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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1983-9-9
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pubmed:abstractText |
The aim of this study was to determine if a prostaglandin-related material--in particular prostacyclinlike substance--could explain our previous findings showing that a sublethal dose of endotoxin caused the early release of a serum lipid-soluble factor able to decrease various activities of cultured rat heart cells (CRHC) through an intracellular calcium dysregulation. Sera were sampled from rats 4 h after administration of 2 mg/kg E coli endotoxin (E) and their cardiodepressant effect on CRHC determined by an electrooptical technique. E-treated rat serum (ETRS) cardiodepressant effect was compared to that of 0.1 ng/ml prostacyclin (PGI2) and of 0.029 ng/ml nifedipine, a calcium antagonist. The reversal effect of caffeine, a substance known for its positive inotropic effect by increasing intracellular calcium availability at the sarcoplasmic reticulum site, has been tested against the depressant effect of ETRS, PGI2, and nifedipine. Results: 1) Compared to control, serum from endotoxin-treated rats with or without imidazole pretreatment depressed contractility of CRHC in a similar fashion, whereas pretreatment with indomethacin had a much less marked effect; 2) PGI2, nifedipine, and ETRS depressed CRHC contractility in much the same way; 3) caffeine reversed the depressant effect of PGI2 and ETRS, but was much less effective against nifedipine effect. These results suggest that the cardiodepressant effect of ETRS is mediated by a prostaglandinlike substance, other than thromboxane, acting through reduced intracellular calcium availability. PGI2 or PGI2-related material is consistent with such a depressant effect and such a mechanism.
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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/Caffeine,
http://linkedlifedata.com/resource/pubmed/chemical/Epoprostenol,
http://linkedlifedata.com/resource/pubmed/chemical/Imidazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Indomethacin,
http://linkedlifedata.com/resource/pubmed/chemical/Myocardial Depressant Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Nifedipine,
http://linkedlifedata.com/resource/pubmed/chemical/imidazole
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pubmed:status |
MEDLINE
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pubmed:issn |
0195-878X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
161-71
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6349296-Animals,
pubmed-meshheading:6349296-Caffeine,
pubmed-meshheading:6349296-Cells, Cultured,
pubmed-meshheading:6349296-Depression, Chemical,
pubmed-meshheading:6349296-Epoprostenol,
pubmed-meshheading:6349296-Imidazoles,
pubmed-meshheading:6349296-Indomethacin,
pubmed-meshheading:6349296-Male,
pubmed-meshheading:6349296-Myocardial Contraction,
pubmed-meshheading:6349296-Myocardial Depressant Factor,
pubmed-meshheading:6349296-Nifedipine,
pubmed-meshheading:6349296-Peptide Biosynthesis,
pubmed-meshheading:6349296-Rats,
pubmed-meshheading:6349296-Shock, Septic
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pubmed:year |
1983
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pubmed:articleTitle |
Indomethacin suppresses the early cardiodepressant factor released by endotoxin in the rat: possible involvement of a prostacyclin-related material.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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