Source:http://linkedlifedata.com/resource/pubmed/id/16151967
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2005-12-29
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pubmed:abstractText |
In this study we tested the hypothesis that vasostatins could act as myocardial modulators in the mammalian heart. Using the Langendorff-perfused rat heart, the cardiac effects of the two recombinant human CGA N-terminal fragments STA-CGA1-78 and STA-CGA1-115, containing the vasostatin-1 (CGA 1-76) and vasostatin-2 (CGA 1-113) sequences, respectively, were evaluated at concentrations of 11 / 165 nM. Cardiac performance was evaluated by analyzing left ventricular pressure (LVP) and the rate pressure product (RPP: HR x LVP), used as indexes of contractile activity and cardiac work, respectively. Under basal conditions, STA-CGA1-78 at all concentrations tested elicited a dose-dependent negative inotropism (LVP variations ranging from -9.6% +/- 2 to -23% +/- 2.9) without affecting coronary pressure (CP). In contrast, STA-CGA1-115 increased CP at 110 and 165 nM without affecting inotropism. Both STA-CGA1-78 and STA-CGA1-115 counteracted the cardio-stimulatory effects of isoproterenol (ISO). The ISO-dependent positive chronotropism was unaffected by STA-CGA1-78, while being reduced by STA-CGA1-115. Both peptides abolished the ISO-induced positive inotropism without modifying either the beta-adrenergic-dependent coronary dilation or the ouabain-induced positive inotropism. The analysis of the percentage of variations of RPP in terms of EC50 values of ISO alone (-8.5 +/- 0.3; r2 = 0.88) and in presence of STA-CGA1-78 (11, or 33, or 65 nM: -7.7 +/- 0.15, r2 = 0.97; -7.7 +/- 0.15, r2 = 0.97; -7.8 +/- 0.78, r2 = 0.55, respectively) revealed a non-competitive type of antagonism of STA-CGA1-78. Taken together, these data suggest vasostatins as novel cardioregulatory peptides in mammals.
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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/Adrenergic beta-Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Cardiovascular Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Chromogranin A,
http://linkedlifedata.com/resource/pubmed/chemical/Chromogranins,
http://linkedlifedata.com/resource/pubmed/chemical/Isoproterenol,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/vasostatin I,
http://linkedlifedata.com/resource/pubmed/chemical/vasostatin II
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0300-8428
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
101
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
43-52
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16151967-Adrenergic beta-Agonists,
pubmed-meshheading:16151967-Amino Acid Sequence,
pubmed-meshheading:16151967-Animals,
pubmed-meshheading:16151967-Cardiovascular Agents,
pubmed-meshheading:16151967-Chromogranin A,
pubmed-meshheading:16151967-Chromogranins,
pubmed-meshheading:16151967-Heart,
pubmed-meshheading:16151967-Heart Rate,
pubmed-meshheading:16151967-Homeostasis,
pubmed-meshheading:16151967-Isoproterenol,
pubmed-meshheading:16151967-Male,
pubmed-meshheading:16151967-Molecular Sequence Data,
pubmed-meshheading:16151967-Myocardial Contraction,
pubmed-meshheading:16151967-Peptide Fragments,
pubmed-meshheading:16151967-Rats,
pubmed-meshheading:16151967-Rats, Wistar,
pubmed-meshheading:16151967-Recombinant Proteins,
pubmed-meshheading:16151967-Sequence Alignment
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pubmed:year |
2006
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pubmed:articleTitle |
Recombinant N-terminal fragments of chromogranin-A modulate cardiac function of the Langendorff-perfused rat heart.
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pubmed:affiliation |
Department of Pharmaco-Biology, University of Calabria, 87030, Arcavacata di Rende (CS), Italy. cerramc@unical.it
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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