scholarly journals Visual Motion Responses of Neurons in the Caudal Area PE of Macaque Monkeys

2001 ◽  
Vol 21 (4) ◽  
pp. RC130-RC130 ◽  
Author(s):  
Salvatore Squatrito ◽  
Milena Raffi ◽  
Maria Grazia Maioli ◽  
Alexandra Battaglia-Mayer
1992 ◽  
Vol 25 (5) ◽  
pp. 345-354 ◽  
Author(s):  
Akichika Mikami ◽  
Kazuo Fujita

2021 ◽  
Author(s):  
Fatemeh Molaei Vaneghi ◽  
Natalia Zaretskaya ◽  
Tim van Mourik ◽  
Jonas Bause ◽  
Klaus Scheffler ◽  
...  

Neural mechanisms underlying a stable perception of the world during pursuit eye movements are not fully understood. Both, perceptual stability as well as perception of real (i.e. objective) motion are the product of integration between motion signals on the retina and efference copies of eye movements. Human areas V3A and V6 have previously been shown to have strong objective ('real') motion responses. Here we used high-resolution laminar fMRI at ultra-high magnetic field (9.4T) in human subjects to examine motion integration across cortical depths in these areas. We found an increased preference for objective motion in areas V3A and V6+ i.e. V6 and possibly V6A towards the upper layers. When laminar responses were detrended to remove the upper-layer bias present in all responses, we found a unique, condition-specific laminar profile in V6+, showing reduced mid-layer responses for retinal motion only. The results provide evidence for differential, motion-type dependent laminar processing in area V6+. Mechanistically, the mid-layer dip suggests a special contribution of retinal motion to integration, either in the form of a subtractive (inhibitory) mid-layer input, or in the form of feedback into extragranular or infragranular layers. The results show that differential laminar signals can be measured in high-level motion areas in human occipitoparietal cortex, opening the prospect of new mechanistic insights using non-invasive brain imaging.


2010 ◽  
Vol 103 (5) ◽  
pp. 2889-2899 ◽  
Author(s):  
Seiji Ono ◽  
Michael J. Mustari

Smooth pursuit (SP) eye movements are used to maintain the image of a moving object on or near the fovea. Visual motion signals aid in driving SP and are necessary for its adaptation. The sources of visual error signals that support SP adaptation are incompletely understood but could involve neurons in cortical and brain stem areas with direction selective visual motion responses. Here we focus on the pretectal nucleus of the optic tract (NOT), which encodes retinal error information during SP. The aim of this study was to characterize the role of the NOT in SP adaptation. SP adaptation is typically produced using a double step of velocity ramp (double-step paradigm), where target speed either increases or decreases 100 ms after the beginning of a trial. In our study, we delivered a brief (200 ms) train of microelectrical stimulation (ES) in the left NOT to introduce directional error signals at the point in time where a second target speed would appear in a double-step paradigm. The target was extinguished coincidentally with the onset of the ES train. Initial eye acceleration (1st 100 ms) showed significant increases after 100 trials, which included left NOT stimulation during ongoing pursuit in an ipsiversive (leftward) direction. In contrast, initial eye acceleration showed significant decreases after repeated left NOT stimulation during contraversive (rightward) SP. Control studies performed using the same periodicity of NOT stimulation as in the preceding text but without accompanying SP did not induce changes in eye acceleration. In contrast, ES of the NOT paired with active SP produced gradual changes in eye acceleration similar to that observed in double-step paradigm. Therefore our findings support the suggestion that the NOT is an important source of visual error information for guiding motor learning during horizontal SP.


