Literature DB >> 11082491

Increased ferric iron content and iron-induced oxidative stress in the brains of scrapie-infected mice.

N H Kim1, S J Park, J K Jin, M S Kwon, E K Choi, R I Carp, Y S Kim.   

Abstract

Scrapie is a transmissible neurodegenerative disease of sheep and goats. The neuropathological changes include vacuolation, astrocytosis, the development of amyloid plaques in some instances, and neuronal loss. The mechanisms involved in neuronal cell death in scrapie are not known. Recently, we reported the presence of oxidative stress in the brains of scrapie-infected animals and suggested that this is the main mechanism that induces neuronal cell loss. It is known that oxidative stress induced by free radicals is associated with iron accumulation; this association led to an examination of the levels of iron (total iron, Fe(2+) and Fe(3+)) in the brains of control and scrapie-infected mice by biochemical methods. In the scrapie-infected group, both the level of total iron and the Fe(3+) level were significantly increased in cerebral cortex, striatum, and brainstem as compared to the values in the control group. A shift in the ratio of Fe(2+)/Fe(3+) was observed in the same regions of infected mice. Additionally, in this scrapie model, we confirmed the presence of oxidative stress, as evidenced by the increase of free malondialdehyde. These results suggest that iron metabolism is changed and that iron-induced oxidative stress partly contributes to neurodegeneration in scrapie infection.

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Year:  2000        PMID: 11082491     DOI: 10.1016/s0006-8993(00)02907-3

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  20 in total

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2.  Alteration of iron regulatory proteins (IRP1 and IRP2) and ferritin in the brains of scrapie-infected mice.

Authors:  Boe-Hyun Kim; Yong-Chul Jun; Jae-Kwang Jin; Jae-Il Kim; Nam-Ho Kim; Elizabeth A Leibold; James R Connor; Eun-Kyoung Choi; Richard I Carp; Yong-Sun Kim
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Review 3.  Redox control of prion and disease pathogenesis.

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Review 4.  De novo mammalian prion synthesis.

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5.  Paradoxical role of prion protein aggregates in redox-iron induced toxicity.

Authors:  Dola Das; Xiu Luo; Ajay Singh; Yaping Gu; Soumya Ghosh; Chinmay K Mukhopadhyay; Shu G Chen; Man-Sun Sy; Qingzhong Kong; Neena Singh
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6.  Modulation of proteinase K-resistant prion protein in cells and infectious brain homogenate by redox iron: implications for prion replication and disease pathogenesis.

Authors:  Subhabrata Basu; Maradumane L Mohan; Xiu Luo; Bishwajit Kundu; Qingzhong Kong; Neena Singh
Journal:  Mol Biol Cell       Date:  2007-06-13       Impact factor: 4.138

Review 7.  Recent advances in prion chemotherapeutics.

Authors:  Valerie L Sim; Byron Caughey
Journal:  Infect Disord Drug Targets       Date:  2009-02

Review 8.  Iron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease.

Authors:  Neena Singh; Swati Haldar; Ajai K Tripathi; Matthew K McElwee; Katharine Horback; Amber Beserra
Journal:  Antioxid Redox Signal       Date:  2014-02-27       Impact factor: 8.401

Review 9.  Brain iron homeostasis: from molecular mechanisms to clinical significance and therapeutic opportunities.

Authors:  Neena Singh; Swati Haldar; Ajai K Tripathi; Katharine Horback; Joseph Wong; Deepak Sharma; Amber Beserra; Srinivas Suda; Charumathi Anbalagan; Som Dev; Chinmay K Mukhopadhyay; Ajay Singh
Journal:  Antioxid Redox Signal       Date:  2013-08-15       Impact factor: 8.401

Review 10.  Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson's, Huntington's, Alzheimer's, prions, bactericides, chemical toxicology and others as examples.

Authors:  Douglas B Kell
Journal:  Arch Toxicol       Date:  2010-08-17       Impact factor: 5.153

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