Source:http://linkedlifedata.com/resource/pubmed/id/10841922
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1-2
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pubmed:dateCreated |
2000-8-11
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pubmed:abstractText |
Enhanced oxidant stress involved in the pathogenesis of cardiovascular (heart failure, atherosclerosis, ischemia-reperfusion injury), neurodegenerative (M. Alzheimer), metabolic (hypercholesterolemia, diabetes) and inflammatory disorders is mimicked by non-intermittent therapy with nitrovasodilators. We used this latter therapy model to study urinary 3-nitrotyrosine (n-tyr) excretion as a potential biomarker that may reflect the enhanced generation of reactive oxygen species. Namely, free or protein-bound n-tyr is formed in the organism by nitration of tyrosine (residues) via peroxynitrite (reaction product of NO&z.ccirf; and O(2)(-)&z. ccirf;). Free n-tyr content was analyzed by gas chromatography in urine obtained from healthy human subjects under a nitrite-limited diet during a two-day non-intermittent transdermal administration of glyceroltrinitrate (GTN; 0.4 mg/h) with or without vitamin C (Vit-C; 55 microg/kg/min) as antioxidant. Concomitant with the development of complete vascular tolerance (loss of dilator action), a progressive increase in urinary n-tyr excretion (up to 186+/-9 microg/day) was demonstrated in volunteers given GTN only. In contrast, when Vit-C was added, the GTN-induced increases in urinary n-tyr content were significantly suppressed (up to 130.20+/-6.91 microg/day), whereas Vit-C alone even decreased urinary n-tyr content (down to 34.00+/-5.66 microg/day), which was below control values (56.0+/-3.4 microg/day). Thus, urinary n-tyr may serve as a biomarker to detect changes in oxidant stress and thereby to evaluate the efficacy of therapeutic interventions aimed at reducing oxidant stress under various pathophysiological conditions.
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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/3-nitrotyrosine,
http://linkedlifedata.com/resource/pubmed/chemical/Ascorbic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers,
http://linkedlifedata.com/resource/pubmed/chemical/Nitroglycerin,
http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0009-8981
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
297
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
207-16
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10841922-Adult,
pubmed-meshheading:10841922-Ascorbic Acid,
pubmed-meshheading:10841922-Biological Markers,
pubmed-meshheading:10841922-Chromatography, Gas,
pubmed-meshheading:10841922-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:10841922-Female,
pubmed-meshheading:10841922-Humans,
pubmed-meshheading:10841922-Male,
pubmed-meshheading:10841922-Middle Aged,
pubmed-meshheading:10841922-Nitroglycerin,
pubmed-meshheading:10841922-Oxidative Stress,
pubmed-meshheading:10841922-Reference Values,
pubmed-meshheading:10841922-Tyrosine,
pubmed-meshheading:10841922-Urinalysis
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pubmed:year |
2000
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pubmed:articleTitle |
How urine analysis reflects oxidative stress--nitrotyrosine as a potential marker.
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pubmed:affiliation |
Institute of Applied Physiology, Albert-Ludwigs-University, Hermann-Herder-Strasse 7, D-79104, Freiburg, Germany. angphys@ruf.uni-freilburg.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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