The alpha1-adrenergic receptors in cardiac hypertrophy: signaling mechanisms and functional implications
- PMID: 26169957
- DOI: 10.1016/j.cellsig.2015.06.009
The alpha1-adrenergic receptors in cardiac hypertrophy: signaling mechanisms and functional implications
Abstract
Cardiac hypertrophy is a complex remodeling process of the heart induced by physiological or pathological stimuli resulting in increased cardiomyocyte size and myocardial mass. Whereas cardiac hypertrophy can be an adaptive mechanism to stressful conditions of the heart, prolonged hypertrophy can lead to heart failure which represents the primary cause of human morbidity and mortality. Among G protein-coupled receptors, the α1-adrenergic receptors (α1-ARs) play an important role in the development of cardiac hypertrophy as demonstrated by numerous studies in the past decades, both in primary cardiomyocyte cultures and genetically modified mice. The results of these studies have provided evidence of a large variety of α1-AR-induced signaling events contributing to the defining molecular and cellular features of cardiac hypertrophy. Recently, novel signaling mechanisms have been identified and new hypotheses have emerged concerning the functional role of the α1-adrenergic receptors in the heart. This review will summarize the main signaling pathways activated by the α1-AR in the heart and their functional implications in cardiac hypertrophy.
Keywords: A-Kinase-Anchoring Protein-Lbc; Alpha1-adrenergic receptors; Cardiac hypertrophy; G protein coupled receptors; MAP kinases; Rho signaling.
Copyright © 2015 Elsevier Inc. All rights reserved.
Similar articles
-
The A-kinase anchoring protein (AKAP)-Lbc-signaling complex mediates alpha1 adrenergic receptor-induced cardiomyocyte hypertrophy.Proc Natl Acad Sci U S A. 2007 Jun 12;104(24):10140-5. doi: 10.1073/pnas.0701099104. Epub 2007 May 30. Proc Natl Acad Sci U S A. 2007. PMID: 17537920 Free PMC article.
-
Cardiac alpha1-adrenergic receptors: novel aspects of expression, signaling mechanisms, physiologic function, and clinical importance.Pharmacol Rev. 2013 Dec 24;66(1):308-33. doi: 10.1124/pr.112.007203. Print 2014. Pharmacol Rev. 2013. PMID: 24368739 Free PMC article. Review.
-
The alpha(1A/C)- and alpha(1B)-adrenergic receptors are required for physiological cardiac hypertrophy in the double-knockout mouse.J Clin Invest. 2003 Jun;111(11):1783-91. doi: 10.1172/JCI16100. J Clin Invest. 2003. PMID: 12782680 Free PMC article.
-
Multifarious molecular signaling cascades of cardiac hypertrophy: can the muddy waters be cleared?Pharmacol Res. 2010 Nov;62(5):365-83. doi: 10.1016/j.phrs.2010.07.003. Epub 2010 Jul 17. Pharmacol Res. 2010. PMID: 20643208 Review.
-
Cardiac 7-transmembrane-spanning domain receptor portfolios: diversify, diversify, diversify.J Clin Invest. 2006 Apr;116(4):875-7. doi: 10.1172/JCI28234. J Clin Invest. 2006. PMID: 16585959 Free PMC article.
Cited by
-
Relations of postural change in blood pressure with hypertension-mediated organ damage in middle-aged adults of the Framingham heart study: A cross-sectional study.Front Cardiovasc Med. 2022 Nov 1;9:1013876. doi: 10.3389/fcvm.2022.1013876. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 36386360 Free PMC article.
-
Contribution of DNA methylation in chronic stress-induced cardiac remodeling and arrhythmias in mice.FASEB J. 2019 Nov;33(11):12240-12252. doi: 10.1096/fj.201900100R. Epub 2019 Aug 30. FASEB J. 2019. PMID: 31431066 Free PMC article.
-
Suppressor of IKKɛ is an essential negative regulator of pathological cardiac hypertrophy.Nat Commun. 2016 Jun 1;7:11432. doi: 10.1038/ncomms11432. Nat Commun. 2016. PMID: 27249321 Free PMC article.
-
Quantifying Effects of Pharmacological Blockers of Cardiac Autonomous Control Using Variability Parameters.Front Physiol. 2017 Jan 23;8:10. doi: 10.3389/fphys.2017.00010. eCollection 2017. Front Physiol. 2017. PMID: 28167918 Free PMC article.
-
A novel cardiomyopathy phenotype linked to a CHD7 missense variant.Sci Rep. 2025 Jun 3;15(1):19429. doi: 10.1038/s41598-025-00606-1. Sci Rep. 2025. PMID: 40461563 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous