Dc. Kadunce et al., MECHANISMS OF WITHIN-MODALITY AND CROSS-MODALITY SUPPRESSION IN THE SUPERIOR COLLICULUS, Journal of neurophysiology, 78(6), 1997, pp. 2834-2847
The present studies were initiated to explore the basis for the respon
se suppression that occurs in cat superior colliculus (SC) neurons whe
n two spatially disparate stimuli are presented simultaneously or in c
lose temporal proximity to one another. Of specific interest was exami
ning the possibility that suppressive regions border the receptive fie
lds (RFs) of unimodal and multisensory SC neurons and, when activated,
degrade the neuron's responses to excitatory stimuli. Both within-and
cross-modality effects were examined. An example of the former is whe
n a response to a visual stimulus within its RF is suppressed by a sec
ond visual stimulus outside the RF. An example of the latter is when t
he response to a visual stimulus within the visual RF is suppressed wh
en a stimulus from a different modality (e.g., auditory) is presented
outside its (i.e., auditory) RF. Suppressive regions were found border
ing visual, auditory, and somatosensory RFs. Despite significant modal
ity-specific differences in the incidence and effectiveness of these r
egions, they were generally quite potent regardless of the modality. I
n the vast majority (85%) of cases, responses to the excitatory stimul
us were degraded by greater than or equal to 50% by simultaneously sti
mulating the suppressive region. Contrary to expectations and previous
speculations, the effects of activating these suppressive regions oft
en were quite specific. Thus powerful within-modality suppression coul
d be demonstrated in many multisensory neurons in which cross-modality
suppression could not be generated. However, the converse was not tru
e. If an extra-RF stimulus inhibited center responses to stimuli of a
different modality, it also would suppress center responses to stimuli
of its own modality. Thus when cross-modality suppression was demonst
rated, it was always accompanied by within-modality suppression. These
observations suggest that separate mechanisms underlie within-and cro
ss-modality suppression in the SC. Because some modality-specific tect
opetal structures contain neurons with suppressive regions bordering t
heir RFs, the within-modality suppression observed in the SC simply ma
y reflect interactions taking place at the level of one input channel.
However, the presence of modality-specific suppression at the level o
f one input channel would have no effect on the excitation initiated v
ia another input channel. Given the modality-specificity of tectopetal
inputs, it appears that cross-modality interactions require the conve
rgence of two or more modality-specific inputs onto the same SC neuron
and that the expression of these interactions depends on the internal
circuitry of the SC. This allows a cross-modality suppressive signal
to be nonspecific and to degrade any and all of the neuron's excitator
y inputs.