Document Detail


Heart rate in the pathophysiology of coronary blood flow and myocardial ischaemia: benefit from selective bradycardic agents.
MedLine Citation:
PMID:  18223669     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Starting out from a brief description of the determinants of coronary blood flow (perfusion, pressure, extravascular compression, autoregulation, metabolic regulation, endothelium-mediated regulation and neurohumoral regulation) the present review highlights the overwhelming importance of metabolic regulation such that coronary blood flow is increased at increased heart rate under physiological circumstances and the overwhelming importance of extravascular compression such that coronary blood flow is decreased at increased heart rate through reduction of diastolic duration in the presence of severe coronary stenoses. The review goes on to characterize the role of heart rate in the redistribution of regional myocardial blood flow between a normal coronary vascular tree with preserved autoregulation and a poststenotic vasculature with exhausted coronary reserve. When flow is normalized by heart rate, there is a consistent close relationship of regional myocardial blood flow and contractile function for each single cardiac cycle no matter whether or not there is a coronary stenosis and what the actual blood flow is. beta-Blockade improves both flow and function along this relationship. When the heart rate reduction associated with beta-blockade is prevented by pacing, alpha-adrenergic coronary vasoconstriction is unmasked and both flow and function are deteriorated. Selective heart rate reduction, however, improves both flow and function without any residual negative effect such as unmasked alpha-adrenergic coronary vasoconstriction or negative inotropic action.
Authors:
G Heusch
Related Documents :
16760869 - How to discriminate between hibernating and stunned myocardium.
1383619 - Comparison of krn2391 with nicorandil and nifedipine on canine coronary blood flow: ant...
3775769 - Coronary dilator effect of mci-176, a new calcium channel blocker, in dogs.
431099 - Optimization of coronary perfusion rate during cardiac surgery in man.
3316109 - Immediate effects of graded ionic and nonionic contrast injections on coronary blood fl...
6723779 - Comparative response of the heart and coronary vasculature to catecholamines, aminophyl...
15272069 - Detection of aspergillus dna by a nested pcr assay is superior to blood culture in an e...
20201689 - Design of the silent cerebral infarct transfusion (sit) trial.
7487569 - The flow rate and electrolyte composition of whole saliva elicited by the use of sucros...
Publication Detail:
Type:  Journal Article; Review     Date:  2008-01-28
Journal Detail:
Title:  British journal of pharmacology     Volume:  153     ISSN:  0007-1188     ISO Abbreviation:  Br. J. Pharmacol.     Publication Date:  2008 Apr 
Date Detail:
Created Date:  2008-04-14     Completed Date:  2008-08-12     Revised Date:  2013-06-06    
Medline Journal Info:
Nlm Unique ID:  7502536     Medline TA:  Br J Pharmacol     Country:  England    
Other Details:
Languages:  eng     Pagination:  1589-601     Citation Subset:  IM    
Affiliation:
Institute for Pathophysiology, University of Essen Medical School, Essen, Germany. gerd.heusch@uk-essen.de
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adrenergic beta-Antagonists / pharmacology
Animals
Anti-Arrhythmia Agents / pharmacology
Benzazepines / pharmacology
Coronary Circulation / drug effects*
Heart Rate / drug effects*
Humans
Myocardial Ischemia / drug therapy*,  physiopathology
Chemical
Reg. No./Substance:
0/Adrenergic beta-Antagonists; 0/Anti-Arrhythmia Agents; 0/Benzazepines; 155974-00-8/ivabradine
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Comparative study on transduction and toxicity of protein transduction domains.
Next Document:  Agonist binding, agonist affinity and agonist efficacy at G protein-coupled receptors.