Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1995-7-6
pubmed:abstractText
Nitric oxide reacts with superoxide at a diffusion controlled rate to form peroxynitrite. Some studies have indicated that peroxynitrite underwent homolytic cleavage to give the highly toxic hydroxyl radical, while others have suggested that the decomposition of peroxynitrite did not generate hydroxyl radical. Because of this controversy, the fate of peroxynitrite decomposition was investigated using electron spin resonance (EPR) spectroscopy in combination with spin trapping technique. Utilizing 4-pyridyl 1-oxide N-tert-butylnitrone (4-POBN)/ethanol as a spin trapping system, we found that peroxynitrite, at physiological pH in either the absence or the presence of chelated iron, will produce hydroxyl radical. Further quantification experiments indicated that the yield of hydroxyl radical formation was only about 1-4%. Since the concentration of hydroxyl radical produced is so low, the cytotoxicity mediated by peroxynitrite might not be due to the formation of this free radical.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0006-3002
pubmed:author
pubmed:issnType
Print
pubmed:day
11
pubmed:volume
1244
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
62-8
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed:year
1995
pubmed:articleTitle
Does peroxynitrite generate hydroxyl radical?
pubmed:affiliation
Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore 21201, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't