Effects of LSD on Receptive Fields of Single Cells in the Lateral Geniculate Nucleus of the Cat

Nature ◽  
1971 ◽  
Vol 229 (5283) ◽  
pp. 347-349 ◽  
Author(s):  
JENNIFER M. MCKAY ◽  
GABRIEL HORN
Keyword(s):  
Lateral Geniculate Nucleus ◽  
Single Cells ◽  
Receptive Fields ◽  
Lateral Geniculate

Response properties of cells in rabbit's lateral geniculate nucleus during reversible blockade of retinal on-center channel

1983 ◽  
Vol 50 (5) ◽  
pp. 1236-1245 ◽  
Author(s):  
A. G. Knapp ◽  
L. A. Mistler
Keyword(s):  
Lateral Geniculate Nucleus ◽  
Visual Information ◽  
Single Cells ◽  
Receptive Fields ◽  
Uniform Field ◽  
Vertebrate Species ◽  
Response Properties ◽  
Lateral Geniculate ◽  
Functional Classes ◽  
On And Off Pathways

In the vertebrate retina, visual information is segregated into an on channel excited by light increment and a complementary off channel excited by light decrement. We used 2-amino-4-phosphonobutyric acid (APB), which selectively blocks the on channel in the retina (29), to determine the contributions of the on and off pathways to response properties of neurons in the lateral geniculate nucleus (LGN) of anesthetized, paralyzed rabbits. Visually evoked responses were recorded from 46 single cells in the LGN before, during, and after vitreal perfusion with 200-1,000 microM APB. APB reversibly blocked responses of on uniform-field cells and on center concentric-field cells to stationary, flashing spots of light. Responses to off uniform-field cells and off-center concentric-field cells were largely unaffected. APB did not differentially affect responses elicited from the receptive-field centers, as opposed to the surrounds, of on-center concentric-field cells. This finding suggests that these cells are driven exclusively by the on retinal channel and that the center-surround organization of their receptive fields does not result from a convergence of the on and off pathways. We studied a small number of cells that were selective for stimulus direction or motion. In each case, APB eliminated the cell's response to a moving light edge. The surviving response to a moving dark edge retained its original direction or motion preference, suggesting that these response properties do not depend critically on interactions between the on and the off pathways. The findings obtained in the rabbit are reminiscent of the results of similar investigations in the cat (10, 11) and the monkey (25). Taken together, they indicate that in the LGN of several vertebrate species there is a precise segregation vertebrate species there is a precise segregation of on and off information, at least for some functional classes of cells. The combination of on and off information does not seem to play a major role in establishing the response properties observed at this level in the visual system.

Spatial limits of epileptogenic cortex: its relationship to ectopic spike generation

1975 ◽  
Vol 38 (2) ◽  
pp. 395-404 ◽  
Author(s):  
A. J. Gabor ◽  
R. P. Scobey
Keyword(s):  
Lateral Geniculate Nucleus ◽  
Direct Effect ◽  
Receptive Fields ◽  
Spike Generation ◽  
Lateral Geniculate

In order to investigate if ectopic spike generation was ubiquitous in and specific generation was ubiquitous in and specific to epileptogenic cortex, a method was devised to determine the limits of such an area based on a well-accepted physiologic characteristic of epileptogenicity. The limits of the penicillin-induced epileptogenic cortex were defined in terms of a retinal activation field; this is a circumscribed area whose stimulation by light evokes a characteristic cortical epileptiform wave. All lateral geniculate nucleus (LGN) neurons manifesting ectopic spike generation during interictal epileptiform waves had receptive fields within the activation field. During organized seizures, ectopic spike generation was observed in neurons with receptive fields outside the activation field. Because of these findings it was concluded that ectopic spike generation is a characteristic and specific feature of epileptogenic cortex and that it is a characteristic of the epeleptogenic process rather than a peripheral event related entirely to the direct effect of penicillin on neurons.

