Microglial activation is not prevented by tacrolimus but dopamine neuron damage is reduced in a rat model of Parkinson's disease progression

Ann K. Wright, Clare Miller, Maya Williams, Gordon Arbuthnott

Research output: Contribution to journalArticlepeer-review

Abstract

A progressive model of Parkinson's disease has been recently developed in the rat where a unilateral excitotoxic injection into the globus pallidus leads to a gradual loss of dopaminergic neurons in the ipsilateral substantia nigra. over a period of at least 6 weeks. In this model microglial activation is observed in the ipsilateral substantia. nigra 3 weeks after the lesion and could contribute to neuronal death at this time. The immunosuppressant drug tacrolimus (FK506) reduces dopamine cell death at 3 weeks following a globus pallidus lesion, but not thereafter. Tacrolimus-mediated neuroprotection could result from suppression of microglial activation but the microglial activation at three weeks post-lesion was not much reduced. Microglial activation was observed even in the apparent absence of neuronal death, prompting the suggestion that tacrolimus may prevent, or at least delay, the release of toxic cytokines from activated microglia. By 6 weeks after the GP lesion, even this mechanism fails to protect the dopamine cells from damage. (C) 2008 Elsevier B.V. All rights reserved.

Original languageEnglish
Pages (from-to)78-86
Number of pages9
JournalBrain Research
Volume1216
DOIs
Publication statusPublished - 24 Jun 2008

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