Document Detail


Role of polymorphonuclear leukocytes in reperfusion injury of globally ischemic rat heart.
MedLine Citation:
PMID:  7866939     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: Polymorphonuclear leukocytes (PMNs) have recently been observed to generate oxygen free radical (OFR) species during regional myocardial ischemia-reperfusion. This study evaluated the role of PMN-derived OFR in reperfusion injury of globally ischemic rat heart. METHODS: Isolated rat hearts were perfused with recirculating medium as follows: hydrogen peroxide; PMNs; PMNs plus phorbol myristate acetate (PMA); PMNs plus PMA plus OFR scavengers (superoxide dismutase [SOD] plus catalase, preprotection and reperfusion); ischemia-reperfusion (34 degrees C); ischemia-reperfusion (34 degrees C) plus OFR scavengers; ischemia-reperfusion (34 degrees C) plus PMNs; and ischemia-reperfusion (34 degrees C) plus PMNs plus OFR scavengers. Left ventricular (LV) systolic (developed pressure [Pmax], +dP/dt) and diastolic (left ventricular end-diastolic pressure [LVEDP], -dP/dt, LV compliance, LV wall stiffness) functions were evaluated. LV contracture development was studied by applying the quick stretch test. RESULTS: In vitro hydrogen peroxide perfusion significantly reduced LV contractility and caused a marked increase in LVEDP. PMN-derived OFR (mainly hydrogen peroxide) caused serious derangements in LV systolic and diastolic functions and produced a significant calcium-dependent LV contracture. Ischemia-reperfusion (34 degrees C) in the absence of PMNs produced predictable abnormalities in LV function and caused severe ATP-dependent LV contracture. Ischemia-reperfusion (34 degrees C) in the presence of PMNs significantly enhanced reperfusion injury. LVEDP increased considerably and a condition of irreversible contracture (stone heart) developed. OFR scavengers (SOD and catalase) were effective in preserving LV diastolic function and in neutralizing the additional component of injury caused by in vitro or in situ activation of PMNs. However, OFR scavengers failed to offer any significant improvement in LV systolic functions. CONCLUSIONS: Results of these studies indicate that: first, activated PMNs produce significant amounts of hydrogen peroxide; second, OFR released by activated PMNs during perfusion caused a significant depression of LV systolic and diastolic function; third, PMNs enhanced reperfusion injury of the globally ischemic rat heart; and fourth, the OFR scavengers SOD and catalase minimized changes in LV diastolic function, whereas LV systolic function showed little improvement.
Authors:
S A Malatiali; J S Juggi
Related Documents :
10218619 - Protective effects of ischemic preconditioning on lung ischemia reperfusion injury: an ...
3694209 - The effect of increased blood pressure on hemispheric lactate and water content during ...
10471349 - Trace amounts of albumin protect against ischemia and reperfusion injury in isolated ra...
9196859 - Effect of sodium-hydrogen exchange inhibition on functional and metabolic impairment pr...
2476119 - Pge1 and iloprost affect the high energy phosphates in the global ischemic and reperfus...
2470359 - Significance of the cardioprotective effect of prostanoids and indomethacin.
9582549 - Alcohol abuse: potential role in electrolyte disturbances and kidney diseases.
2531119 - Relative contributions of dietary na+ and cl- to salt-sensitive hypertension.
3024889 - Pressor sensitivity to angiotensin i and angiotensin ii during the development of exper...
Publication Detail:
Type:  In Vitro; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Canadian journal of cardiology     Volume:  11     ISSN:  0828-282X     ISO Abbreviation:  Can J Cardiol     Publication Date:  1995 Feb 
Date Detail:
Created Date:  1995-03-30     Completed Date:  1995-03-30     Revised Date:  2008-04-09    
Medline Journal Info:
Nlm Unique ID:  8510280     Medline TA:  Can J Cardiol     Country:  CANADA    
Other Details:
Languages:  eng     Pagination:  147-58     Citation Subset:  IM    
Affiliation:
Department of Physiology, Faculty of Medicine, Kuwait University.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Catalase / pharmacology
Free Radical Scavengers / pharmacology
Hydrogen Peroxide / metabolism,  pharmacology
Male
Myocardial Contraction / drug effects
Myocardial Reperfusion Injury / immunology*
Neutrophils / metabolism*
Perfusion
Rats
Reactive Oxygen Species / metabolism
Superoxide Dismutase / pharmacology
Superoxides / metabolism
Ventricular Function, Left / drug effects
Ventricular Pressure / drug effects
Chemical
Reg. No./Substance:
0/Free Radical Scavengers; 0/Reactive Oxygen Species; 11062-77-4/Superoxides; 7722-84-1/Hydrogen Peroxide; EC 1.11.1.6/Catalase; EC 1.15.1.1/Superoxide Dismutase

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


Previous Document:  Hypoxia preconditions rabbit myocardium by an adenosine receptor-mediated mechanism.
Next Document:  Bacterial and fungal flora in healthy eyes of birds of prey.