NR ARIG

AU Lekishvili,T.; Sassoon,J.; Thompsett,A.R.; Green,A.; Ironside,J.W.; Brown,D.R.

TI BSE and vCJD cause disturbance to uric acid levels

QU Experimental Neurology 2004 Nov; 190(1): 233-44

PT journal article

AB Bovine spongiform encephalopathy (BSE) and variant Creutzfeldt-Jakob disease (vCJD) are two new members of the family of neurodegenerative conditions termed prion diseases. Oxidative damage has been shown to occur in prion diseases and is potentially responsible for the rapid neurodegeneration that is central to the pathogenesis of these diseases. An important nonenzymatic antioxidant in the brain is uric acid. Analysis of uric acid in the brain and cerebrospinal fluid (CSF) of cases of BSE and CJD showed a specific reduction in CSF levels for both BSE and variant CJD, but not sporadic CJD. Further studies based on cell culture experiments suggested that uric acid in the brain was produced by microglia. Uric acid was also shown to inhibit neurotoxicity of a prion protein peptide, production of the abnormal prion protein isoform (PrPsc) by infected cells, and polymerization of recombinant prion protein. These findings suggest that changes in uric acid may aid differential diagnosis of vCJD. Uric acid could be used to inhibit cell death or PrPsc formation in prion disease.

MH Animals; Brain/*metabolism; Brain Chemistry; Cattle; Cell Survival/drug effects; Cells, Cultured; Creutzfeldt-Jakob Syndrome/cerebrospinal fluid/*metabolism; Dose-Response Relationship, Drug; Encephalopathy, Bovine Spongiform/cerebrospinal fluid/*metabolism; Humans; Microglia/metabolism/pathology/secretion; Neurons/drug effects/metabolism/pathology; Peptide Fragments/antagonists & inhibitors/pharmacology; PrPsc Proteins/biosynthesis; Prions/antagonists & inhibitors/pharmacology; Research Support, Non-U.S. Gov't; Uric Acid/analysis/*metabolism/pharmacology

AD Tamuna Lekishvili, Judyth Sassoon, Andrew R. Thompsett, David R. Brown, Department of Biology and Biochemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK; Alison Green, James W. Ironside, National CJD Surveillance Unit, Western General Hospital, Edinburgh, EH4 2XU, Scotland, UK

SP englisch

PO USA

EA pdf-Datei

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