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Identification of a Novel 1,4,8-Triazaphenanthrene Derivative as a Neuroprotectant for Dopamine Neurons Vulnerable in Parkinson's Disease.
Le Douaron, Gael; Ferrié, Laurent; Sepulveda-Diaz, Julia E; Séon-Méniel, Blandine; Raisman-Vozari, Rita; Michel, Patrick P; Figadère, Bruno.
Afiliação
  • Le Douaron G; BioCIS, Université Paris-Sud, CNRS, Université Paris-Saclay, 92290 Châtenay-Malabry, France.
  • Ferrié L; Institut du Cerveau et de la Moelle, Sorbonne Universités, Université Pierre et Marie Curie Paris 06, INSERM U1127, CNRS UMR7225, 75013 Paris, France.
  • Sepulveda-Diaz JE; BioCIS, Université Paris-Sud, CNRS, Université Paris-Saclay, 92290 Châtenay-Malabry, France.
  • Séon-Méniel B; Institut du Cerveau et de la Moelle, Sorbonne Universités, Université Pierre et Marie Curie Paris 06, INSERM U1127, CNRS UMR7225, 75013 Paris, France.
  • Raisman-Vozari R; BioCIS, Université Paris-Sud, CNRS, Université Paris-Saclay, 92290 Châtenay-Malabry, France.
  • Michel PP; Institut du Cerveau et de la Moelle, Sorbonne Universités, Université Pierre et Marie Curie Paris 06, INSERM U1127, CNRS UMR7225, 75013 Paris, France.
  • Figadère B; Institut du Cerveau et de la Moelle, Sorbonne Universités, Université Pierre et Marie Curie Paris 06, INSERM U1127, CNRS UMR7225, 75013 Paris, France.
ACS Chem Neurosci ; 8(6): 1222-1231, 2017 06 21.
Article em En | MEDLINE | ID: mdl-28140556
ABSTRACT
Parkinson's disease (PD) is a chronic degenerative disorder characterized by typical motor symptoms caused by the death of dopamine (DA) neurons in the midbrain and ensuing shortage of DA in the striatum, at the level of nerve terminals. No curative treatment is presently available for PD in clinical practice. In our search for neuroprotectants in PD, we generated new 1,4,8-triazaphenanthrenes by combining 6-endo-dig-cycloisomerization of propargylquinoxalines and Suzuki or Sonogashira cross-coupling reactions. Neuroprotection assessment of newly synthesized 1,4,8-triazaphenanthrenes in a PD cellular model resulted in the discovery of a new hit compound PPQ (5m). Neuroprotection by 5m was concentration-dependent and the result of a combined effect on intracellular calcium release channels and astroglial cells. Of interest, 5m also counteracted DA cell loss in a mouse model of PD, making this molecule a promising candidate for PD treatment.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Neuroprotetores / Neurônios Dopaminérgicos / Antiparkinsonianos Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fármacos Neuroprotetores / Neurônios Dopaminérgicos / Antiparkinsonianos Idioma: En Ano de publicação: 2017 Tipo de documento: Article