Variable effects of omaveloxolone (RTA408) on primary fibroblasts with mitochondrial defects.

Omavleoxolone RTA408 Parkinson’s disease ROS fibroblasts mitochondria mitochondrial disease

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
Historique:
received: 06 03 2022
accepted: 07 07 2022
entrez: 29 8 2022
pubmed: 30 8 2022
medline: 30 8 2022
Statut: epublish

Résumé

Omaveloxolone (RTA408) is a second-generation oleanane triterpenoid Nrf2 inducer with antioxidant and anti-inflammatory properties and was reported to improve mitochondrial bioenergetics. It is currently being tested in medical trials for Friedrich ataxia, a genetic, multi-organ disease involving mitochondrial dysfunction. Thus, omaveloxolone could potentially be beneficial for additional disorders involving mitochondrial dysfunction. To this end, we investigated its effect on primary fibroblasts derived from patients with mitochondrial complex I deficiency, mitochondrial cytochrome oxidase deficiency, and two recessive forms of Parkinson's disease. Patients and control cells were incubated in the presence or absence of 50 nM omaveloxolone for 72 h prior to measurements. Generally, growth on galactose medium and ATP production were unaltered. Mitochondrial membrane potential was slightly but significantly decreased, while reactive oxygen species (ROS) production was variably decreased. Mitochondrial mass and mitochondrial DNA (mtDNA) contents were significantly increased in the patient's cells. These results were partially confirmed by the results of oxygen consumption studies which disclosed increased maximal oxygen consumption rates in most cells and increased energy status in all treated cells. Further investigation is required to explore the precise effect of omaveloxolone on mitochondrial function in disease.

Identifiants

pubmed: 36032663
doi: 10.3389/fmolb.2022.890653
pii: 890653
pmc: PMC9411646
doi:

Types de publication

Journal Article

Langues

eng

Pagination

890653

Informations de copyright

Copyright © 2022 Zighan, Arkadir, Douiev, Keller, Miller and Saada.

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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Auteurs

Madleen Zighan (M)

Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

David Arkadir (D)

Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Department of Neurology, Hadassah Medical Center, Jerusalem, Israel.

Liza Douiev (L)

Department of Genetics, Hadassah Medical Center, Jerusalem, Israel.
Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Guy Keller (G)

Department of Genetics, Hadassah Medical Center, Jerusalem, Israel.
Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Department of Neurology, Hadassah Medical Center, Jerusalem, Israel.

Chaya Miller (C)

Department of Genetics, Hadassah Medical Center, Jerusalem, Israel.

Ann Saada (A)

Department of Genetics, Hadassah Medical Center, Jerusalem, Israel.
Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Classifications MeSH