pubmed-article:10694238 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10694238 | lifeskim:mentions | umls-concept:C1882561 | lld:lifeskim |
pubmed-article:10694238 | lifeskim:mentions | umls-concept:C0003075 | lld:lifeskim |
pubmed-article:10694238 | lifeskim:mentions | umls-concept:C0010654 | lld:lifeskim |
pubmed-article:10694238 | lifeskim:mentions | umls-concept:C0441472 | lld:lifeskim |
pubmed-article:10694238 | lifeskim:mentions | umls-concept:C1425284 | lld:lifeskim |
pubmed-article:10694238 | lifeskim:mentions | umls-concept:C2754938 | lld:lifeskim |
pubmed-article:10694238 | lifeskim:mentions | umls-concept:C0443199 | lld:lifeskim |
pubmed-article:10694238 | lifeskim:mentions | umls-concept:C0068882 | lld:lifeskim |
pubmed-article:10694238 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:10694238 | pubmed:dateCreated | 2000-4-24 | lld:pubmed |
pubmed-article:10694238 | pubmed:abstractText | 1. The effects of L-cysteine were tested in rat aortic rings on responses to nitric oxide free radical (NO(*)), nitroxyl (NO(-)) derived from Angeli's salt and endothelium-derived relaxing factor (EDRF) activated by acetylcholine, ATP and the calcium ionophore A23187. Concentrations of 300 microM or less of L-cysteine had no effect on responses. 2. Relaxations produced by exogenous NO(*) (0.25 - 2.5 microM) were markedly prolonged and relaxations produced by sodium nitroprusside (0.001 - 0.3 microM) were enhanced by 1 and 3 mM L-cysteine. The enhancements by L-cysteine of responses to NO(*) and sodium nitroprusside may be attributed to the formation of S-nitrosocysteine. 3. Relaxations mediated by the nitroxyl anion (0.3 microM) donated from Angeli's salt were more prolonged than those produced by NO(*), and nitroxyl-induced relaxations were reduced by L-cysteine (1 and 3 mM). 4. EDRF-mediated relaxations produced by acetylcholine (0.01 - 10 microM), ATP (3 - 100 microM) and the calcium ionophore A23187 (0.1 microM) were significantly reduced by 3 mM L-cysteine. 5. The similarity between the inhibitory effects of L-cystei on responses to EDRF and on those to nitroxyl suggests that a component of the response to EDRF may be mediated by nitroxyl anion. | lld:pubmed |
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pubmed-article:10694238 | pubmed:language | eng | lld:pubmed |
pubmed-article:10694238 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10694238 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:10694238 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10694238 | pubmed:month | Jan | lld:pubmed |
pubmed-article:10694238 | pubmed:issn | 0007-1188 | lld:pubmed |
pubmed-article:10694238 | pubmed:author | pubmed-author:RandM JMJ | lld:pubmed |
pubmed-article:10694238 | pubmed:author | pubmed-author:EllisAA | lld:pubmed |
pubmed-article:10694238 | pubmed:author | pubmed-author:KoC PCP | lld:pubmed |
pubmed-article:10694238 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10694238 | pubmed:volume | 129 | lld:pubmed |
pubmed-article:10694238 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10694238 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10694238 | pubmed:pagination | 315-22 | lld:pubmed |
pubmed-article:10694238 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:10694238 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:10694238 | pubmed:articleTitle | Differential actions of L-cysteine on responses to nitric oxide, nitroxyl anions and EDRF in the rat aorta. | lld:pubmed |
pubmed-article:10694238 | pubmed:affiliation | Pharmacology Research Unit, Department of Medical Laboratory Science, RMIT University, GPO Box 2476V, Melbourne, Victoria, 3001, Australia. | lld:pubmed |
pubmed-article:10694238 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10694238 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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