Influence of β₂-adrenergic selective agonist formoterol on the motor unit of a mouse model of a congenital myasthenic syndrome with complete VAChT deletion

Autor(es):Mostrar menos -

Rossi, Leonardo ; Mota, Barbara I. ; Valadao, Priscila A. C. ; Magalhaes-Gomes, Matheus P. S. ; Oliveira, Bruna S. ; Guatimosim, Silvia ; Navegantes, Luiz C. C. ; Miranda, Aline S. ; Prado, Marco A. M. ; Prado, Vania F. ; Guatimosim, Cristina

• Tipo de documento: Artigo Científico
• Fonte: Neuropharmacology; v. 260, p. 11-pg., 2024-08-30.

Resumo

Congenital Myasthenic Syndromes (CMS) are a set of genetic diseases that affect the neuromuscular transmission causing muscular weakness. The standard pharmacological treatment aims at ameliorating the myasthenic symptom by acetylcholinesterase inhibitors. Most patients respond well in the short and medium term, however, over time the beneficial effects rapidly fade, and the efficacy of the treatment diminishes. Increasing evidence shows that beta(2)-adrenergic agonists can be a suitable choice for the treatment of neuromuscular disorders, including CMS, as they promote beneficial effects in the neuromuscular system. The exact mechanism on which they rely is not completely understood, although patients and animal models respond well to the treatment, especially over extended periods. Here, we report the use of the long-lasting specific beta(2)-adrenergic agonist formoterol in a myasthenic mouse model (mnVAChT-KD), featuring deletion of VAChT (Vesicular Acetylcholine Transporter) specifically in the alpha-motoneurons. Our findings demonstrate that formoterol treatment (300 mu g/kg/day; sc) for 30 days increased the neuromuscular junction area, induced skeletal muscle hypertrophy and altered fibre type composition in myasthenic mice. Interestingly, beta(2)-adrenergic agonists have shown efficacy even in the absence of ACh (acetylcholine). Our data provide important evidence supporting the potential of beta(2)-adrenergic agonists in treating neuromuscular disorders of pre-synaptic origin and characterized by disruptions in nerve-muscle communication, through a direct and beneficial action within the motor unit. (AU)

• Processo FAPESP: 18/10089-2 - Controle neural, hormonal e nutricional da autofagia
• Beneficiário: Isis Do Carmo Kettelhut
• Modalidade de apoio: Auxílio à Pesquisa - Temático