Correlative studies support lipid peroxidation is linked to PrPres propagation as an early primary pathogenic event in prion disease

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Brazier, Marcus W, Lewis, Victoria A, Ciccotosto, Giuseppe D, Klug, Genevieve M, Lawson, Victoria A ORCID: 0000-0002-7362-7176, Cappai, Roberto ORCID: 0000-0002-9505-8496, Ironside, James W, Masters, Colin L ORCID: 0000-0003-3072-7940, Hill, Andrew F ORCID: 0000-0001-5581-2354, White, Anthony R ORCID: 0000-0003-1802-9891 and Collins, Steven J (2005) Correlative studies support lipid peroxidation is linked to PrPres propagation as an early primary pathogenic event in prion disease. Brain Research Bulletin, 68 (5). pp. 346-354. ISSN 0361-9230


To assess whether heightened oxidative stress plays an early and primary pathogenic role in transmissible spongiform encephalopathies (TSE), we undertook detailed correlative studies using a mouse-adapted model of human disease. The spatio-temporal evolution of the abnormal, protease-resistant isoform of the prion protein (PrPres) and neuropathological changes were correlated with the occurrence and type of oxidative stress. Heightened oxidative stress was demonstrated, but restricted to elevated levels of free aldehydic breakdown products of lipid peroxidation, affecting all brain regions to varying extents. The increase in lipid peroxidation was highest over the mid-incubation period, with the onset showing close temporal and general topographical concordance with the first detection of PrPres with both pre-empting the typical neuropathological changes of spongiform change, gliosis and neuronal loss. Further, prion propagation over the disease course was assessed using murine bioassay. This revealed that the initial rapid increase in infectivity titres was contemporaneous with the abrupt onset and maximisation of lipid peroxidation. The present results are an important extension to previous studies, showing that heightened oxidative stress in the form of lipid peroxidation is likely to constitute an early primary pathogenic event in TSE, associated temporally with the integral disease processes of prion propagation and PrPres formation, and consistent with causal links between these events and subsequent typical neuropathological changes.

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Item type Article
DOI 10.1016/j.brainresbull.2005.09.010
Official URL
Subjects Current > FOR (2020) Classification > 3101 Biochemistry and cell biology
Current > FOR (2020) Classification > 3207 Medical microbiology
Current > Division/Research > Chancellery
Keywords stress, oxidative stress, transmissible spongiform encephalopathies, TSE, prion protein
Citations in Scopus 66 - View on Scopus
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