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HDAC-6 inhibition ameliorates the early neuropathology in a mouse model of Krabbe disease.

Authors :
Braz SO
Morgado MM
Pereira MI
Monteiro AC
Golonzhka O
Jarpe M
Brites P
Sousa MM
Nogueira-Rodrigues J
Source :
Frontiers in molecular neuroscience [Front Mol Neurosci] 2023 Jul 27; Vol. 16, pp. 1231659. Date of Electronic Publication: 2023 Jul 27 (Print Publication: 2023).
Publication Year :
2023

Abstract

Introduction: In Krabbe disease (KD), mutations in β-galactosylceramidase (GALC), a lysosomal enzyme responsible for the catabolism of galactolipids, leads to the accumulation of its substrates galactocerebroside and psychosine. This neurologic condition is characterized by a severe and progressive demyelination together with neuron-autonomous defects and degeneration. Twitcher mice mimic the infantile form of KD, which is the most common form of the human disease. The Twitcher CNS and PNS present demyelination, axonal loss and neuronal defects including decreased levels of acetylated tubulin, decreased microtubule stability and impaired axonal transport.<br />Methods: We tested whether inhibiting the α-tubulin deacetylase HDAC6 with a specific inhibitor, ACY-738, was able to counteract the early neuropathology and neuronal defects of Twitcher mice.<br />Results: Our data show that delivery of ACY-738 corrects the low levels of acetylated tubulin in the Twitcher nervous system. Furthermore, it reverts the loss myelinated axons in the sciatic nerve and in the optic nerve when administered from birth to postnatal day 9, suggesting that the drug holds neuroprotective properties. The extended delivery of ACY-738 to Twitcher mice delayed axonal degeneration in the CNS and ameliorated the general presentation of the disease. ACY-738 was effective in rescuing neuronal defects of Twitcher neurons, stabilizing microtubule dynamics and increasing the axonal transport of mitochondria.<br />Discussion: Overall, our results support that ACY-738 has a neuroprotective effect in KD and should be considered as an add-on therapy combined with strategies targeting metabolic correction.<br />Competing Interests: OG and MJ were employed by Acetylon Pharmaceuticals Inc. The remaining 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.<br /> (Copyright © 2023 Braz, Morgado, Pereira, Monteiro, Golonzhka, Jarpe, Brites, Sousa and Nogueira-Rodrigues.)

Details

Language :
English
ISSN :
1662-5099
Volume :
16
Database :
MEDLINE
Journal :
Frontiers in molecular neuroscience
Publication Type :
Academic Journal
Accession number :
37588057
Full Text :
https://doi.org/10.3389/fnmol.2023.1231659