Arginine ameliorates motor and survival deficits in MFN2-Deficient Drosophila models
Charcot-Marie-Tooth disease type 2 A (CMT2A) is an inherited axonal neuropathy linked to mutations in MFN2, a key regulator of mitochondrial dynamics. Currently, no effective drug therapies exist. l-arginine has shown promise in treating mitochondrial disorders, though its effect on MFN2-associated neuropathy remains uncertain. To investigate this, we used Drosophila models with the neuron-specific knockdown of Marf, the fly ortholog of MFN2, employing a temporally controlled GAL4/UAS system. Flies were administered different doses of l-arginine to examine its influence on motor ability and lifespan. To evaluate responses under mitochondrial stress, flies were also treated with rotenone, a mitochondrial complex I inhibitor. l-arginine markedly improved climbing performance under baseline conditions and extended lifespan under both baseline and stress conditions. However under rotenone-induced mitochondrial stress, high-dose l-arginine improved survival without a corresponding improvement in locomotor performance. These results support a neuroprotective role for l-arginine in MFN2-deficient Drosophila, possibly through effects on mitochondrial dynamics involving complex I. l-arginine may hold therapeutic promise for CMT2A, meriting further investigation in vertebrate models.
Authors
- Yusuke Sakiyama (ORCID: https://orcid.org/0000-0003-0691-1705)
- Takahiro Hobara (ORCID: https://orcid.org/0009-0001-2900-182X)
- Satoshi Nozuma (ORCID: https://orcid.org/0000-0002-4909-7769)
- Yuji Okamoto (ORCID: https://orcid.org/0009-0009-9892-0828)
- Fumikazu Kojima (ORCID: https://orcid.org/0009-0004-7867-2285)
- Risa Nagatomo
- Chikashi Yano (ORCID: https://orcid.org/0009-0002-1468-3415)
- Hiroshi Takashima
- Jun-Hui Yuan
- Yujiro Higuchi
- Masahiro Ando
- Yu Hiramatsu
- Akiko Yoshimura
Institutions
- Kagoshima University (JP)
- Kagoshima Medical Center (JP)
Publication Details
- Journal
- Neurotherapeutics
- Published
- 2026-04-01
- DOI
- https://doi.org/10.1016/j.neurot.2026.e00900
- Primary Topic
- Hereditary Neurological Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Kagoshima University
- Japan Agency for Medical Research and Development
- Japan Society for the Promotion of Science
- Research Committee for Ataxic Disease