increase in RXFP1 mRNA (P < 0.001), which was blocked by specific inhibitors for protein kinase C (PKC) or mitogen-activated protein kinases/extracellular signal-regulated kinases (MAPK/ERK). Activation of β1-, but not β2-AR, significantly inhibited RXFP1 expression (P < 0.001). Relative to respective wild-type controls, RXFP1 mRNA levels in the LV of mice overexpressing α1A- or α1B-AR were increased by 3- or 10-fold, respectively, but unchanged in β2-AR transgenic hearts. Upregulation by α1-AR stimulation RXFP1 expression was confirmed at protein levels both in vitro and in vivo.<br />Conclusions: Expression of RXFP1 was up-regulated by α1-AR but suppressed by β-AR, mainly β1-AR subtype, in cardiomyocytes. Future studies are warranted to characterize the functional significance of such regulation, especially in the setting of heart failure.
- Subjects :
- Adrenergic alpha-Agonists pharmacology
Adrenergic alpha-Antagonists pharmacology
Adrenergic beta-Agonists pharmacology
Adrenergic beta-Antagonists pharmacology
Animals
Female
Heart Ventricles drug effects
Heart Ventricles metabolism
Male
Mice
Mice, Transgenic
Myocytes, Cardiac metabolism
RNA, Messenger metabolism
Rats
Rats, Sprague-Dawley
Real-Time Polymerase Chain Reaction
Receptors, Adrenergic, alpha-1 drug effects
Receptors, Adrenergic, beta-1 drug effects
Receptors, G-Protein-Coupled genetics
Receptors, Peptide genetics
Up-Regulation drug effects
Myocytes, Cardiac drug effects
Receptors, Adrenergic, alpha-1 metabolism
Receptors, Adrenergic, beta-1 metabolism
Receptors, G-Protein-Coupled drug effects
Receptors, Peptide drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1573-7241
- Volume :
- 28
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Cardiovascular drugs and therapy
- Publication Type :
- Academic Journal
- Accession number :
- 24852484
- Full Text :
- https://doi.org/10.1007/s10557-014-6525-x