Journal of Neuroscience, Vol 10, 1769-1778, Copyright © 1990 by Society for Neuroscience
Physiological differences between strong and weak frog neuromuscular junctions: a study involving tetanic and posttetanic potentiation
PA Pawson and AD Grinnell
Jerry Lewis Neuromuscular Research Center, UCLA School of Medicine 90024.
This paper describes the extent of release and terminal variability among
normal frog sartorius neuromuscular junctions and seeks physiological
correlates for these differences. Terminal length varied over approximately
a 10-fold range, quantal content and release per unit terminal length
("release efficacy") over much larger ranges. For purposes of comparison of
different junctions, release efficacy in a Ringer's containing 0.25 mM Ca2+
was determined in all cases. In a Ringer's containing 0.1 mM Ca2+, tetanic
stimulation causes a buildup of evoked release and of miniature endplate
potential (mEPP) frequency. The mEPP frequency at the end of the tetanus is
proportional to the evoked release level. Following the tetanus, the mEPP
frequency declines in a multiexponential fashion, with the 2 longest decay
phases, representing augmentation and posttetanic potentiation (PTP), both
having time constants that are positively linearly correlated with the
synaptic release efficacy. Longer or higher-frequency tetanic stimulation
resulted in a longer time course of decay of mEPP frequency. In a
Ca2(+)-free/EGTA Ringer's, tetanic stimulation causes no evoked release,
but does lead to an increased mEPP frequency, presumably due to a buildup
of free Ca2+ displaced from internal stores by the Na+ influx. Following
the tetanus, the mEPP frequency declines to resting level with a time
constant that is essentially the same for all junctions, regardless of
their release efficacy in Ca2(+)- containing Ringer's. These findings
indicate that stronger terminals have a greater influx of Ca2+ per unit
length during action potential invasion, but that in the absence of
external Ca2+, tetanic stimulation results in comparable release of Ca2+
from internal stores in all terminals and comparable accumulation of Ca2+
in some large compartment, the subsequent emptying of which determines the
time course of PTP.