1. β2-Adrenergic Regulation of the Neuromuscular Transmission and Its Lipid-Dependent Switch.
- Author
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Gafurova CR, Tsentsevitsky AN, Fedorov NS, Khaziev AN, Malomouzh AI, and Petrov AM
- Subjects
- Animals, Membrane Microdomains metabolism, Membrane Microdomains drug effects, Mice, Male, Diaphragm drug effects, Diaphragm innervation, Diaphragm metabolism, Sphingomyelin Phosphodiesterase metabolism, Synaptic Vesicles metabolism, Synaptic Vesicles drug effects, Cholesterol metabolism, Exocytosis drug effects, Mice, Inbred C57BL, Neuromuscular Junction drug effects, Neuromuscular Junction metabolism, Synaptic Transmission drug effects, Receptors, Adrenergic, beta-2 metabolism
- Abstract
β2-Adrenoceptors (β2-ARs) are the most abundant subtype of adrenergic receptors in skeletal muscles. Their activation via a stabilization of postsynaptic architecture has beneficial effects in certain models of neuromuscular disorders. However, the ability of β2-ARs to regulate neuromuscular transmission at the presynaptic level is poorly understood. Using electrophysiological recordings and fluorescent FM dyes, we found that β2-AR activation with fenoterol enhanced an involvement of synaptic vesicles in exocytosis and neurotransmitter release during intense activity at the neuromuscular junctions of mouse diaphragm. This was accompanied by an improvement of contractile responses to phrenic nerve stimulation (but not direct stimulation of the muscle fibers) at moderate-to-high frequencies. β2-ARs mainly reside in lipid microdomains enriched with cholesterol and sphingomyelin. The latter is hydrolyzed by sphingomyelinases, whose upregulation occurs in many conditions characterized by muscle atrophy and sympathetic nerve hyperactivity. Sphingomyelinase treatment reversed the effects of β2-AR agonist on the neurotransmitter release and synaptic vesicle recruitment to the exocytosis during intense activity. Inhibition of G
i protein with pertussis toxin completely prevented the sphingomyelinase-mediated inversion in the β2-AR agonist action. Note that lipid raft disrupting enzyme cholesterol oxidase had the same effect on β2-AR agonist-mediated changes in neurotransmission as sphingomyelinase. Thus, β2-AR agonist fenoterol augmented recruitment and release of synaptic vesicles during intense activity in the diaphragm neuromuscular junctions. Sphingomyelin hydrolysis inversed the effects of β2-AR agonist on neurotransmission probably via switching to Gi protein-dependent signaling. This phenomenon may reflect a dependence of the β2-AR signaling on lipid raft integrity in the neuromuscular junctions., (© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)- Published
- 2024
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