A Drug Combination Rescues Frataxin-Dependent Neural and Cardiac Pathophysiology in FA Models.
Dimethyl fumarate (DMF)
Frataxin (FXN)
Friedreich’s Ataxia (FA)
Mitochondrial membrane potential (ΔΨm)
Reactive Oxygen species (ROS)
Resveratrol (Resv)
Journal
Frontiers in molecular biosciences
ISSN: 2296-889X
Titre abrégé: Front Mol Biosci
Pays: Switzerland
ID NLM: 101653173
Informations de publication
Date de publication:
2022
2022
Historique:
received:
07
12
2021
accepted:
17
03
2022
entrez:
6
6
2022
pubmed:
7
6
2022
medline:
7
6
2022
Statut:
epublish
Résumé
Friedreich's ataxia (FA) is an inherited multisystemic neuro- and cardio-degenerative disorder. Seventy-four clinical trials are listed for FA (including past and present), but none are considered FDA/EMA-approved therapy. To date, FA therapeutic strategies have focused along two main lines using a single-drug approach: a) increasing frataxin and b) enhancing downstream pathways, including antioxidant levels and mitochondrial function. Our novel strategy employed a combinatorial approach to screen approved compounds to determine if a combination of molecules provided an additive or synergistic benefit to FA cells and/or animal models. Eight single drug molecules were administered to FA fibroblast patient cells: nicotinamide riboside, hemin, betamethasone, resveratrol, epicatechin, histone deacetylase inhibitor 109, methylene blue, and dimethyl fumarate. We measured their individual ability to induce
Identifiants
pubmed: 35664670
doi: 10.3389/fmolb.2022.830650
pii: 830650
pmc: PMC9160322
doi:
Types de publication
Journal Article
Langues
eng
Pagination
830650Commentaires et corrections
Type : ErratumIn
Informations de copyright
Copyright © 2022 Abeti, Jasoliya, Al-Mahdawi, Pook, Gonzalez-Robles, Hui, Cortopassi and Giunti.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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