http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2005030138-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b21d5a3bb51ba3469670cba79007d4a6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a6eb4b9da0c925fdf73685489d43c086
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6f7f90783864ce612aad24ba8eae406b
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-519
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K-
filingDate 2004-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3938bc1e337c1f294ecdf3ca5b331575
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe2b661101986c39a1cf7089d2c93667
publicationDate 2005-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2005030138-A2
titleOfInvention Methods of modulating inflammatory reactions by modulating xanthine oxidoreductase activity
abstract Evidence is presented that inflammation and injury involves activation of xanthine oxidoreductase (XOR) in the newly recruited mononuclear phagocytes (MNP). XOR has been shown to be increased predominantly in the MNP that increase rapidly in the lungs of rats that develop acute lung injury (ALI) following intratracheal cytokine insufflation. XOR was recovered from the MNP largely converted to its oxygen radical generating, reversible O-form, and alveolar MNP exhibited increased oxidative stress as evidenced by increased nitrotyrosine staining. Cytokine insufflation also increased alveolar cell apoptosis. A functional role for XOR in cytokine induced inflammation was demonstrated. Tungsten and allopurinol decreased MNP XOR induction, nitrotyrosine staining, inflammatory cell infiltration, and alveolar cell apoptosis. Transfer of control or allopurinol treated MNP into rat lungs, and confirmed a specific role for MNP XOR in promoting lung inflammation. These data indicate that XOR can contribute to lung inflammation by its expression and conversion in a highly mobile inflammatory cell population.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2165705-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012502962-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID105090953
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP79338
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP08505
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID65124
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ2MH06
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP09585
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID3077506
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ00511
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID100689317
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP78609
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID178381
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID958
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8MKH0
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226397149
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID3383
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ54LT2
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID117612159
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCH0YS58
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID100861193
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID177192
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO93337
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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID2213
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCD4A9I5
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393970

Total number of triples: 771.