Lhermitte, J., Kraus, W. M. & McAlpine, D. Original Papers: On the occurrence of abnormal deposits of iron in the brain in parkinsonism with special reference to its localisation. J. Neurol. Psychopathol. 5, 195–208 (1924).
Article CAS PubMed PubMed Central Google Scholar
Dexter, D. T. et al. Increased nigral iron content in postmortem parkinsonian brain. Lancet 2, 1219–1220 (1987).
Article CAS PubMed Google Scholar
Dexter, D. T. et al. Alterations in the levels of iron, ferritin and other trace metals in Parkinson’s disease and other neurodegenerative diseases affecting the basal ganglia. Brain 114, 1953–1975 (1991).
Dexter, D. T. et al. Increased nigral iron content and alterations in other metal ions occurring in brain in Parkinson’s disease. J. Neurochem 52, 1830–1836 (1989).
Article CAS PubMed Google Scholar
Mann, V. M. et al. Complex I, iron, and ferritin in Parkinson’s disease substantia nigra. Ann. Neurol. 36, 876–881 (1994).
Article CAS PubMed Google Scholar
Sofic, E. et al. Increased iron (III) and total iron content in post mortem substantia nigra of parkinsonian brain. J. Neural Transm. 74, 199–205 (1988).
Article CAS PubMed Google Scholar
Sofic, E. et al. Selective increase of iron in substantia nigra zona compacta of parkinsonian brains. J. Neurochem 56, 978–982 (1991).
Article CAS PubMed Google Scholar
Riederer, P. et al. Transition metals, ferritin, glutathione, and ascorbic acid in parkinsonian brains. J. Neurochem 52, 515–520 (1989).
Article CAS PubMed Google Scholar
Antonini, A. et al. T2 relaxation time in patients with Parkinson’s disease. Neurology 43, 697–700 (1993).
Article CAS PubMed Google Scholar
Castellani, R. J., Siedlak, S. L., Perry, G. & Smith, M. A. Sequestration of iron by Lewy bodies in Parkinson’s disease. Acta Neuropathol. 100, 111–114 (2000).
Article CAS PubMed Google Scholar
Chen, B. et al. Interactions between iron and alpha-synuclein pathology in Parkinson’s disease. Free Radic. Biol. Med. 141, 253–260 (2019).
Article CAS PubMed Google Scholar
Berg, D. et al. Iron accumulation in the substantia nigra in rats visualized by ultrasound. Ultrasound Med. Biol. 25, 901–904 (1999).
Article CAS PubMed Google Scholar
Berg, D. et al. Echogenicity of the substantia nigra: association with increased iron content and marker for susceptibility to nigrostriatal injury. Arch. Neurol. 59, 999–1005 (2002).
Kaur, D. et al. Genetic or pharmacological iron chelation prevents MPTP-induced neurotoxicity in vivo: a novel therapy for Parkinson’s disease. Neuron 37, 899–909 (2003).
Article CAS PubMed Google Scholar
Devos, D. et al. Targeting chelatable iron as a therapeutic modality in Parkinson’s disease. Antioxid. Redox Signal 21, 195–210 (2014).
Article CAS PubMed PubMed Central Google Scholar
Oakley, A. E. et al. Individual dopaminergic neurons show raised iron levels in Parkinson disease. Neurology 68, 1820–1825 (2007).
Article CAS PubMed Google Scholar
Iranzo, A. et al. Neurodegenerative disease status and post-mortem pathology in idiopathic rapid-eye-movement sleep behaviour disorder: an observational cohort study. Lancet Neurol. 12, 443–453 (2013).
Sun, J. et al. Quantitative evaluation of iron content in idiopathic rapid eye movement sleep behavior disorder. Mov. Disord. 35, 478–485 (2020).
Article CAS PubMed Google Scholar
Tambasco, N. et al. T2*-weighted MRI values correlate with motor and cognitive dysfunction in Parkinson’s disease. Neurobiol. Aging 80, 91–98 (2019).
Maass, F. et al. Cerebrospinal fluid iron-ferritin ratio as a potential progression marker for Parkinson’s disease. Mov. Disord. 36, 2967–2969 (2021).
Article CAS PubMed Google Scholar
Do Van, B. et al. Ferroptosis, a newly characterized form of cell death in Parkinson’s disease that is regulated by PKC. Neurobiol. Dis. 94, 169–178 (2016).
Tang, F. et al. Inhibition of ACSL4 alleviates Parkinsonism phenotypes by reduction of lipid reactive oxygen species. Neurotherapeutics 20, 1154–1166 (2023).
Article CAS PubMed PubMed Central Google Scholar
Shen, Q. Q. et al. Cell senescence induced by toxic interaction between alpha-synuclein and iron precedes nigral dopaminergic neuron loss in a mouse model of Parkinson’s disease. Acta Pharm. Sin. 45, 268–281 (2024).
Goodman, L. Alzheimer’s disease; a clinico-pathologic analysis of twenty-three cases with a theory on pathogenesis. J. Nerv. Ment. Dis. 118, 97–130 (1953).
Article CAS PubMed Google Scholar
Hallgren, B. & Sourander, P. The non-haemin iron in the cerebral cortex in Alzheimer’s disease. J. Neurochem. 5, 307–310 (1960).
Article CAS PubMed Google Scholar
Crapper McLachlan, D. R. et al. Intramuscular desferrioxamine in patients with Alzheimer’s disease. Lancet 337, 1304–1308 (1991).
Article CAS PubMed Google Scholar
Bartzokis, G. et al. In vivo evaluation of brain iron in Alzheimer’s disease and normal subjects using MRI. Biol. Psychiatry 35, 480–487 (1994).
Article CAS PubMed Google Scholar
Raven, E. P. et al. Increased iron levels and decreased tissue integrity in hippocampus of Alzheimer’s disease detected in vivo with magnetic resonance imaging. J. Alzheimers Dis. 37, 127–136 (2013).
Article CAS PubMed Google Scholar
Smith, M. A., Harris, P. L., Sayre, L. M. & Perry, G. Iron accumulation in Alzheimer disease is a source of redox-generated free radicals. Proc. Natl Acad. Sci. USA 94, 9866–9868 (1997).
Article CAS PubMed PubMed Central Google Scholar
Rottkamp, C. A. et al. Redox-active iron mediates amyloid-beta toxicity. Free Radic. Biol. Med. 30, 447–450 (2001).
Article CAS PubMed Google Scholar
Ayton, S. et al. Cerebral quantitative susceptibility mapping predicts amyloid-beta-related cognitive decline. Brain 140, 2112–2119 (2017).
Ayton, S. et al. Brain iron is associated with accelerated cognitive decline in people with Alzheimer pathology. Mol. Psychiatry 25, 2932–2941 (2020).
Article CAS PubMed Google Scholar
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