Unitary EPSCs of corticogeniculate fibers in the rat dorsal lateral geniculate nucleus in vitro.

To investigate unitary corticogeniculate excitatory postsynaptic currents (EPSCs), whole cell patch-clamp recordings were obtained from 20 principal cells in slices of the dorsal lateral geniculate nucleus (dLGN) of DA-HAN rats. EPSCs, evoked by electrical stimulation of corticogeniculate axons, had size distributions with one or more quantal peaks. Gaussian curves fitted to such distributions gave a mean quantal size (q) of -5.0 +/- 0.7 (SD) pA for the EPSCs. Paired-pulse ratio (EPSC2/EPSC1) was 3.3 +/- 0.9 for stimuli separated by 40 ms. The mean quantal size was similar for facilitated EPSCs (-5.2 +/- 0.8 pA), implying an increase in mean quantal content (m). Most corticogeniculate axons were capable of releasing only one or two quanta onto individual principal cells. Mean resting release probability (p) was low, 0.09 +/- 0.04. Binomial models, with the same n but increased p, could account for both the basal and facilitated EPSC size distributions in 6/8 cells. It is suggested that the low resting efficacy of corticogeniculate synapses serves to stabilize this excitatory feedback system. The pronounced facilitation in conjunction with large convergence from many corticogeniculate cells would provide a transient, potent excitation of dLGN cells, compliant with the idea of a visually driven neuronal amplifier.

[1]  J. Bourassa,et al.  Corticothalamic projections from the primary visual cortex in rats: a single fiber study using biocytin as an anterograde tracer , 1995, Neuroscience.

[2]  K. Grant,et al.  Monosynaptic excitation of principal cells in the lateral geniculate nucleus by corticofugal fibers , 1982, Brain Research.

[3]  D Ferster,et al.  Synaptic excitation of neurones in area 17 of the cat by intracortical axon collaterals of cortico‐geniculate cells. , 1985, The Journal of physiology.

[4]  D Ferster,et al.  Augmenting responses evoked in area 17 of the cat by intracortical axon collaterals of cortico‐geniculate cells. , 1985, The Journal of physiology.

[5]  Involvement of the eyes in sequestral inflammation of the dental germ in infants , 1954 .

[6]  G B Arden,et al.  The Visual System , 2021, AMA Guides to the Evaluation of Permanent Impairment, 6th Edition, 2021.

[7]  H. Atwood,et al.  Diversification of synaptic strength: presynaptic elements , 2002, Nature Reviews Neuroscience.

[8]  Björn Granseth,et al.  Paired pulse facilitation of corticogeniculate EPSCs in the dorsal lateral geniculate nucleus of the rat investigated in vitro , 2002, The Journal of physiology.

[9]  T. Salt,et al.  Characterization of sensory and corticothalamic excitatory inputs to rat thalamocortical neurones in vitro , 1998, The Journal of physiology.

[10]  B. Walmsley,et al.  Counting quanta: Direct measurements of transmitter release at a central synapse , 1995, Neuron.

[11]  S. Sherman,et al.  Relative numbers of cortical and brainstem inputs to the lateral geniculate nucleus. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[12]  B. Sakmann,et al.  Quantal components of unitary EPSCs at the mossy fibre synapse on CA3 pyramidal cells of rat hippocampus. , 1993, The Journal of physiology.

[13]  George L. Gerstein,et al.  Feature-linked synchronization of thalamic relay cell firing induced by feedback from the visual cortex , 1994, Nature.

[14]  G. Paxinos The Rat nervous system , 1985 .

[15]  J. Deuchars,et al.  Properties of single axon excitatory postsynaptic potentials elicited in spiny interneurons by action potentials in pyramidal neurons in slices of rat neocortex , 1995, Neuroscience.

[16]  S. Lindström,et al.  Frequency dependent corticofugal excitation of principal cells in the cat's dorsal lateral geniculate nucleus , 2004, Experimental Brain Research.

[17]  B Sakmann,et al.  Quantal analysis of inhibitory synaptic transmission in the dentate gyrus of rat hippocampal slices: a patch‐clamp study. , 1990, The Journal of physiology.

