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Adenine nucleotide metabolism by isolated kidney tubules during oxygen deprivation

dc.contributor.authorWeinberg, Joel M.en_US
dc.date.accessioned2006-04-07T20:18:15Z
dc.date.available2006-04-07T20:18:15Z
dc.date.issued1988-06en_US
dc.identifier.citationWeinberg, Joel M. (1988/06)."Adenine nucleotide metabolism by isolated kidney tubules during oxygen deprivation." Biochemical Medicine and Metabolic Biology 39(3): 319-329. <http://hdl.handle.net/2027.42/27280>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WBN-4C4NVS8-DB/2/8a0b9595e66b3bb2acf6030f5a5ddc8ben_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27280
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3395511&dopt=citationen_US
dc.description.abstractSuspensions enriched in isolated rabbit proximal tubules were subjected to varying degrees of oxygen deprivation-induced injury by incubating them under hypoxic conditions at pH 7.4 or pH 6.6 or under high density pelleted conditions and adenine nucleotide degradation was characterized. The major metabolite was hypoxanthine. Its levels increased with the extent of irreversible injury. It was not further degraded or salvaged. Recovery of cell ATP during reoxygenation was predominantly from the remaining cell nucleotides. Allopurinol did not alter the pattern of purine metabolism or the extent of cell injury. These observations provide information on the intrinsic purine metabolic capacity of renal tubule cells during oxygen deprivation which is relevant to understanding both the salvage mechanisms available in these cells as well as the contribution of purine metabolism to the pathogenesis of oxygen deprivation-induced tubule cell injury.en_US
dc.format.extent779163 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleAdenine nucleotide metabolism by isolated kidney tubules during oxygen deprivationen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Nephrology, Department of Internal Medicine, Veterans Administration Medical Center, and University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.identifier.pmid3395511en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/27280/1/0000296.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0885-4505(88)90092-8en_US
dc.identifier.sourceBiochemical Medicine and Metabolic Biologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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