Neuronal haemoglobin is reduced in alzheimer's disease, argyrophilic grain disease, parkinson's disease, and dementia with lewy bodies

Previous studies have demonstrated the presence of hemoglobin α-chain and β-chain in neurons of the rodent and human brain thus indicating that hemoglobin is a normal component of nerve cells and that hemoglobin may play a role in intraneuronal oxygen homeostasis. Progressing with these studies, hem...

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Bibliographic Details
Authors: Ferrer, Isidro (Ferrer Abizanda), Gómez, Ana, Carmona Murillo, Margarita, Huesa, Gema, Porta, Sílvia, Riera i Codina, Miquel, Biagioli, Marta, Gustincich, Stefano, Aso Pérez, Ester
Format: article
Status:Published version
Publication Date:2011
Country:España
Institution:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repository:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/172902
Online Access:https://hdl.handle.net/2445/172902
Access Level:Open access
Keyword:Malaltia d'Alzheimer
Metabolisme
Hemoglobina
Demència amb cossos de Lewy
Neurones
Malaltia de Parkinson
Alzheimer's disease
Metabolism
Hemoglobin
Lewy body dementia
Neurons
Parkinson's disease
Description
Summary:Previous studies have demonstrated the presence of hemoglobin α-chain and β-chain in neurons of the rodent and human brain thus indicating that hemoglobin is a normal component of nerve cells and that hemoglobin may play a role in intraneuronal oxygen homeostasis. Progressing with these studies, hemoglobin expression has been examined in selected cell population in the brains of Alzheimer's disease (AD), argyrophilic grain disease (AGD), Parkinson's disease (PD) and Dementia with Lewy bodies (DLB). Double labeling immunofluorescence and confocal microscopy revealed reduced hemoglobin α-chain and β-chain in practically all neurons with small amounts of granular or punctuate hyperphosphorylated tau deposits and in neurons with tangles in the hippocampus and frontal cortex in AD and in the hippocampus in AGD; in ballooned neurons containing αB-crystallin in the amygdala in AD and AGD; and in about 80% of neurons with punctuate α-synuclein deposits and in neurons with Lewy bodies in the substantia nigra pars compacta and in vulnerable neurons of the medulla oblongata in PD and DLB; and in neurons with Lewy bodies in the frontal cortex in DLB. Hemoglobin immunoreactivity was also observed in the core of neuritic plaques and in diffuse plaques, but not in dystrophic neurites. Loss of hemoglobin was specific as neuroglobin was present equally in neurons with and without abnormal protein inclusions, and erythropoietin receptor was expressed equally in neurons without and in neurons with abnormal protein aggregates in AD, AGD, PD, and DLB.