| pubmed-article:2434322 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2434322 | lifeskim:mentions | umls-concept:C0015859 | lld:lifeskim |
| pubmed-article:2434322 | lifeskim:mentions | umls-concept:C0439861 | lld:lifeskim |
| pubmed-article:2434322 | lifeskim:mentions | umls-concept:C0036536 | lld:lifeskim |
| pubmed-article:2434322 | lifeskim:mentions | umls-concept:C0036537 | lld:lifeskim |
| pubmed-article:2434322 | lifeskim:mentions | umls-concept:C0040578 | lld:lifeskim |
| pubmed-article:2434322 | lifeskim:mentions | umls-concept:C1373045 | lld:lifeskim |
| pubmed-article:2434322 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:2434322 | pubmed:dateCreated | 1987-4-6 | lld:pubmed |
| pubmed-article:2434322 | pubmed:abstractText | To study the roles of substance P (SP) and endogenous peptidases in regulating mucus secretion from ferret trachea, we measured the SP-induced release of 35SO4-labeled macromolecules after incubating segments of trachea in Ussing chambers in the presence and absence of selected inhibitors of proteolytic enzymes. Our strategy was based on the idea that if endogenous peptidases degrade SP, then inhibitors of these enzymes should potentiate SP-induced secretion. We found that tracheas of ferrets contained SP-like immunoreactivity, and that SP stimulated the release of bound 35SO4 with rapid onset and offset. Eighty-five percent of the total macromolecular radioactivity released was contained in fractions of molecular weights greater than 10(6). The response to SP was concentration-dependent and reproducible. Thiorphan potentiated the secretory response to SP in a concentration-dependent fashion and phosphoramidon potentiated SP-induced secretion, whereas other inhibitors of proteinases and peptidases were without effects. These results suggest that substance P may regulate mucus secretion in ferrets, and that enkephalinase (dipeptidyl carboxypeptidase II, EC 3.4.24.11) in the airway degrades SP in a physiologically significant fashion, and thereby regulates peptide-induced secretion. | lld:pubmed |
| pubmed-article:2434322 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2434322 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:2434322 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:2434322 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2434322 | pubmed:issn | 0190-2148 | lld:pubmed |
| pubmed-article:2434322 | pubmed:author | pubmed-author:NadelJ AJA | lld:pubmed |
| pubmed-article:2434322 | pubmed:author | pubmed-author:RamachandranJ... | lld:pubmed |
| pubmed-article:2434322 | pubmed:author | pubmed-author:GoldMM | lld:pubmed |
| pubmed-article:2434322 | pubmed:author | pubmed-author:CaugheyGG | lld:pubmed |
| pubmed-article:2434322 | pubmed:author | pubmed-author:CorralesRR | lld:pubmed |
| pubmed-article:2434322 | pubmed:author | pubmed-author:VarsanoSS | lld:pubmed |
| pubmed-article:2434322 | pubmed:author | pubmed-author:BorsonD BDB | lld:pubmed |
| pubmed-article:2434322 | pubmed:author | pubmed-author:ViroNN | lld:pubmed |
| pubmed-article:2434322 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2434322 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:2434322 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2434322 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2434322 | pubmed:pagination | 21-36 | lld:pubmed |
| pubmed-article:2434322 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:2434322 | pubmed:meshHeading | pubmed-meshheading:2434322-... | lld:pubmed |
| pubmed-article:2434322 | pubmed:year | 1987 | lld:pubmed |
| pubmed-article:2434322 | pubmed:articleTitle | Enkephalinase inhibitors potentiate substance P-induced secretion of 35SO4-macromolecules from ferret trachea. | lld:pubmed |
| pubmed-article:2434322 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2434322 | pubmed:publicationType | In Vitro | lld:pubmed |
| pubmed-article:2434322 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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