Source:http://linkedlifedata.com/resource/pubmed/id/12388315
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2002-11-12
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pubmed:abstractText |
We developed an in situ assay system to simultaneously monitor intracellular Ca(2+) concentration ([Ca(2+)](i), fura 2 as indicator) and nitric oxide (NO) levels [4,5-diaminofluorescein as probe] in the intact endothelium of small bovine coronary arteries by using a fluorescent microscopic imaging technique with high-speed wavelength switching. Bradykinin (BK; 1 microM) stimulated a rapid increase in [Ca(2+)](i) followed by an increase in NO production in the endothelial cells. The protein tyrosine phosphatase inhibitor phenylarsine oxide (PAO; 10 microM) induced a gradual, small increase in [Ca(2+)](i) and a slow increase in intracellular NO levels. Removal of extracellular Ca(2+) and depletion of Ca(2+) stores completely blocked BK-induced increase in NO production but had no effect on PAO-induced NO production. However, a further reduction of [Ca(2+)](i) by application of BAPTA-AM or EGTA with ionomycin abolished the PAO-induced NO increase. These results indicate that a simultaneous monitoring of [Ca(2+)](i) and intracellular NO production in the intact endothelium is a powerful tool to study Ca(2+)-dependent regulation of endothelial nitric oxide synthase, which provides the first direct evidence for a permissive role of Ca(2+) in tyrosine phosphorylation-induced NO production.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Arsenicals,
http://linkedlifedata.com/resource/pubmed/chemical/Bradykinin,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Chelating Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Fluorescent Dyes,
http://linkedlifedata.com/resource/pubmed/chemical/Ionophores,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatases,
http://linkedlifedata.com/resource/pubmed/chemical/oxophenylarsine
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0363-6135
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
283
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
H2725-32
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:12388315-Animals,
pubmed-meshheading:12388315-Arsenicals,
pubmed-meshheading:12388315-Bradykinin,
pubmed-meshheading:12388315-Calcium,
pubmed-meshheading:12388315-Cattle,
pubmed-meshheading:12388315-Chelating Agents,
pubmed-meshheading:12388315-Coronary Vessels,
pubmed-meshheading:12388315-Endothelium, Vascular,
pubmed-meshheading:12388315-Enzyme Inhibitors,
pubmed-meshheading:12388315-Fluorescent Dyes,
pubmed-meshheading:12388315-Intracellular Fluid,
pubmed-meshheading:12388315-Ionophores,
pubmed-meshheading:12388315-Microscopy, Fluorescence,
pubmed-meshheading:12388315-Nitric Oxide,
pubmed-meshheading:12388315-Protein Tyrosine Phosphatases
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pubmed:year |
2002
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pubmed:articleTitle |
Simultaneous in situ monitoring of intracellular Ca2+ and NO in endothelium of coronary arteries.
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pubmed:affiliation |
Department of Pharmacology, Medical College of Wisconsin, Milwaukee 53226, USA.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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