Source:http://linkedlifedata.com/resource/pubmed/id/14654375
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2003-12-5
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pubmed:abstractText |
In the present study, we examined the effect of interleukin-2 (IL-2) on cardiomyocyte Ca(2+) handling. The effects of steady-state and transient changes in stimulation frequency on the intracellular Ca(2+) transient were investigated in isolated ventricular myocytes by spectrofluorometry. In the steady state (0.2 Hz) IL-2 (200 U/ml) decreased the amplitude of Ca(2+) transients induced by electrical stimulation and caffeine. At 1.25 mM extracellular Ca(2+) concentration ([Ca(2+)](o)), when the stimulation frequency increased from 0.2 to 1.0 Hz, diastolic Ca(2+) level and peak intracellular Ca(2+) concentration ([Ca(2+)](i)), as well as the amplitude of the transient, increased. The positive frequency relationships of the peak and amplitude of [Ca(2+)](i) transients were blunted in the IL-2-treated myocytes. The effect of IL-2 on the electrically induced [Ca(2+)](i) transient was not normalized by increasing [Ca(2+)](o) to 2.5 mM. IL-2 inhibited the frequency relationship of caffeine-induced Ca(2+) release. Blockade of sarcoplasmic reticulum (SR) Ca(2+)-ATPase with thapsigargin resulted in a significant reduction of the amplitude-frequency relationship of the transient similar to that induced by IL-2. The restitutions were not different between control and IL-2 groups at 1.25 mM [Ca(2+)](o), which was slowed in IL-2-treated myocytes when [Ca(2+)](o) was increased to 2.5 mM. There was no difference in the recirculation fraction (RF) between control and IL-2-treated myocytes at both 1.25 and 2.5 mM [Ca(2+)](o). The effects of IL-2 on frequency relationship, restitution, and RF may be due to depressed SR functions and an increased Na(+)-Ca(2+) exchange activity, but not to any change in L-type Ca(2+) channels.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphatases,
http://linkedlifedata.com/resource/pubmed/chemical/Caffeine,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Thapsigargin
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0022-2828
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
35
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1491-503
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14654375-Adenosine Triphosphatases,
pubmed-meshheading:14654375-Animals,
pubmed-meshheading:14654375-Caffeine,
pubmed-meshheading:14654375-Calcium,
pubmed-meshheading:14654375-Electric Stimulation,
pubmed-meshheading:14654375-Enzyme Inhibitors,
pubmed-meshheading:14654375-Heart Ventricles,
pubmed-meshheading:14654375-Interleukin-2,
pubmed-meshheading:14654375-Male,
pubmed-meshheading:14654375-Myocardium,
pubmed-meshheading:14654375-Myocytes, Cardiac,
pubmed-meshheading:14654375-Rats,
pubmed-meshheading:14654375-Rats, Sprague-Dawley,
pubmed-meshheading:14654375-Sarcoplasmic Reticulum,
pubmed-meshheading:14654375-Spectrometry, Fluorescence,
pubmed-meshheading:14654375-Thapsigargin
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pubmed:year |
2003
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pubmed:articleTitle |
Influence of interleukin-2 on Ca2+ handling in rat ventricular myocytes.
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pubmed:affiliation |
Department of Physiology, Zhejiang University School of Medicine, 353 Yan'an Road, Hangzhou 310031, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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