Journal article

Ceruloplasmin dysfunction and therapeutic potential for Parkinson disease

S Ayton, P Lei, JA Duce, BXW Wong, A Sedjahtera, PA Adlard, AI Bush, DI Finkelstein

Annals of Neurology | WILEY-BLACKWELL | Published : 2013

Abstract

Ceruloplasmin is an iron-export ferroxidase that is abundant in plasma and also expressed in glia. We found a ∼80% loss of ceruloplasmin ferroxidase activity in the substantia nigra of idiopathic Parkinson disease (PD) cases, which could contribute to the pro-oxidant iron accumulation that characterizes the pathology. Consistent with a role for ceruloplasmin in PD etiopathogenesis, ceruloplasmin knockout mice developed parkinsonism that was rescued by iron chelation. Additionally, peripheral infusion of ceruloplasmin attenuated neurodegeneration and nigral iron elevation in the 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine mouse model for PD. These findings show, in principle, that intraveno..

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Grants

Funding Acknowledgements

Supported by funds from the Australian Research Council, Australian National Health and Medical Research Council, CRC for Mental Health, and Operational Infrastructure Support Victorian State Government. The Victorian Brain Bank Network is supported by the University of Melbourne, Mental Health Research Institute, Alfred Hospital, and Victorian Forensic Institute of Medicine, and funded by Neurosciences Australia and the National Health and Medical Research Council.