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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1993-3-3
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pubmed:abstractText |
The release of secretin was studied in secretin cell-enriched preparations isolated from canine duodenal mucosa. The crude enterocytes were isolated by treating the duodenal mucosa sequentially with collagenase and ethylenediaminetetraacetic acid. Secretin cell-enriched fraction was prepared by centrifugation of the crude enterocytes in a counterflow elutriation rotor to obtain a final preparation containing 3.2 +/- 0.3 pmol/10(6) cell of immunoreactive secretin, which was 13-fold greater than the crude cell preparation (N = 5). The cells were incubated in Hanks' balanced salt solution for 20 min at 37 degrees C under 95% O2/5% CO2 before adding various agents and further incubated for various periods of time. The amounts of secretin released into the medium and retained by the cells were then determined by a specific radioimmunoassay. The release of immunoreactive secretin was increased dose-dependently over the control by dibutyryl cyclic-3',5'-adenosine monophosphate, forskolin, 4 beta-12-O-tetradecanoylphorbol-13-acetate, the synthetic serine protease inhibitor, camostat, and the calcium ionophore, A23187. The effects of forskolin, the phorbol ester, and A23187 were time-dependent and not observed at 4 degrees C. The release of immunoreactive secretin was also stimulated by KCl in high concentration and by sodium oleate. The effect of A23187 was abolished in a Ca(2+)-free medium, while those of dibutyryl cyclic-3',5'-adenosine monophosphate and forskolin were potentiated by 3-isobutyl-1-methylxanthine, which did not have a significant effect when added alone. These results indicate that the release of secretin is regulated by both Ca(2+)- and cyclic-3',5'-adenosine monophosphate-dependent mechanisms.2+ release.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0163-2116
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
38
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
344-52
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8425447-Animals,
pubmed-meshheading:8425447-Cell Separation,
pubmed-meshheading:8425447-Cells, Cultured,
pubmed-meshheading:8425447-Chromatography, High Pressure Liquid,
pubmed-meshheading:8425447-Dogs,
pubmed-meshheading:8425447-Dose-Response Relationship, Drug,
pubmed-meshheading:8425447-Drug Synergism,
pubmed-meshheading:8425447-Duodenum,
pubmed-meshheading:8425447-Immunohistochemistry,
pubmed-meshheading:8425447-Intestinal Mucosa,
pubmed-meshheading:8425447-Secretin,
pubmed-meshheading:8425447-Stimulation, Chemical,
pubmed-meshheading:8425447-Time Factors
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pubmed:year |
1993
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pubmed:articleTitle |
Characterization of secretin release in secretin cell-enriched preparation isolated from canine duodenal mucosa.
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pubmed:affiliation |
University of Rochester School of Medicine and Dentistry, Department of Medicine, New York 14642.
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pubmed:publicationType |
Journal Article,
Comparative Study
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