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A 6-hydroxydopamine-induced selective parkinsonian rat model.
Perese, D A; Ulman, J; Viola, J; Ewing, S E; Bankiewicz, K S.
Afiliação
  • Perese DA; Surgical Neurology Branch, NINCDS, Bethesda, MD 20892.
Brain Res ; 494(2): 285-93, 1989 Aug 14.
Article em En | MEDLINE | ID: mdl-2528389
ABSTRACT
Previous parkinsonian rat models have generally been characterized by unilateral destruction of both the nigrostriatal pathway and the mesolimbic pathway using the neurotoxin 6-hydroxydopamine (6-OHDA). We created a hemiparkinsonian model in which there is 6-OHDA-induced destruction of the dopaminergic nigrostriatal pathway but sparing of the dopaminergic mesolimbic pathway. This resulted in reproducible, quantifiable rotational behavior in response to either amphetamine or apomorphine and a near total depletion of dopamine in the striatum ipsilateral to the lesion with a dorsolateral distribution of supersensitive dopaminergic D2 receptors. This model parallels the MPTP (1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine)-induced hemiparkinsonian model in primates and more closely approximates the extent of neurodegeneration seen in human idiopathic Parkinson's disease than previous parkinsonian rat models. It may therefore prove a convenient model for studying the recently reported phenomenon of sprouting from host dopaminergic neurons following tissue implantation.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson Secundária / Comportamento Estereotipado / Receptores Dopaminérgicos / Modelos Animais de Doenças / Hidroxidopaminas / Lateralidade Funcional / Sistema Límbico Limite: Animals Idioma: En Revista: Brain Res Ano de publicação: 1989 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Parkinson Secundária / Comportamento Estereotipado / Receptores Dopaminérgicos / Modelos Animais de Doenças / Hidroxidopaminas / Lateralidade Funcional / Sistema Límbico Limite: Animals Idioma: En Revista: Brain Res Ano de publicação: 1989 Tipo de documento: Article