Scott Ayton1, Peng Lei1, James A. Duce1, Bruce X. Wong1, Amelia Sedjahtera1, Paul A. Adlard2,3, Ashley I. Bush2,1, David I. Finkelstein1,3
1Oxidation Biology Laboratory, Florey Institute for Neuroscience and Mental Health, Parkville, Victoria, Australia
2Department of Pathology, University of Melbourne, Parkville, Victoria, Australia
3Synaptic Neurobiology, Florey Institute for Neuroscience and Mental Health, Parkville, Victoria, Australia
Tóm tắt
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 intravenous ceruloplasmin may have therapeutic potential in PD. Ann Neurol 2013;73:554–559
