Suppression at high spatial frequencies in the lateral geniculate nucleus of the cat.

The spatial weighting functions of both retinal and lateral geniculate nucleus (LGN) X-cell receptive fields have been viewed as the difference of two Gaussians (DOG). We focus on a particular shortcoming of the DOG model, that is, suppression of responses of LGN cells at spatial frequencies above those to which the classical receptive field surround is responsive. By simultaneously recording one of the retinal ganglion cell (RGC) inputs (S-potentials) to an LGN cell, we find that half of this suppression at high spatial frequencies arises from the retinal input and that suppression in LGN cells is greater than that in RGCs, regardless of spatial frequency. We also inactivated the ipsilateral visual cortex and show that one quarter of the suppression at high spatial frequencies arises from corticothalamic feedback. We show that this suppression at high spatial frequencies is colocalized with the classical surround, is not dependent on the relative orientation of the center and surround stimuli, and that the cortical component of this suppression is divisive. We propose that the role of this suppression at high spatial frequencies is to restrict the response to large stimuli composed of high spatial frequencies.

Contrast-dependent spatial summation in the lateral geniculate nucleus and retina of the cat.

Based on extracellular recordings from 69 lateral geniculate nucleus (LGN) cells in the anesthetized cat, we found spatial summation within their receptive fields to be dependent on the contrast of the stimuli presented. By fitting the summation curves to a difference of Gaussians model, we attributed this contrast-dependent effect to an actual change in the size of the center mechanism. Analogous changes in spatial frequency tuning were also observed, specifically increased peaks and cut-off frequencies with contrast. These effects were seen across the populations of both X and Y cell types. In a few cases, LGN cells were recorded simultaneously with one of their retinal ganglion cell (RGC) inputs (S-potentials). In every case, the RGCs exhibited similar contrast-dependent effects in the space and spatial-frequency domains. We propose that this contrast dependency in the retinal ganglion cells results directly from a reduction in the size of the center mechanism due to an increase in contrast. We also propose that these properties first arise in the retina and are transmitted passively through the LGN to visual cortex.