Document Detail


Effect of acute increase of interstitial myocardial fluid on ventricular function in isolated working rat hearts.
MedLine Citation:
PMID:  9865455     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
An acute increase of myocardial interstitial fluid may affect ventricular function. In the present study we evaluated the effects of acute changes of myocardial tissue fluid on cardiac function and ultrastructural morphometry. Isolated rat hearts were perfused for 100 min in the working heart mode. Hearts were distributed into 5 groups: controls [perfused with Krebs-Henseleit (KH) isotonic buffer to rat plasma, KH, 287 mOsm], moderate hyposmotic perfusion (75% Hyposm: perfusion with 75% diluted KH, 216 mOsm), highly hyposmotic perfusion (60% Hyposm: perfusion with 60% diluted KH, 170 mOsm), afterload increase (Pre-over: isotonic perfused hearts subjected to an increase of afterload from 72 to 145 cm H2O) and ion dilution (Ion-dil: hearts perfused with a 60% KH with 115 mM sucrose, isotonic, 287 mOsm). We evaluated functional changes, markers of cellular necrosis or damage (CPK, LDH and purine release in coronary effluent), heart weight changes (weight gain and ww/dw ratio) and ultrastructural morphometry (analysis of cell damage, interstitial area, and mitochondrial alterations by a computerized image analysis system). The ww/dw ratio increased significantly only in 60% Hyposm (+140%, p < 0.001) and Pre-over (+63%, p < 0.001 vs control) groups. An impaired myocardial function in 60% Hyposm, Pre-over and Ion-dil groups was observed with cardiac failure at 50, 60 and 60 min, respectively. Enzyme release was significant higher in 60% Hyposm and Pre-over groups and was related to heart weight gain (r = 0.85, p < 0.001). Ultrastructural analysis confirmed a significant increase of interstitial space area (ISA) and mitochondrial damage in 60% Hyposm and Pre-over groups (p < 0.001); a significant (p < 0.05) increase was observed in the Ion-dil group; in 75% Hyposm group, a significant increase of mitochondrial damage was detected (p < 0.05). In brief, a higher functional and morphological deterioration was observed in hearts in which a more evident interstitial edema was detected (60% Hyposm and Pre-over groups). We conclude that, in the experimental condition, an acute increase of myocardial interstitial tissue fluid directly compromises left ventricular function and contributes to the ultrastructural damage to the myocardium.
Authors:
A Barsotti; P Di Napoli; F L Dini; M Soccio; P Di Iorio; S Gallina; M Di Muzio; A Modesti
Related Documents :
16785725 - Efficacy of cardiac mri in the evaluation of ischemic heart disease.
7012045 - Computerized quantitation of regional myocardial perfusion in man.
11015335 - Therapeutic angiogenesis with recombinant fibroblast growth factor-2 improves stress an...
15968605 - Myocardial perfusion in women with systemic lupus erythomatosus and no symptoms of coro...
23890685 - Pitfalls in diagnosing st elevation among patients with acute myocardial infarction.
18080705 - Current status of the surgical treatment of atrial fibrillation.
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of medicine     Volume:  29     ISSN:  0025-7850     ISO Abbreviation:  J Med     Publication Date:  1998  
Date Detail:
Created Date:  1999-03-12     Completed Date:  1999-03-12     Revised Date:  2003-11-14    
Medline Journal Info:
Nlm Unique ID:  7505566     Medline TA:  J Med     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  137-58     Citation Subset:  IM    
Affiliation:
Department of Cardiology and Cardiac Surgery, University of Chieti, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Blood Pressure / physiology
Enzymes / metabolism
Extracellular Space / physiology*
Heart / physiology*
Myocardial Contraction / physiology
Myocardium / metabolism
Purines / metabolism
Rats
Rats, Wistar
Ventricular Function, Left / physiology*
Chemical
Reg. No./Substance:
0/Enzymes; 0/Purines

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


Previous Document:  Decreased fecal bile acid output in patients with coronary atherosclerosis.
Next Document:  CD4+ and CD8+ lymphocyte and cortisol response patterns in elderly and young males after methylpredn...