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The Journal of Neurophysiology Vol. 81 No. 6 June 1999, pp. 2945-2955
Copyright ©1999 by the American Physiological Society
Department of Anatomy and Neurobiology, St. Louis University, St. Louis, Missouri 63104
Kogo, Naoki and
Michael Ariel.
Response Attenuation During Coincident Afferent Excitatory Inputs. J. Neurophysiol. 81: 2945-2955, 1999.
Response attenuation during coincident afferent excitatory inputs.
The linearity of the synaptic summation of two unitary excitatory synaptic events was investigated during whole cell recordings from retinal target neurons in an eye-attached isolated brain stem preparation. Pairs of unitary excitatory postsynaptic potentials (EPSPs) were evoked by bipolar stimulation electrodes that were directed to two distinct foci on the retinal surface based on
the visual receptive field boundaries. The interval between stimulation
of each retinal site was incremented by 0.5-1 ms to quantify the time
course of nonlinear summation using an exponential fit. Response
facilitation was never observed; however, the coincident arrival of
synaptic inputs caused a response attenuation in 26 of the 37 pairs
studied. Twelve of the 26 pairs had time constants of their attenuation
that were similar to the time constants of the decaying phases of the
first EPSPs of each pair. This suggests that the attenuation of these
12 pairs may be entirely due to voltage-dependent mechanisms, such as a
reduction in driving force or a change of the activity of
voltage-sensitive channels. On the other hand, the 14 other pairs had
their time constant of attenuation shorter than the time constants of
the decaying phase of the first EPSP. In fact, the attenuation time
constants were often closer to the time constants of the decaying
phases of the first excitatory postsynaptic currents of each pair. This
finding suggests that the attenuation of these 14 pairs involve a
shunting mechanism due to the opening of synaptic channels. The
presence of this conductance-dependent mechanism is supported by the
finding of asymmetric effects on the time course of attenuation when
the stimulation sequence was reversed. These results are discussed in
terms of the processing by neurons of coincident excitatory inputs onto
spatially distinct points of their dendritic trees.
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