Relationship between the nerve action potential and transmitter release from sympathetic postganglionic nerve terminals

At the skeletal neuromuscular junction, electrophysiological methods have provided much useful information about the mechanisms involved in the release of transmitter. At the autonomic neuroeffector junction it has not been possible to carry out similar studies. Here we report a method of extracellular recording which allows simultaneous measurement of both the nerve action potential and transmitter release from postganglionic sympathetic nerve terminals. We have confirmed that release is intermittent, but the importance of this new approach is that the relationship between the nerve terminal action potential and transmitter release can be studied unambiguously for the first time. Thus we are able to show unequivocally that intermittence is caused by a low probability of release in the invaded varicosity and not by failure of the action potential to invade the varicosity.     

Transmitter release from frog motor nerve terminals depends on motor unit size

It has been postulated that the success with which a motor nerve terminal competes for synaptic connections or the ability of an axon to maintain sprouts may depend on the support each terminal receives from its coma, presumably in the form of some substance(s) synthesized there. The support received by each terminal may in turn depend on the total number of terminals maintained by that soma, namely, motor unit size. We show here that when motor unit size is experimentally decreased, transmitter release from the terminals is markedly enhanced. This is consistent with the view that the extent of support from the soma may also influence the effectiveness of synaptic transmission.     

Action potentials must admit calcium to evoke transmitter release.

There are two hypotheses to explain how neurons release transmitter. The calcium hypothesis proposes that membrane depolarization is necessary only for opening calcium channels and increasing internal calcium concentration ([Ca2+]i) near membrane transmitter-release sites. These calcium ions trigger a transient release of neurotransmitter. The calcium-voltage hypothesis postulates that voltage induces a conformational change in a membrane protein rendering it sensitive to calcium such that, in the presence of high [Ca2+]i, depolarization directly triggers transmitter release. Here we report that when calcium influx is blocked by cobalt or manganese ions in a calcium-free Ringer, as measured with Fura-2, and [Ca2+]i is elevated by liberation from a caged calcium compound, transmitter release at the crayfish neuromuscular junction is unaffected by presynaptic action potentials. These results support the calcium hypothesis.