Excitatory amino acid receptor-mediated transmission in geniculocortical and intracortical pathways within visual cortex
L. J. Larson-Prior, P. S. Ulinski and N. T. Slater Department of Physiology, Northwestern University Medical School, Chicago, Illinois. 1. A preparation of turtle (Chrysemys picta and Pseudemys scripta) brain in which the integrity of the intracortical and geniculocortical pathways in visual cortex...
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Veröffentlicht in: | Journal of neurophysiology 1991-07, Vol.66 (1), p.293-306 |
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Zusammenfassung: | L. J. Larson-Prior, P. S. Ulinski and N. T. Slater
Department of Physiology, Northwestern University Medical School, Chicago, Illinois.
1. A preparation of turtle (Chrysemys picta and Pseudemys scripta) brain in
which the integrity of the intracortical and geniculocortical pathways in
visual cortex are maintained in vitro has been used to differentiate the
excitatory amino acid (EAA) receptor subtypes involved in geniculocortical
and intracortical synapses. 2. Stimulation of the geniculocortical fibers
at subcortical loci produces monosynaptic excitatory postsynaptic
potentials (EPSPs) in visual cortical neurons. These EPSPs are blocked by
the broad-spectrum EAA receptor antagonist kynurenate (1-2 mM) and the
non-N-methyl-D-aspartate (NMDA) antagonist 6,
7-dinitroquinoxaline-2,3-dione (DNQX, 10 microM), but not by the NMDA
antagonist D,L-2-amino-5-phosphonovalerate (D,L-AP-5, 100 microM). These
results indicate that the geniculocortical EPSP is mediated by EAAs that
access principally, if not exclusively, EAA receptors of the non-NMDA
subtypes. 3. Stimulation of intracortical fibers evokes compound EPSPs that
could be resolved into three components differing in latency to peak. The
component with the shortest latency was not affected by any of the
EAA-receptor antagonists tested. The second component, of intermediate
latency, was blocked by kyurenate and DNQX but not by D,L-AP-5. The
component of longest latency was blocked by kynurenate and D,L-AP-5, but
not by DNQX. These results indicate that the compound intracortical EPSP is
comprised of three pharmacologically distinct components that are mediated
by an unknown receptor, by quisqualate/kainate, and by NMDA receptors,
respectively. 4. Repetitive stimulation of intracortical pathways at 0.33
Hz produces a dramatic potentiation of the late, D,L-AP-5-sensitive
component of the intracortical EPSP. 5. These experiments lead to a
hypothesis about the subtypes of EAA receptors that are accessed by the
geniculocortical and intracortical pathways within visual cortex. |
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ISSN: | 0022-3077 1522-1598 |
DOI: | 10.1152/jn.1991.66.1.293 |