Mathematical models for the spatial receptive-field organization of nonlagged X-cells in dorsal lateral geniculate nucleus of cat

2000 ◽  
Vol 17 (6) ◽  
pp. 871-885 ◽  
Author(s):  
G.T. EINEVOLL ◽  
P. HEGGELUND
Keyword(s):  
Receptive Field ◽  
Ganglion Cell ◽  
Lateral Geniculate Nucleus ◽  
Discrete Model ◽  
Receptive Fields ◽  
Dorsal Lateral Geniculate Nucleus ◽  
Retinal Ganglion ◽  
Lateral Geniculate ◽  
X Cells ◽  
Dorsal Lateral Geniculate

Spatial receptive fields of relay cells in dorsal lateral geniculate nucleus (dLGN) have commonly been modeled as a difference of two Gaussian functions. We present alternative models for dLGN cells which take known physiological couplings between retina and dLGN and within dLGN into account. The models include excitatory input from a single retinal ganglion cell and feedforward inhibition via intrageniculate interneurons. Mathematical formulas describing the receptive field and response to circular spot stimuli are found both for models with a finite and an infinite number of ganglion-cell inputs to dLGN neurons. The advantage of these models compared to the common difference-of-Gaussians model is that they, in addition to providing mathematical descriptions of the receptive fields of dLGN neurons, also make explicit contributions from the geniculate circuit. Moreover, the model parameters have direct physiological relevance and can be manipulated and measured experimentally. The discrete model is applied to recently published data (Ruksenas et al., 2000) on response versus spot-diameter curves for dLGN cells and for the retinal input to the cell (S-potentials). The models are found to account well for the results for the X-cells in these experiments. Moreover, predictions from the discrete model regarding receptive-field sizes of interneurons, the amount of center-surround antagonism for interneurons compared to relay cells, and distance between neighboring retinal ganglion cells providing input to interneurons, are all compatible with data available in the literature.

scholarly journals Spatial receptive fields in the retina and dorsal lateral geniculate nucleus of mice lacking rods and cones

2015 ◽  
Vol 114 (2) ◽  
pp. 1321-1330 ◽  
Author(s):  
Christopher A. Procyk ◽  
Cyril G. Eleftheriou ◽  
Riccardo Storchi ◽  
Annette E. Allen ◽  
Nina Milosavljevic ◽  
...  
Keyword(s):  
Retinal Degeneration ◽  
Lateral Geniculate Nucleus ◽  
Visual Information ◽  
Spatial Information ◽  
Receptive Fields ◽  
Dorsal Lateral Geniculate Nucleus ◽  
Multielectrode Arrays ◽  
Rods And Cones ◽  
Lateral Geniculate ◽  
Dorsal Lateral Geniculate

In advanced retinal degeneration loss of rods and cones leaves melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs) as the only source of visual information. ipRGCs drive non-image-forming responses (e.g., circadian photoentrainment) under such conditions but, despite projecting to the primary visual thalamus [dorsal lateral geniculate nucleus (dLGN)], do not support form vision. We wished to determine what precludes ipRGCs supporting spatial discrimination after photoreceptor loss, using a mouse model ( rd/rd cl) lacking rods and cones. Using multielectrode arrays, we found that both RGCs and neurons in the dLGN of this animal have clearly delineated spatial receptive fields. In the retina, they are typically symmetrical, lack inhibitory surrounds, and have diameters in the range of 10–30° of visual space. Receptive fields in the dLGN were larger (diameters typically 30–70°) but matched the retinotopic map of the mouse dLGN. Injections of a neuroanatomical tracer (cholera toxin β-subunit) into the dLGN confirmed that retinotopic order of ganglion cell projections to the dLGN and thalamic projections to the cortex is at least superficially intact in rd/rd cl mice. However, as previously reported for deafferented ipRGCs, onset and offset of light responses have long latencies in the rd/rd cl retina and dLGN. Accordingly, dLGN neurons failed to track dynamic changes in light intensity in this animal. Our data reveal that ipRGCs can convey spatial information in advanced retinal degeneration and identify their poor temporal fidelity as the major limitation in their ability to provide information about spatial patterns under natural viewing conditions.

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