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Inhibition of glutamate dehydrogenase as a new therapeutic approach in DMD
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European and Chinese researchers have focused on the glutamate pathway as a possible therapeutic target in Duchenne muscular dystrophy (DMD):
- this molecule plays an important role in the presynaptic endings of neuromuscular junctions,
- pharmacological inhibition of the enzymeProtéine capable d’activer une réaction biochimique précise. GLUD-1 (glutamate dehydrogenase 1) by compound R162 was analysed in mdx mice, a model of DMD,
- the compound R162 was shown to remodel neuromuscular junctions and improve muscle performance in mice.
This is the first time it has been studied in the mouse model of DMD, as a prelude to possible clinical trials.