The 6-hydroxydopamine (6-OHDA) model of nigral injury in rats has been in use as a standard animal model of parkinsonism for many years. While earlier studies established the time course for loss of catecholamine histofluorescence or tyrosine hydroxylase immunostaining in the cell bodies and terminals, these alterations in phenotypic expression do not define the time course of morphologic degeneration. We have therefore used a silver impregnation method to characterize the time course and morphology of the degeneration of neurons in the nigrostriatal system. Abundant neuronal death was observed in substantia nigra pars compacta (SNpc) as early as 12 hours after nigral 6-OHDA injection, and prior to any evidence of striatal terminal degeneration. From 1 to 7 days neuron death was accompanied by striatal fibre degeneration. After 7 days, fibre degeneration was no longer seen, but identifiable neuron death continued at low levels for as long as 31 days, and stained amorphous material was present at 60 days. The morphologic pattern of cell death in the early phase was similar to that in the late phase, and included cytoplasmic silver deposits and dark staining of the nucleolus. At no time was the morphology of apoptosis observed. We conclude that neuron death is a progressive process following 6-OHDA lesion, with similar morphology throughout the course of degeneration.
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Univ South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R ChinaUniv South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R China
Jiang, Wu
Zou, Wei
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Univ South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R ChinaUniv South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R China
Zou, Wei
Hu, Min
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Univ South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R ChinaUniv South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R China
Hu, Min
Tian, Qing
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Univ South China, Hengyang Med Sch, Inst Neurosci, Hengyang Key Lab Neurodegenerat & Cognit Impairme, Hengyang, Hunan, Peoples R ChinaUniv South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R China
Tian, Qing
Xiao, Fan
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Univ South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R ChinaUniv South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R China
Xiao, Fan
Li, Min
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Univ South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R ChinaUniv South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R China
Li, Min
Zhang, Ping
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Univ South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R ChinaUniv South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R China
Zhang, Ping
Chen, Yong-Jun
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Univ South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R ChinaUniv South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R China
Chen, Yong-Jun
Jiang, Jia-Mei
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Univ South China, Affiliated Hosp 1, Hengyang Med Sch, Inst Neurol, Hengyang, Hunan, Peoples R ChinaUniv South China, Affiliated Nanhua Hosp, Hengyang Med Sch, Dept Neurol, Hengyang, Hunan, Peoples R China