Adenosine promotes endplate nAChR channel activity in adult mouse skeletal muscle fibres via low affinity P1 receptors
Self archived versionfinal draft
MetadataShow full item record
CitationBernareggi, Annalisa. Ren, Elisa. Giniatullin, Arthur. Luin, Elisa. Sciancalepore, Marina. Giniatullin, Rashid. Lorenzon, Paola. (2018). Adenosine promotes endplate nAChR channel activity in adult mouse skeletal muscle fibres via low affinity P1 receptors. NEUROSCIENCE, 383, 1-11. 10.1016/j.neuroscience.2018.04.044.
Adenosine is a powerful modulator of skeletal neuromuscular transmission, operating via inhibitory or facilitatory purinergic-type P1 receptors. To date, studies have been focused mainly on the effect of adenosine on presynaptic P1 receptors controlling transmitter release. In this study, using two-microelectrode voltage-clamp and single-channel patch-clamp recording techniques, we have explored potential postsynaptic targets of adenosine and their modulatory effect on nicotinic acetylcholine receptor (nAChR)-mediated synaptic responses in adult mouse skeletal muscle fibers in vitro.
In the whole-mount neuromuscular junction (NMJ) preparation, adenosine (100 μM) significantly reduced the frequency of the miniature endplate currents (MEPCs) and slowed their rising and decay time. Consistent with a postsynaptic site of action, adenosine and the potent P1 receptor agonist NECA significantly increased the open probability, the frequency and the open time of single nAChR channels, recorded at the endplate region. Using specific ligands for the P1 receptor subtypes, we found that the low-affinity P1 receptor subtype A2B was responsible for mediating the effects of adenosine on the nAChR channel openings. Our data suggest that at the adult mammalian NMJ, adenosine acts not only presynaptically to modulate acetylcholine transmitter release, but also at the postsynaptic level, to enhance the activity of nAChRs. Our findings open a new scenario in understanding of purinergic regulation of nAChR activity at the mammalian endplate region.
Subjectsadenosine adult skeletal muscle MEPC nAChR P1 receptor
Link to the original itemhttp://dx.doi.org/10.1016/j.neuroscience.2018.04.044
- Terveystieteiden tiedekunta