Source:http://linkedlifedata.com/resource/pubmed/id/19958762
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-3
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pubmed:dateCreated |
2010-1-27
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pubmed:abstractText |
The purpose of this study was to determine whether expression of inducible nitric oxide synthase (iNOS) is altered in vascular smooth muscle cells of type 2 diabetes rats. We used cultured aortic smooth muscle cells (ASMCs) isolated from male Goto-Kakizaki diabetes rats (G-K rats) aged 27-28weeks and age-matched Wistar rats (control rats). iNOS and extracellular signal-regulated kinase (ERK) were evaluated by immunoblot and/or immunochemical analyses, and NO production was evaluated by measuring NO(X) (NO(2) and NO(3)). Expression of iNOS was not detected in ASMCs of either G-K or control rats under a resting condition. Stimulation with interleukin-1beta (IL-1beta) induced iNOS expression, which was much greater in ASMCs from G-K rats than in ASMCs from control rats. When ASMCs were stimulated with IL-1beta, the number of iNOS-immunoreactive ASMCs from G-K rats increased more prominently than did the number of such ASMCs from control rats. IL-1beta-induced NO production was also much greater in ASMCs from G-K rats than in those from control rats. Both IL-1beta-induced iNOS expression and NO production in ASMCs of G-K and control rats were markedly reduced in the presence of an ERK inhibitor, U0126 or PD98059. Both basal and IL-1beta-stimulated levels of ERK activity were significantly higher in ASMCs from G-K rats than in ASMCs from control rats. The results suggest that iNOS induction is enhanced in cultured ASMCs from G-K rats and that this enhancement is associated with increased ERK activity.
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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/Blood Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Extracellular Signal-Regulated MAP...,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1beta,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type II
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1879-0712
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pubmed:author | |
pubmed:copyrightInfo |
Copyright (c) 2009 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
10
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pubmed:volume |
629
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1-6
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pubmed:meshHeading |
pubmed-meshheading:19958762-Animals,
pubmed-meshheading:19958762-Aorta,
pubmed-meshheading:19958762-Blood Glucose,
pubmed-meshheading:19958762-Body Weight,
pubmed-meshheading:19958762-Cells, Cultured,
pubmed-meshheading:19958762-Diabetes Mellitus,
pubmed-meshheading:19958762-Enzyme Induction,
pubmed-meshheading:19958762-Extracellular Signal-Regulated MAP Kinases,
pubmed-meshheading:19958762-Gene Expression Regulation, Enzymologic,
pubmed-meshheading:19958762-Interleukin-1beta,
pubmed-meshheading:19958762-Male,
pubmed-meshheading:19958762-Muscle, Smooth, Vascular,
pubmed-meshheading:19958762-Nitric Oxide,
pubmed-meshheading:19958762-Nitric Oxide Synthase Type II,
pubmed-meshheading:19958762-Rats
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pubmed:year |
2010
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pubmed:articleTitle |
Enhancement of interleukin-1beta-induced iNOS expression in cultured vascular smooth muscle cells of Goto-Kakizaki diabetes rats.
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pubmed:affiliation |
Department of Environmental and Preventive Medicine, Hyogo College of Medicine, Nishinomiya, Hyogo 663-8501, Japan. wakabaya@hyo-med.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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