scholarly journals Stimulus Contrast Affects Spatial Integration in the Lateral Geniculate Nucleus of Macaque Monkeys

2021 ◽  
pp. JN-RM-2946-20
Author(s):  
Darlene R. Archer ◽  
Henry J. Alitto ◽  
W. Martin Usrey
2000 ◽  
Vol 20 (16) ◽  
pp. 6030-6038 ◽  
Author(s):  
Noriyuki Higo ◽  
Takao Oishi ◽  
Akiko Yamashita ◽  
Keiji Matsuda ◽  
Motoharu Hayashi

2004 ◽  
Vol 91 (1) ◽  
pp. 438-448 ◽  
Author(s):  
Sabine Kastner ◽  
Daniel H. O'Connor ◽  
Miki M. Fukui ◽  
Hilda M. Fehd ◽  
Uwe Herwig ◽  
...  

In the human brain, little is known about the functional anatomy and response properties of subcortical nuclei containing visual maps such as the lateral geniculate nucleus (LGN) and the pulvinar. Using functional magnetic resonance imaging (fMRI) at 3 tesla (T), collective responses of neural populations in the LGN were measured as a function of stimulus contrast and flicker reversal rate and compared with those obtained in visual cortex. Flickering checkerboard stimuli presented in alternation to the right and left hemifields reliably activated the LGN. The peak of the LGN activation was found to be on average within ±2 mm of the anatomical location of the LGN, as identified on high-resolution structural images. In all visual areas except the middle temporal (MT), fMRI responses increased monotonically with stimulus contrast. In the LGN, the dynamic response range of the contrast function was larger and contrast gain was lower than in the cortex. Contrast sensitivity was lowest in the LGN and V1 and increased gradually in extrastriate cortex. In area MT, responses were saturated at 4% contrast. Response modulation by changes in flicker rate was similar in the LGN and V1 and occurred mainly in the frequency range between 0.5 and 7.5 Hz; in contrast, in extrastriate areas V4, V3A, and MT, responses were modulated mainly in the frequency range between 7.5 and 20 Hz. In the human pulvinar, no activations were obtained with the experimental designs used to probe response properties of the LGN. However, regions in the mediodorsal right and left pulvinar were found to be consistently activated by bilaterally presented flickering checkerboard stimuli, when subjects attended to the stimuli. Taken together, our results demonstrate that fMRI at 3 T can be used effectively to study thalamocortical circuits in the human brain.


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.


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