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The Journal of Neurophysiology Vol. 83 No. 3 March 2000, pp. 1592-1604
Copyright ©2000 by the American Physiological Society
1Neurological Sciences Institute, Oregon Health Sciences University, Portland, Oregon 97209; and 2Institute Alfred Fessard, Centre National de la Recherche Scientifique, 91190 Gif sur Yvette, France
Han, Victor Z.,
Kirsty Grant, and
Curtis C. Bell.
Rapid Activation of GABAergic Interneurons and Possible Calcium
Independent GABA Release in the Mormyrid Electrosensory Lobe. J. Neurophysiol. 83: 1592-1604, 2000. The primary afferent fibers from the electroreceptors of
mormyrid electric fish terminate centrally in the granular layer of the
electrosensory lobe (ELL). This study examines the excitatory and
inhibitory processes that take place in this layer using an in vitro
slice preparation and field potentials evoked by stimulation of primary
afferent fibers in the deep fiber layer of ELL. The postsynaptic
response to stimulation of the afferent fibers was still present after
blocking chemical transmission in three different ways: by adding
glutamate receptor antagonists to the medium, by substituting a
nominally calcium-free medium for normal medium, and by blocking
calcium channels with cadmium. Blockade of chemical transmission was
demonstrated by disappearance of control responses to parallel fiber
stimulation. The continued presence of a postsynaptic response in the
absence of chemical excitation is consistent with previous anatomic and
physiological evidence for electrical synapses between afferent fibers
and granular cells in ELL. Granular cell activation by primary afferent
fibers was followed by a powerful, short-latency inhibition mediated by
GABA and GABAA receptors, as indicated by a large increase
in the postsynaptic response to afferent fiber stimulation following
application of the GABAA receptor antagonist, bicuculline.
Bicuculline caused a marked increase of the postsynaptic response even
after chemical synaptic excitation had been blocked by glutamate
receptor antagonists, by a calcium-free medium, or by cadmium. Thus
activation of the inhibitory interneurons responsible for GABA release
did not require chemical excitation. Nonchemical excitation of the
inhibitory interneurons could be mediated either by electrical synapses
between afferent fibers and inhibitory interneurons, or by nonsynaptic activation of the large GABAergic terminals that are known to be
present on granular cells. The marked increase of the postsynaptic response caused by bicuculline in a calcium-free medium or in the
presence of cadmium suggests that the release of GABA by inhibitory terminals was not entirely dependent on calcium influx. This effect of
bicuculline on the postsynaptic response in a calcium-free medium or in
the presence of cadmium was markedly reduced by prior addition of the
GABA transporter antagonist, nipecotic acid. Thus calcium-independent
release of GABA may occur in ELL and may be partly dependent on
reversal of a GABA transporter. Rapid and powerful inhibition at the
first stage in the processing of electrosensory information could serve
to enhance the small differences in latency among afferent fibers that
appear to encode small differences in stimulus intensity.
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