Acute myocardial beta-adrenergic receptor dysfunction after cardiopulmonary bypass in patients with cardiac valve disease. Duke Heart Center Perioperative Desensitization Group
- PMID: 9852914
Acute myocardial beta-adrenergic receptor dysfunction after cardiopulmonary bypass in patients with cardiac valve disease. Duke Heart Center Perioperative Desensitization Group
Abstract
Background: Patients with cardiac valve disease (CVD) frequently have congestive heart failure (CHF) and chronic myocardial beta-adrenergic receptor (beta AR) desensitization. Cardiac surgery requiring cardiopulmonary bypass (CPB) is associated with increased plasma catecholamine concentrations, which might worsen myocardial beta AR function. We therefore tested the hypothesis that acute beta AR dysfunction occurs during CPB in patients with CVD.
Methods and results: After informed consent, 50 patients were enrolled. Right atrial biopsy samples were obtained at initiation and conclusion of CPB to assess beta AR density and adenylyl cyclase (AC) activity. Plasma catecholamine concentrations increased 3-fold during CPB (P < 0.01). Although beta AR density remained constant, isoproterenol-stimulated AC activity decreased significantly (approximately 30%; P < 0.005). AC activity decreased 22% and 24% with direct G protein (NaF) or AC (manganese) activation, respectively. Patients with or without preoperative CHF exhibited similar degrees of acute myocardial beta AR dysfunction during CPB.
Conclusions: Acute myocardial beta AR dysfunction occurs during CPB in patients with severe CVD requiring surgical correction, with or without preexisting CHF. The primary underlying mechanism involves functional uncoupling of the beta AR signal transduction pathway at the level of the AC moiety. This information should facilitate development of agents designed to prevent acute myocardial beta AR dysfunction during CPB, potentially leading to improved outcome in this high-risk population.
Similar articles
-
Acute depression of myocardial beta-adrenergic receptor signaling during cardiopulmonary bypass: impairment of the adenylyl cyclase moiety. Duke Heart Center Perioperative Desensitization Group.Anesthesiology. 1998 Sep;89(3):602-11. doi: 10.1097/00000542-199809000-00008. Anesthesiology. 1998. PMID: 9743395
-
Improved beta-adrenergic receptor function after coronary artery bypass grafting in patients with congestive heart failure.Coron Artery Dis. 1995 Dec;6(12):957-63. Coron Artery Dis. 1995. PMID: 8723018
-
Changes in beta-adrenoceptors in heart failure due to myocardial infarction are attenuated by blockade of renin-angiotensin system.Mol Cell Biochem. 2004 Aug;263(1-2):11-20. Mol Cell Biochem. 2004. PMID: 15524163
-
Genetic manipulation of myocardial beta-adrenergic receptor activation and desensitization.J Mol Cell Cardiol. 2004 Jul;37(1):11-21. doi: 10.1016/j.yjmcc.2004.03.014. J Mol Cell Cardiol. 2004. PMID: 15242731 Review.
-
Distinct beta-adrenergic receptor subtype signaling in the heart and their pathophysiological relevance.Sheng Li Xue Bao. 2004 Feb 25;56(1):1-15. Sheng Li Xue Bao. 2004. PMID: 14985822 Review.
Cited by
-
Preischemic infusion of alpha-human atrial natriuretic peptide elicits myoprotective effects against ischemia reperfusion in isolated rat hearts.Mol Cell Biochem. 2003 Jun;248(1-2):171-7. doi: 10.1023/a:1024148621505. Mol Cell Biochem. 2003. PMID: 12870670
-
Myocardial Dysfunction and Shock after Cardiac Arrest.Biomed Res Int. 2015;2015:314796. doi: 10.1155/2015/314796. Epub 2015 Sep 2. Biomed Res Int. 2015. PMID: 26421284 Free PMC article. Review.
-
The Regulator of G Protein Signaling Homologous Domain of G Protein-Coupled Receptor Kinase 2 Mediates Short-Term Desensitization of β3-Adrenergic Receptor.Front Pharmacol. 2020 Feb 21;11:113. doi: 10.3389/fphar.2020.00113. eCollection 2020. Front Pharmacol. 2020. PMID: 32153413 Free PMC article.
-
Postoperative atrial fibrillation in patients undergoing coronary artery bypass grafting or cardiac valve surgery: intraoperative use of landiolol.J Cardiothorac Surg. 2013 Jan 24;8:19. doi: 10.1186/1749-8090-8-19. J Cardiothorac Surg. 2013. PMID: 23347432 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Other Literature Sources
Medical
Research Materials