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Probabilistic secretion of quanta from nerve terminals in avian ciliary ganglia modulated by adenosine.
Author(s) -
Bennett M R,
Ho S
Publication year - 1991
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1991.sp018722
Subject(s) - excitatory postsynaptic potential , adenosine , chemistry , postsynaptic potential , ciliary ganglion , inhibitory postsynaptic potential , hyperpolarization (physics) , biophysics , acetylcholine , medicine , neurotransmission , endocrinology , ganglion , neuroscience , biology , biochemistry , receptor , organic chemistry , nuclear magnetic resonance spectroscopy
1. The effects of adenosine on the probability of secretion of acetylcholine quanta and on presynaptic and postsynaptic action potentials was examined in the post‐hatched avian ciliary ganglion. 2. Adenosine (20 microM) reduced the average size of the excitatory postsynaptic potential (EPSP) by 33%. This was due to a decrease in quantal content of the EPSP (m). The effect was blocked by theophylline (50 microM). 3. Adenosine deaminase (2.5 i.u./ml) increased the size of the EPSP by 70%, suggesting that endogenous adenosine modulates synaptic transmission in the ciliary ganglion. However, theophylline (20‐100 microM) did not affect the EPSP in a low [Ca2+]o of 1 mM and high [Mg2+]o of 6 mM. 4. Plateau‐type action potentials with a large calcium component were generated in the ciliary neurones by bathing the ganglion in tetraethylammonium ions (TEA, 10 mM). Adenosine (20 microM) reduced the duration of these action potentials on short exposures (less than 20 min) but increased the duration on longer exposure (greater than 30 min). Adenosine did not affect the normal action potential recorded in the absence of TEA. 5. Adenosine (20 microM) hyperpolarized the nerve terminal and as a consequence increased the size of the presynaptic action potential and reduced its after‐hyperpolarization. 6. Plateau‐type action potentials with a large calcium component were generated in the nerve terminals using TEA (10 mM). The duration of these action potentials was significantly reduced by adenosine (20 microM). 7. Adenosines action on nerve terminals, to hyperpolarize the membrane and reduce calcium influx, may contribute to its effect in reducing m of the EPSP.