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The Journal of Neurophysiology Vol. 86 No. 2 August 2001, pp. 871-880
Copyright ©2001 by the American Physiological Society
Laboratory of Sensory Neuroscience, Department of Psychology, Carleton University, Ottawa, Ontario K1S 5B6, Canada
Zhang, Huiming and
Jack B. Kelly.
AMPA and NMDA Receptors Regulate Responses of Neurons in the
Rat's Inferior Colliculus. J. Neurophysiol. 86: 871-880, 2001. The contribution of
N-methyl-D-aspartate (NMDA) and AMPA receptors
to auditory responses in the rat's inferior colliculus was examined by
recording single-unit activity before, during, and after local
iontophoretic application of receptor-specific antagonists. Tone bursts
and sinusoidal amplitude modulated sounds were presented to one ear,
and recordings were made from the contralateral central nucleus of
inferior colliculus (ICC). The receptor specific antagonists,
(±)-3-(2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP) for
NMDA receptors and
1,2,3,4-tetrahydro-6-nitro-2,3-dioxo-benzo[f]quinoxaline-7-sulfonamide (NBQX) for AMPA receptors, were released at the recording site through a multi-barreled pipette. For most neurons, either CPP or NBQX
alone resulted in a reversible reduction in the number of action
potentials evoked by tonal stimulation. For neurons with an onset
response pattern, NBQX either completely eliminated or greatly reduced
the number of action potentials. CPP also reduced the number of action
potentials but had a less pronounced effect than NBQX. For neurons with
a sustained firing pattern, NBQX reduced the total number of action
potentials, but had a preferential effect on the early part (first
10-20 ms) of the response. CPP also resulted in a reduction in the
total number of action potentials, but had a more pronounced effect on
the later part (>20 ms) of the response. These results indicate that
both AMPA and NMDA receptors contribute to sound evoked excitatory
responses in the ICC. They have a selective influence on early and late
components of tone-evoked responses. Both receptor types are involved
in generating excitatory responses across a wide range of sound
pressure levels as indicated by rate level functions obtained before
and during drug application. In addition, both CPP and NBQX reduced
responses to sinusoidal amplitude modulated sounds. The synchrony of
firing to the modulation envelope as measured by vector strength at
different rates of modulation was not greatly affected by either CPP or
NBQX in spite of the decrease in firing rate.
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