The immunophilin ligand GPI-1046 does not have neuroregenerative effects in MPTP-treated monkeys

Jamie L. Eberling, Phillip Pivirotto, John Bringas, Joseph P. Steiner, Jeffrey H. Kordower, Yaping Chu, Marina E. Emborg, Krzysztof S. Bankiewicz

Research output: Contribution to journalArticle

Abstract

Nonimmunosuppressant immunophilin ligands have been shown to have neurotrophic properties in rodent models of Parkinson's disease (PD), although little is known about the effects of these ligands in primates. The immunophilin ligand, GPI-1046, promotes the regeneration of dopamine (DA) cells in association with functional recovery in rodent models. We explored the regenerative effects of GPI-1046 in an MPTP primate model of PD. We used single photon emission computed tomography (SPECT) and the DA transporter tracer (DAT), [123I]β-CIT, to evaluate DAT density and clinical recovery before and after treatment with GPI-1046 or vehicle. Subsequent histological studies were also performed. No effects of GPI-1046 were found on any of these measures. These findings show that GPI-1046 does not have regenerative effects in MPTP-treated primates and suggest that there may be species differences with respect to the trophic effects of GPI-1046 on nigrostriatal DA neurons.

Original languageEnglish (US)
Pages (from-to)236-242
Number of pages7
JournalExperimental Neurology
Volume178
Issue number2
DOIs
StatePublished - Jan 1 2002

Keywords

  • Dopamine transporter
  • GPI-1046
  • Immunophilin
  • MPTP
  • Parkinson's disease
  • Regeneration
  • SPECT

ASJC Scopus subject areas

  • Neurology
  • Developmental Neuroscience

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  • Cite this

    Eberling, J. L., Pivirotto, P., Bringas, J., Steiner, J. P., Kordower, J. H., Chu, Y., Emborg, M. E., & Bankiewicz, K. S. (2002). The immunophilin ligand GPI-1046 does not have neuroregenerative effects in MPTP-treated monkeys. Experimental Neurology, 178(2), 236-242. https://doi.org/10.1006/exnr.2002.8023