| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3069241 | Neurobiology of Disease | 2016 | 13 Pages |
•A438079 improved in vitro myelination of organotypic DRG cultures from CMT1A rats.•In CMT1A rats, A438079 increased muscle strength and number of myelinated axons.•A438079 reduced the SC differentiation defect in CMT1A rats.•Inhibition of the P2X7 receptor is well tolerated in CMT1A rats.•Antagonizing P2X7 may improve the clinical phenotype in the CMT1A neuropathy.
Charcot-Marie-Tooth 1A (CMT1A) is a demyelinating hereditary neuropathy for which pharmacological treatments are not yet available. An abnormally high intracellular Ca2+ concentration was observed in Schwann cells (SC) from CMT1A rats, caused by the PMP22-mediated overexpression of the P2X7 purinoceptor. The purpose of this study was to investigate the tolerability and therapeutic potential of a pharmacological antagonist of the P2X7 receptor (A438079) in CMT1A. A438079 ameliorated in vitro myelination of organotypic DRG cultures from CMT1A rats. Furthermore, we performed an experimental therapeutic trial in PMP22 transgenic and in wild-type rats. A preliminary dose-escalation trial showed that 3 mg/kg A438079 administered via intraperitoneal injection every 24 h for four weeks was well tolerated by wild type and CMT1A rats. Affected rats treated with 3 mg/kg A438079 revealed a significant improvement of the muscle strength, when compared to placebo controls. Importantly, histologic analysis revealed a significant increase of the total number of myelinated axons in tibial nerves. Moreover, a significant decrease of the hypermyelination of small caliber axons and a significant increase of the frequency and diameter of large caliber myelinated axons was highlighted. An improved distal motor latencies was recorded, whereas compound muscle action potentials (CMAP) remained unaltered. A438079 reduced the SC differentiation defect in CMT1A rats. These results show that pharmacological inhibition of the P2X7 receptor is well tolerated in CMT1A rats and represents a proof-of-principle that antagonizing this pathway may correct the molecular derangements and improve the clinical phenotype in the CMT1A neuropathy.