[18]  G. Ahlsén,et al.  Interaction between inhibitory pathways to principal cells in the lateral geniculate nucleus of the cat , 2004, Experimental Brain Research.

[19]  C. Stevens,et al.  Facilitation and depression at single central synapses , 1995, Neuron.

[20]  M. Bennett,et al.  Statistics of transmitter release at nerve terminals , 2000, Progress in Neurobiology.

[21]  K. Martin,et al.  Intracortical excitation of spiny neurons in layer 4 of cat striate cortex in vitro. , 1999, Cerebral cortex.

[22]  B. Katz,et al.  Quantal components of the end‐plate potential , 1954, The Journal of physiology.

[23]  J. Parnavelas,et al.  The postnatal development of neurons in the dorsal lateral geniculate nucleus of the rat: A Golgi study , 1977, The Journal of comparative neurology.

[24]  D. McCormick,et al.  Corticothalamic activation modulates thalamic firing through glutamate "metabotropic" receptors. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[25]  W. Regehr,et al.  Determinants of the Time Course of Facilitation at the Granule Cell to Purkinje Cell Synapse , 1996, The Journal of Neuroscience.

[26]  C. Gilbert,et al.  The projections of cells in different layers of the cat's visual cortex , 1975, The Journal of comparative neurology.

[27]  C. Stevens,et al.  Heterogeneity of Release Probability, Facilitation, and Depletion at Central Synapses , 1997, Neuron.

[28]  R. Guillery,et al.  Thalamic Relay Functions and Their Role in Corticocortical Communication Generalizations from the Visual System , 2002, Neuron.

[29]  D. Ferster,et al.  An intracellular analysis of geniculo‐cortical connectivity in area 17 of the cat. , 1983, The Journal of physiology.

[30]  D. McCormick,et al.  Dynamic properties of corticothalamic excitatory postsynaptic potentials and thalamic reticular inhibitory postsynaptic potentials in thalamocortical neurons of the guinea-pig dorsal lateral geniculate nucleus , 1999, Neuroscience.

[31]  K. Magleby,et al.  Is the quantum of transmitter release composed of subunits? A critical analysis in the mouse and frog , 1981, Nature.

[32]  P. C. Murphy,et al.  Functional morphology of the feedback pathway from area 17 of the cat visual cortex to the lateral geniculate nucleus , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[33]  P Heggelund,et al.  Quantal properties of spontaneous EPSCs in neurones of the guinea‐pig dorsal lateral geniculate nucleus. , 1996, The Journal of physiology.

[34]  D. Hubel,et al.  Integrative action in the cat's lateral geniculate body , 1961, The Journal of physiology.

[35]  R. W. Güillery A quantitative study of synaptic interconnections in the dorsal lateral geniculate nucleus of the cat , 2004, Zeitschrift für Zellforschung und Mikroskopische Anatomie.

[36]  P Heggelund,et al.  The quantal size at retinogeniculate synapses determined from spontaneous and evoked EPSCs in guinea‐pig thalamic slices. , 1994, The Journal of physiology.

[37]  B. Katz,et al.  Statistical factors involved in neuromuscular facilitation and depression , 1954, The Journal of physiology.

[38]  Reid R. Clay,et al.  Specificity and strength of retinogeniculate connections. , 1999, Journal of neurophysiology.

[39]  M. Bennett,et al.  The effect of calcium ions and temperature on the binomial parameters that control acetylcholine release by a nerve impulse at amphibian neuromuscular synapses , 1977, The Journal of physiology.

[40]  P. Andersen,et al.  Putative Single Quantum and Single Fibre Excitatory Postsynaptic Currents Show Similar Amplitude Range and Variability in Rat Hippocampal Slices , 1992, The European journal of neuroscience.

[41]  E. G. Jones,et al.  Differences in quantal amplitude reflect GluR4- subunit number at corticothalamic synapses on two populations of thalamic neurons , 2001, Proceedings of the National Academy of Sciences of the United States of America.