Binocular disparity tuning and visual-vestibular congruency of multisensory neurons in macaque parietal cortex.

Many neurons in the dorsal medial superior temporal (MSTd) and ventral intraparietal (VIP) areas of the macaque brain are multisensory, responding to both optic flow and vestibular cues to self-motion. The heading tuning of visual and vestibular responses can be either congruent or opposite, but only congruent cells have been implicated in cue integration for heading perception. Because of the geometric properties of motion parallax, however, both congruent and opposite cells could be involved in coding self-motion when observers fixate a world-fixed target during translation, if congruent cells prefer near disparities and opposite cells prefer far disparities.

Coding of stereoscopic depth information in visual areas V3 and V3A.

The process of stereoscopic depth perception is thought to begin with the analysis of absolute binocular disparity, the difference in position of corresponding features in the left and right eye images with respect to the points of fixation. Our sensitivity to depth, however, is greater when depth judgments are based on relative disparity, the difference between two absolute disparities, compared to when they are based on absolute disparity. Therefore, the visual system is thought to compute relative disparities for fine depth discrimination.

Does the middle temporal area carry vestibular signals related to self-motion?

Recent studies have described vestibular responses in the dorsal medial superior temporal area (MSTd), a region of extrastriate visual cortex thought to be involved in self-motion perception. The pathways by which vestibular signals are conveyed to area MSTd are currently unclear, and one possibility is that vestibular signals are already present in areas that are known to provide visual inputs to MSTd. Thus, we examined whether selective vestibular responses are exhibited by single neurons in the middle temporal area (MT), a visual motion-sensitive region that projects heavily to area MSTd.

Fine discrimination training alters the causal contribution of macaque area MT to depth perception.

When a new perceptual task is learned, plasticity occurs in the brain to mediate improvements in performance with training. How do these changes affect the neural substrates of previously learned tasks? We addressed this question by examining the effect of fine discrimination training on the causal contribution of area MT to coarse depth discrimination. When monkeys are trained to discriminate between two coarse absolute disparities (near versus far) embedded in noise, reversible inactivation of area MT devastates performance.

Effect of vertical disparities on depth representation in macaque monkeys: MT physiology and behavior.

Horizontal binocular disparities provide information about the distance of objects relative to the point of ocular fixation and must be combined with an estimate of viewing distance to recover the egocentric distance of an object. Vergence angle and the gradient of vertical disparities across the visual field are thought to provide independent sources of viewing distance information based on human behavioral studies. Although the effect of vergence angle on horizontal disparity selectivity in early visual cortex has been examined (with mixed results), the effect of the vertical disparity field has not been explored.

GABA-B-related activity in processing of transcallosal response in cat motor cortex.

GABA-ergic characteristics of transcallosal (TC) responses were studied with specific antagonists of both GABA-A and GABA-B receptor subtypes. We used a paired-pulse paradigm to get insight into the role of GABA in interhemispheric interactions between motor cortices. 3-Amino-2-(4-chlorophenyl)-propylphosphonic acid (phaclofen) and 3-aminopropyl-diethoxymethyl-phosphinic acid (CGP 35348) were used as GABA-B antagonists and bicuculline methiodide (BMI) was used to block the GABA-A receptor.