posted on 2020-12-15, 16:35authored byGiulio Auciello, Annalise Di Marco, Odalys Gonzalez Paz, Savina Malancona, Steven Harper, Maria Beconi, Ilaria Rossetti, Alina Ciammaichella, Paola Fezzardi, Andrea Vecchi, Elena Bracacel, Daniel Cicero, Edith Monteagudo, Daniel Elbaum
Mutations in the human PANK2 gene
are implicated in neurodegenerative
diseases such as pantothenate kinase-associated neurodegeneration
(PKAN) and result in low levels of coenzyme-A (CoA) in the CNS due
to impaired production of phosphopantothenic acid (PPA) from vitamin
B5. Restoration of central PPA levels by delivery of exogenous PPA
is a recent strategy to reactivate CoA biosynthesis in PKAN patients.
Fosmetpantotenate is an oral PPA prodrug. We report here the development
of a new PANk2–/– knockout model that allows
CoA regeneration in brain cells to be evaluated and describe two new
series of cyclic phosphate prodrugs of PPA capable of regenerating
excellent levels of CoA in this system. A proof-of-concept study in
mouse demonstrates the potential of this new class of prodrugs to
deliver PPA to the brain following oral administration and confirms
incorporation of the prodrug-derived PPA into CoA.