Transfer characteristics of lateral geniculate nucleus X neurons in the cat: effects of spatial frequency and contrast

1995 ◽  
Vol 74 (6) ◽  
pp. 2548-2557 ◽  
Author(s):  
H. Cheng ◽  
Y. M. Chino ◽  
E. L. Smith ◽  
J. Hamamoto ◽  
K. Yoshida

1. The dependence of signal transfer in the lateral geniculate nucleus (LGN) on stimulus spatial frequency and contrast was investigated by comparing responses of individual X cells with their direct retinal inputs. 2. We used extracellular single-cell recording methods to isolate action potentials (LGN) and S potentials (SPs) from individual neurons in layers A and A1 of anesthetized and paralyzed cats. The stimuli were drifting sinusoidal gratings that were presented at each neuron's preferred orientation. The effects of stimulus spatial frequency and contrast on retinogeniculate signal transfer were determined by comparing the amplitude of the fundamental Fourier responses measured for a cell's action potentials (LGN) and its retinal input (SP) and calculating the transfer ratio (LGN amplitude/SP amplitude) for each stimulus condition. 3. In all units, the LGN response amplitude was lower than that of its retinal input regardless of stimulus spatial frequency. The mean transfer ratio measured at the peak spatial frequency for individual units was 0.56 +/- 0.03 (SE). For the majority of X LGN neurons, however, the efficiency of signal transfer varied considerably with stimulus spatial frequency. The average transfer ratio increased monotonically from 0.08 cycle/deg to near the high cutoff spatial frequency. 4. The effects of stimulus contrast on geniculate signal transfer were far more complex than previously reported and varied substantially between individual neurons. At low stimulus contrasts (< 10%), where all units exhibited linear response characteristics, only one third of our sample showed a monotonic decrease in transfer ratio with increasing stimulus contrast. The remaining two thirds either exhibited proportionately greater signal transfer for higher stimulus contrasts, or signal transfer remained relatively unchanged with increasing stimulus contrasts. When stimulus contrasts exceeded 10%, where response amplitude began to saturate, the transfer ratio was relatively constant in all units and independent of stimulus contrast. 5. Our results demonstrate that signal transfer from retina to visual cortex is regulated by LGN neurons in a stimulus-dependent manner, which appears to reflect the complex interactions between local membrane mechanisms and extraretinal inputs.

2009 ◽  
Vol 65 ◽  
pp. S106
Author(s):  
Akihiro Kimura ◽  
Satoshi Shimegi ◽  
Shin-ichiro Hara ◽  
Masahiro Okamoto ◽  
Hiromichi Sato

1984 ◽  
Vol 52 (5) ◽  
pp. 911-920 ◽  
Author(s):  
J. Frascella ◽  
S. Lehmkuhle

Extracellular responses of Y-cells in the A-laminae and in lamina C of the cat dorsal lateral geniculate nucleus were recorded and compared for several sine-wave grating presentations. Both spatial and temporal contrast sensitivity functions were determined for these cells as well as suprathreshold response functions at 0.2 and 0.4 contrast. Qualitatively, the responses of the lamina C Y-cells were very similar to Y-cells of the A-laminae; differences were of a quantitative nature. At threshold, lamina C Y-cells were more sensitive at all spatial and temporal frequencies tested. Suprathreshold results showed no major differences in fundamental response amplitude between laminar Y-cells. Interlaminar differences were found with respect to second harmonic response amplitude. Lamina C Y-cells gave the largest overall second harmonic response for all stimulus conditions. A trend was observed for these laminar Y-cells such that the second harmonic responses were highest for Y-cells of lamina C, intermediate for lamina A Y-cells, and lowest for those of lamina A1. Based on differences in projection pattern and present electrophysiological results, we conclude that the lamina C Y-cells may represent a population of cells that is distinct from A-laminae Y-cells. These lamina C Y-cells provide a significant input to visual cortex.


2008 ◽  
Vol 25 (1) ◽  
pp. 39-51 ◽  
Author(s):  
GESCHE BORN ◽  
MATTHIAS SCHMIDT

The ventral lateral geniculate nucleus (vLGN), the pretectal nuclear complex (PNC) and the superior colliculus (SC) are structures that all receive retinal input. All three structures are important relay stations of the subcortical visual system. They are strongly connected with each other and involved in circadian and/or visuomotor processes. However, the information transferred along these pathways is unknown and their possible functions are, therefore, not well understood. Here, we characterized multiple pathways between the vLGN, the PNC, and the SC electrophysiologically and anatomically in anin vitrostudy using acute rat brain slices. Using orthodromic and antidromic electrical stimulation, we first characterized vLGN neurons that receive pretectal input and those that project to the PNC. Morphological reconstructions of cells labeled after patch clamp recordings identified these neurons as geniculo-tectal neurons and as medium-sized multipolar neurons. We identified inhibitory connections in both pathways and we could show that inhibitory postsynaptic currents (IPSCs) evoked from the PNC in vLGN neurons are mediated only by GABAAreceptors, while IPSCs evoked in PNC neurons by vLGN stimulation are either mediated by both, GABAAand GABACreceptors or by a GABA receptor with mixed GABAAand GABACreceptor-like pharmacology. Finally, retrograde double labeling experiments with two different fluorescent dextran amines indicated that pretectal neurons which project to the ipsilateral vLGN also project to the ipsilateral SC.


1999 ◽  
Vol 81 (2) ◽  
pp. 702-711 ◽  
Author(s):  
J. Julius Zhu ◽  
William W. Lytton ◽  
Jin-Tang Xue ◽  
Daniel J. Uhlrich

Intrinsic oscillation in interneurons of the rat lateral geniculate nucleus. By using the whole cell patch recording technique in vitro, we examined the voltage-dependent firing patterns of 69 interneurons in the rat dorsal lateral geniculate nucleus (LGN). When held at a hyperpolarized membrane potential, all interneurons responded with a burst of action potentials. In 48 interneurons, larger current pulses produced a bursting oscillation. When relatively depolarized, some interneurons produced a tonic train of action potentials in response to a depolarizing current pulse. However, most interneurons produced only oscillations, regardless of polarization level. The oscillation was insensitive to the bath application of a combination of blockers to excitatory and inhibitory synaptic transmission, including 30 μM 6,7-dinitroquinoxaline-2,3-dione, 100 μM (±)-2-amino-5-phosphonopentanoic acid, 20 μM bicuculline, and 2 mM saclofen, suggesting an intrinsic event. The frequency of the oscillation in interneurons was dependent on the intensity of the injection current. Increasing current intensity increased the oscillation frequency. The maximal frequency of the oscillation was 5–15 Hz for most cells, with some ambiguity caused by the difficulty of precisely defining a transition from oscillatory to regular firing behavior. In contrast, the interneuron oscillation was little affected by preceding depolarizing and hyperpolarizing pulses. In addition to being elicited by depolarizing current injections, the oscillation could also be initiated by electrical stimulation of the optic tract when the interneurons were held at a depolarized membrane potential. This suggests that interneurons may be recruited into thalamic oscillations by synaptic inputs. These results indicate that interneurons may play a larger role in thalamic oscillations than was previously thought.


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