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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1976-2-2
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pubmed:abstractText |
Using both isotopic and spectrophotometric techniques to monitor the overall Ca++ binding and release reactions, we have studied the effects of the relative free concentrations of Ca++, sarcoplasmic reticulum fragments (SRF) protein, and ATP on spontaneous Ca++ release by SRF isolated from normal canine hearts. Low free [Ca++] was achieved by using a Ca-EGTA buffer; higher (micromolar) values were obtained by direct Ca++ additions throughout the reactions. ATP concentrations were stabilized by an ATP-regenerating system or an ATP trap. Concentrations of nucleotides in the reaction mixtures were also determined. Release depended in part on the [Ca++]/[ATP] and on the [ATP]. Spontaneous Ca++ release was prevented or slowed when the [ATP] was rapidly lowered with the ATP trap. ATP regeneration delayed, but did not prevent Ca++ release. Ca++-induced Ca++ release was found in the presence of ADP and ATP. Verapamil and D 600 did not affect release. The results may provide a basis for the slowed Ca++ release in SRF from failing hearts.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0363-5872
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
143-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1188150-Adenosine Diphosphate,
pubmed-meshheading:1188150-Adenosine Triphosphate,
pubmed-meshheading:1188150-Animals,
pubmed-meshheading:1188150-Binding Sites,
pubmed-meshheading:1188150-Calcium,
pubmed-meshheading:1188150-Cell-Free System,
pubmed-meshheading:1188150-Dogs,
pubmed-meshheading:1188150-Dose-Response Relationship, Drug,
pubmed-meshheading:1188150-Kinetics,
pubmed-meshheading:1188150-Myocardium,
pubmed-meshheading:1188150-Sarcoplasmic Reticulum
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pubmed:year |
1975
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pubmed:articleTitle |
Role of free calcium and ATP in calcium release from cardiac sarcoplasmic reticulum fragments.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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