Source:http://linkedlifedata.com/resource/pubmed/id/14564523
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2003-12-3
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pubmed:abstractText |
The production of nitric oxide (NO) by constitutive nitric oxide synthase (NOS) was investigated in isolated rat pancreatic islets and dispersed beta-cells. Double-immunocytochemical analyses with a confocal microscope demonstrated the presence of NOS1 in alpha-, beta-, delta-, and PP-cells and that of NOS3 in beta-, delta-, and PP-cells, but not alpha-cells, in the isolated rat islets. Image analyses with the NO-reactive fluorescence dye DAF-2 clearly showed that an elevation in glucose concentrations from 0 to 11.1 mM increased intracellular NO in most cells of the isolated islets. The glucose-induced elevation of intracellular NO in the islet cells was abolished in the presence of the Ca2+ channel blocker nicardipine and after treatment with the NOS inhibitor NG-nitro-L-arginine. Similarly, the ATP-sensitive K+ channel blocker tolbutamide, which elevates intracellular Ca2+ concentrations, increased DAF-2 fluorescence in most cells of the isolated islets. In isolated beta-cells, 11.1 mM glucose increased DAF-2 fluorescence, which was suppressed by NG-nitro-L-arginine and by reducing the glucose concentration to 0 mM. DAF-2 fluorescence in beta-cells was also increased by 50 mM K+, which was suppressed by NG-nitro-L-arginine. These results suggest that NOS1 and NOS3 are present in rat pancreatic beta-cells, and that glucose produces NO by Ca(2+)-dependent activation of the constitutive NOS isoforms.
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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/Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type I,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type III,
http://linkedlifedata.com/resource/pubmed/chemical/Nos1 protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Nos3 protein, rat
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0031-6768
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
447
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
305-11
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14564523-Animals,
pubmed-meshheading:14564523-Glucose,
pubmed-meshheading:14564523-Immunohistochemistry,
pubmed-meshheading:14564523-Islets of Langerhans,
pubmed-meshheading:14564523-Male,
pubmed-meshheading:14564523-Nitric Oxide,
pubmed-meshheading:14564523-Nitric Oxide Synthase,
pubmed-meshheading:14564523-Nitric Oxide Synthase Type I,
pubmed-meshheading:14564523-Nitric Oxide Synthase Type III,
pubmed-meshheading:14564523-Rats,
pubmed-meshheading:14564523-Rats, Wistar
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pubmed:year |
2003
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pubmed:articleTitle |
Constitutive nitric oxide synthases in rat pancreatic islets: direct imaging of glucose-induced nitric oxide production in beta-cells.
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pubmed:affiliation |
Department of Cellular and Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Shizuoka City, 422-8526, Shizuoka, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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