Targeting Chelatable Iron as a Therapeutic Modality in Parkinson's Disease
Author(s) -
David Devos,
Caroline Moreau,
Jean Christophe Devedjian,
Jérôme Kluza,
Maud Pétrault,
Charlotte Laloux,
Aurélie Jonneaux,
Gilles Ryckewaert,
Guillaume Garçon,
Nathalie Rouaix,
Alain Duhamel,
P. Jissendi,
Kathy Dujardin,
F. Auger,
Laura Ravasi,
Lucie Hopes,
Guillaume Grolez,
Wance Firdaus,
Bernard Sablonnière,
Isabelle Strubi-Vuillaume,
Noël Zahr,
A. Destée,
JeanChristophe Corvol,
Dominik Pöltl,
Marcel Leist,
Christian Rosé,
Luc Defebvre,
Philippe Marchetti,
Z. Ioav Cabantchik,
Régis Bordet
Publication year - 2013
Publication title -
antioxidants and redox signaling
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.277
H-Index - 190
eISSN - 1557-7716
pISSN - 1523-0864
DOI - 10.1089/ars.2013.5593
Subject(s) - deferiprone , substantia nigra , oxidative stress , dopamine , parkinson's disease , striatum , deferasirox , medicine , placebo , deferoxamine , clinical trial , disease , pathology , gastroenterology , pharmacology , alternative medicine , thalassemia
The pathophysiological role of iron in Parkinson's disease (PD) was assessed by a chelation strategy aimed at reducing oxidative damage associated with regional iron deposition without affecting circulating metals. Translational cell and animal models provided concept proofs and a delayed-start (DS) treatment paradigm, the basis for preliminary clinical assessments.
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