Effects of adenosine on Ca2+ entry in the nerve terminal of the frog neuromuscular junction

• Published in: Canadian journal of physiology and pharmacology Vol. 77; no. 9; pp. 707 - 714
• Main Authors: ROBITAILLE, R, THOMAS, S, CHARLTON, M. P
• Format: Conference Proceeding Journal Article
• Language: English
• Published: Ottawa, ON National Research Council of Canada 01.09.1999; Canadian Science Publishing NRC Research Press
• Subjects: Adenosine; Adenosine - pharmacology; Animals; Biological and medical sciences; Calcium; Calcium - metabolism; Frogs; Fundamental and applied biological sciences. Psychology; Hippocampus - drug effects; Hippocampus - metabolism; Muscles; Nervous system; Neuromuscular Junction - drug effects; Neuromuscular Junction - metabolism; Peripheral Nerves - drug effects; Peripheral Nerves - metabolism; Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ; Rana pipiens; Schwann Cells - drug effects; Schwann Cells - metabolism; Synapses; Synapses - drug effects; Vertebrates: nervous system and sense organs; Signal transduction; Vertebrata; Adenosine; Nerve ending; Calcium; Synaptic transmission; Frog; Amphibia; Synaptic depression; Salientia; Neuromuscular junction
• ISSN: 0008-4212; 1205-7541
• DOI: 10.1139/cjpp-77-9-707

This study aimed to test whether nerve-evoked and adenosine-induced synaptic depression are due to reduction in Ca2+ entry in nerve terminals of the frog neuromuscular junction. Nerve terminals were loaded with the fluorescent Ca2+ indicator fluo 3 (fluo 3-AM) or loaded with dextran-coupled Ca2+ green-1 transported from the cut end of the nerve. Adenosine (10-50 microM) did not change the resting level of Ca2+ in the presynaptic terminal, whereas it induced large Ca2+ responses in perisynaptic Schwann cells, indicating that adenosine was active and might have induced changes in the level of Ca2+ in the nerve terminal. Ca2+ responses in nerve terminals could be induced by nerve stimulation (0.5 or 100 Hz for 100 ms) over several hours. In the presence of adenosine (10 microM), the size and duration of the nerve-evoked Ca2+ responses were unchanged. When extracellular Ca2+ concentration was lowered to produce the same reduction in transmitter release as the application of adenosine, Ca2+ responses induced by nerve stimulations were reduced by 40%. This indicates that changes in Ca2+ responsible for the decrease in release should have been detected if the mechanism of adenosine depression involved partial block of Ca2+ influx. Ca2+ responses evoked by prolonged high frequency trains of stimuli (50 Hz for 10 or 30 s), which caused profound depression of transmitter release, were sustained during the whole duration of the stimulation, and adenosine had no effect on these responses. These data indicate that neither adenosine induced synaptic depression nor stimulation-induced synaptic depression are caused by reductions in Ca2+ entry into the presynaptic terminal in the frog neuromuscular junction.