Document Detail


Verapamil preserves myocardial contractility in the hereditary cardiomyopathy of the Syrian hamster.
MedLine Citation:
PMID:  6460569     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
We attempted to alter the inherited myocardial damage and loss of contractility of the cardiomyopathic Syrian hamster (strain U-MX7-1) by giving cardiac drugs that altered intracellular calcium and myocardial workload. Thirty-seven 21-day-old cardiomyopathic and thirty-seven 21-day-old normal hamsters were divided into five groups each: verapamil-, propranolol-, digoxin-, hydralazine-, and saline-injected. On their 90th day of life, the hamsters were killed. Of the five cardiomyopathic groups, only verapamil reduced myocardial damage. When both "control" and cardiomyopathic hamsters were treated with saline, digoxin, or propranolol, the cardiomyopathic hamsters had significantly less contractile force, maximal rate of force development, and maximum velocity of unloaded shortening. When both groups were treated with verapamil or hydralazine, there were no significant group differences in the indices of contractility. However, when saline-treated cardiomyopathic hamsters were compared with drug-treated cardiomyopathic hamsters, only verapamil preserved myocardial contractility. There was also a weak correlation between the Vmax and the actin-activated ATPase activity of the cardiomyopathic hamsters (r = 0.63, P less than 0.001). We conclude that verapamil helped protect the myocardium of genetically cardiomyopathic hamsters against structural damage, and helped preserve myocardial contractility.
Authors:
J L Rouleau; L H Chuck; G Hollosi; P Kidd; R E Sievers; J Wikman-Coffelt; W W Parmley
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Circulation research     Volume:  50     ISSN:  0009-7330     ISO Abbreviation:  Circ. Res.     Publication Date:  1982 Mar 
Date Detail:
Created Date:  1982-05-27     Completed Date:  1982-05-27     Revised Date:  2009-11-19    
Medline Journal Info:
Nlm Unique ID:  0047103     Medline TA:  Circ Res     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  405-12     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Actins / pharmacology
Adenosine Triphosphatases / metabolism
Animals
Cardiomyopathies / drug therapy,  genetics*,  pathology
Cricetinae
Digoxin / therapeutic use
Hydralazine / therapeutic use
Mesocricetus
Myocardial Contraction / drug effects*
Myocardium / pathology
Myosins / metabolism
Papillary Muscles / drug effects
Sodium Chloride / therapeutic use
Verapamil / therapeutic use*
Grant Support
ID/Acronym/Agency:
HL 23518/HL/NHLBI NIH HHS; HL 25847/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Actins; 20830-75-5/Digoxin; 52-53-9/Verapamil; 7647-14-5/Sodium Chloride; 86-54-4/Hydralazine; EC 3.6.1.-/Adenosine Triphosphatases; EC 3.6.4.1/Myosins

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


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