Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1994-8-11
pubmed:abstractText
Xanthine oxidase (XO) activity and hydroxyl radical (.OH) formation are widely proposed mediators of renal reperfusion injury, potentially altering the severity of, and recovery from, postischemic acute renal failure. The goal of this study was to ascertain whether combination XO inhibitor (oxypurinol) and .OH scavenger (Na benzoate) therapy, given at the time of renal ischemia, alters the extent of: (1) tubular necrosis and filtration failure; (2) DNA fragmentation/apoptosis (assessed in situ by terminal deoxynucleotidyl transferase reactivity); (3) early tubular regenerative responses (proliferating cell nuclear antigen expression; (3H)thymidine incorporation); and (4) the rate and/or degree of functional and morphologic repair. The effects of XO inhibition, .OH scavengers, and "catalytic" iron (FeSO4) on human proximal tubular cell proliferation in vitro were also assessed with a newly established cell line (HK-2). Male Sprague-Dawley rats were subjected to 35 min of bilateral renal arterial occlusion with or without oxypurinol/benzoate therapy. These agents did not alter the extent of tubular necrosis or filtration failure, proliferating cell nuclear antigen expression or thymidine incorporation, or the rate/extent of renal functional/morphologic repair. DNA fragmentation did not precede tubular necrosis, and it was unaffected by antioxidant therapy. By 5 days postischemia, both treatment groups demonstrated regenerating epithelial fronds that protruded into the lumina. These structures contained terminal deoxynucleotidyl transferase-reactive, but morphologically intact, cells, suggesting the presence of apoptosis. Oxypurinol and .OH scavengers (benzoate; dimethylthiourea) suppressed in vitro tubular cell proliferation; conversely, catalytic Fe had a growth-stimulatory effect. These results suggest that: (1) XO inhibition/.OH scavenger therapy has no discernible net effect on postischemic acute renal failure; (2) DNA fragmentation does not precede tubular necrosis, suggesting that it is not a primary mediator of ischemic cell death; and (3) antioxidants can be antiproliferative for human tubular cells, possibly mitigating their potential beneficial effects.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1046-6673
pubmed:author
pubmed:issnType
Print
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1588-97
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:7912960-Acute Kidney Injury, pubmed-meshheading:7912960-Animals, pubmed-meshheading:7912960-Antioxidants, pubmed-meshheading:7912960-Apoptosis, pubmed-meshheading:7912960-Benzoates, pubmed-meshheading:7912960-Benzoic Acid, pubmed-meshheading:7912960-Cell Division, pubmed-meshheading:7912960-Cells, Cultured, pubmed-meshheading:7912960-DNA Damage, pubmed-meshheading:7912960-DNA Nucleotidylexotransferase, pubmed-meshheading:7912960-Free Radical Scavengers, pubmed-meshheading:7912960-Humans, pubmed-meshheading:7912960-Ischemia, pubmed-meshheading:7912960-Kidney, pubmed-meshheading:7912960-Kidney Tubular Necrosis, Acute, pubmed-meshheading:7912960-Male, pubmed-meshheading:7912960-Nuclear Proteins, pubmed-meshheading:7912960-Oxypurinol, pubmed-meshheading:7912960-Proliferating Cell Nuclear Antigen, pubmed-meshheading:7912960-Rats, pubmed-meshheading:7912960-Rats, Sprague-Dawley, pubmed-meshheading:7912960-Regeneration, pubmed-meshheading:7912960-Reperfusion Injury, pubmed-meshheading:7912960-Xanthine Oxidase
pubmed:year
1994
pubmed:articleTitle
An evaluation of antioxidant effects on recovery from postischemic acute renal failure.
pubmed:affiliation
Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.