Source:http://linkedlifedata.com/resource/pubmed/id/10747003
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2000-4-19
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pubmed:databankReference | |
pubmed:abstractText |
The goal of this study was to determine whether hypoxia alters expression of endothelial nitric oxide synthase (eNOS) in the systemic circulation. Rats breathed either air or 10% oxygen for 12 hours, 48 hours, or 7 days. Thoracic aortas were excised and either mounted in organ bath myographs or frozen in liquid nitrogen for later extraction of protein and RNA. eNOS protein (Western blotting) was decreased (20% of normoxic control) after 12 hours, 48 hours, and 7 days of hypoxia. eNOS mRNA (ribonuclease protection assay) was similarly reduced. Acetylcholine (10(-4) mol/L) reversed phenylephrine (10(-5) mol/L) preconstriction by 53.3+/-5.6% in aortic rings from normoxic rats and 26.1+/-4.8% in rings from rats exposed to hypoxia for 48 hours (P<0.05), with comparable impairment of relaxation by the calcium ionophore A23187 (10(-5) mol/L). Responses to diethylamine nitric oxide and 8-bromo-cGMP were unaffected. Aortic cGMP levels after incubation with acetylcholine (10(-6) mol/L) averaged 14.0+/-1.8 fmol/mg in rings from normoxic rats compared with 8.7+/-1.0 fmol/mg in rings from hypoxic rats (P<0. 05). Similarly, nitrate concentration (by capillary electrophoresis) in the media in which the rings were incubated was reduced in the hypoxic group (5.6+/-0.23 micromol/L for hypoxic rats and 7.8+/-0.7 micromol/L for normoxic rats). Impaired endothelial NO release may handicap the vascular responses that defend vital organ function during hypoxia.
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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/Cyclic GMP,
http://linkedlifedata.com/resource/pubmed/chemical/Nitrates,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type III,
http://linkedlifedata.com/resource/pubmed/chemical/Nos3 protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0009-7330
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
31
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pubmed:volume |
86
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
671-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10747003-Animals,
pubmed-meshheading:10747003-Anoxia,
pubmed-meshheading:10747003-Aorta,
pubmed-meshheading:10747003-Cyclic GMP,
pubmed-meshheading:10747003-Down-Regulation,
pubmed-meshheading:10747003-Endothelium, Vascular,
pubmed-meshheading:10747003-Male,
pubmed-meshheading:10747003-Molecular Sequence Data,
pubmed-meshheading:10747003-Nitrates,
pubmed-meshheading:10747003-Nitric Oxide Synthase,
pubmed-meshheading:10747003-Nitric Oxide Synthase Type III,
pubmed-meshheading:10747003-RNA, Messenger,
pubmed-meshheading:10747003-Rats,
pubmed-meshheading:10747003-Rats, Sprague-Dawley,
pubmed-meshheading:10747003-Time Factors,
pubmed-meshheading:10747003-Vasodilation
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pubmed:year |
2000
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pubmed:articleTitle |
Downregulation of endothelial nitric oxide synthase in rat aorta after prolonged hypoxia in vivo.
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pubmed:affiliation |
Meakins-Christie Laboratories, McGill University, Montréal, Québec, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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