Arginine butyrate per os protects mdx mice against cardiomyopathy, kyphosis and changes in axonal excitability. - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Neurobiology of Disease Année : 2014

Arginine butyrate per os protects mdx mice against cardiomyopathy, kyphosis and changes in axonal excitability.

Résumé

Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disease caused by lack of dystrophin, a sub-sarcolemmal protein, which leads to dramatic muscle deterioration. We studied in mdx mice, the effects of oral administration of arginine butyrate (AB), a compound currently used for the treatment of sickle cell anemia in children, on cardiomyopathy, vertebral column deformation and electromyographic abnormalities. Monthly follow-up by echocardiography from the 8th month to the 14th month showed that AB treatment protected the mdx mice against drastic reduction (20-23%) of ejection fraction and fractional shortening, and also against the ≈20% ventricular dilatation and 25% cardiac hypertrophy observed in saline-treated mdx mice. The phenotypic improvement was corroborated by the decrease in serum CK level and by better fatigue resistance. Moreover, AB treatment protected against the progressive spinal deformity observed in mdx mice, another similarity with DMD patients. The value of the kyphosis index in AB-treated mice reached 94% of the value in C57BL/10 mice. Finally, axonal excitability parameters such as the membrane resting potential, the threshold and amplitude of the action potential, the absolute and relative refractory periods and the supernormal and subnormal periods, recorded from caudal and plantar muscles in response to excitability tests, that were modified in saline-treated mdx mice were not significantly changed, compared with wild-type animals, in AB-treated mdx mice. All of these results suggest that AB could be a potential treatment for DMD patients.
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Dates et versions

hal-01443805 , version 1 (23-01-2017)

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Sara Vianello, Sophie Bouyon, Evelyne Benoit, Catherine Sebrié, Delphine Boerio, et al.. Arginine butyrate per os protects mdx mice against cardiomyopathy, kyphosis and changes in axonal excitability.. Neurobiology of Disease, 2014, 71, pp.325-33. ⟨10.1016/j.nbd.2014.08.023⟩. ⟨hal-01443805⟩
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