2011 ◽  
Vol 22 (4) ◽  
pp. 865-876 ◽  
Author(s):  
Elvira Fischer ◽  
Heinrich H. Bülthoff ◽  
Nikos K. Logothetis ◽  
Andreas Bartels

2004 ◽  
Vol 21 (6) ◽  
pp. 851-859 ◽  
Author(s):  
LYNNE KIORPES ◽  
J. ANTHONY MOVSHON

The development of spatial vision is relatively well documented in human and nonhuman primates. However, little is known about the development of sensitivity to motion. We measured the development of sensitivity to direction of motion, and the relationship between motion and contrast sensitivity in macaque monkeys as a function of age. Monkeys (Macaca nemestrina, aged between 10 days and 3 years) discriminated direction of motion in random-dot kinematograms. The youngest monkeys showed directionally selective orienting and the ability to integrate motion signals at large dot displacements and fast speeds. With age, coherence sensitivity improved for all spatial and temporal dot displacements tested. The temporal interval between the dots was far less important than the spatial offset in determining the animals' performance at all but the youngest ages. Motion sensitivity improved well beyond the end of the first postnatal year, when mid-spatial-frequency contrast sensitivity reached asymptote, and continued for at least 3 years. Sensitivity to contrast at high spatial frequencies also continued to develop beyond the end of the first year. We conclude that the development of motion sensitivity depends on mechanisms beyond the low-level filters presumed to limit acuity and contrast sensitivity, and most likely reflects the function of extrastriate visual areas.


2021 ◽  
Author(s):  
Roberto Caminiti ◽  
Gabriel Girard ◽  
Alexandra Battaglia-Mayer ◽  
Elena Borra ◽  
Andrea Schito ◽  
...  

ABSTRACTIn macaque monkeys, dorsal intraparietal areas are involved in several daily visuo-motor actions. However, their border and sources of cortical afferents remain loosely defined. Through a retrograde tracer and MRI diffusion-based tractography study here we show a complex organization of the dorsal bank of the IPS, which can be subdivided into a rostral area PEip, projecting to the spinal cord, and a caudal area MIP lacking such projections. Both areas include a rostral and a caudal sector, emerging from their ipsilateral, gradient-like connectivity profiles. As tractography estimations, we used the cross-sectional volume of the white matter bundles connecting each area with other parietal and frontal regions, after selecting ROIs corresponding to the injection sites of retrograde tracers. A quantitative analysis between the proportions of cells projecting to all sectors of PEip and MIP along the continuum of the dorsal bank of the IPS and tractography revealed a significant correlation between the two data sets for most connections. Moreover, tractography revealed “false positive” but plausible streamlines awaiting histological validation.


2011 ◽  
Vol 28 (5) ◽  
pp. 419-431 ◽  
Author(s):  
ZULEY RIVERA-ALVIDREZ ◽  
ICHI LIN ◽  
CHARLES M. HIGGINS

AbstractMotion-sensitive neurons in the visual systems of many species, including humans, exhibit a depression of motion responses immediately after being exposed to rapidly moving images. This motion adaptation has been extensively studied in flies, but a neuronal mechanism that explains the most prominent component of adaptation, which occurs regardless of the direction of motion of the visual stimulus, has yet to be proposed. We identify a neuronal mechanism, namely frequency-dependent synaptic depression, which explains a number of the features of adaptation in mammalian motion-sensitive neurons and use it to model fly motion adaptation. While synaptic depression has been studied mainly in spiking cells, we use the same principles to develop a simple model for depression in a graded synapse. By incorporating this synaptic model into a neuronally based model for elementary motion detection, along with the implementation of a center-surround spatial band-pass filtering stage that mimics the interactions among a subset of visual neurons, we show that we can predict with remarkable success most of the qualitative features of adaptation observed in electrophysiological experiments. Our results support the idea that diverse species share common computational principles for processing visual motion and suggest that such principles could be neuronally implemented in very similar ways.


1990 ◽  
Vol 63 (1) ◽  
pp. 37-59 ◽  
Author(s):  
D. A. Suzuki ◽  
J. G. May ◽  
E. L. Keller ◽  
R. D. Yee

1. In this study we sought to characterize the visual motion processing that exists in the dorsolateral pontine nucleus (DLPN) and make a comparison with the reported visual responses of the middle temporal (MT) and medial superior temporal (MST) areas of the monkey cerebral cortex. The DLPN is implicated as a component of the visuomotor interface involved with the regulation of smooth-pursuit eye movements, because it is a major terminus for afferents from MT and MST and also the source of efferents to cerebellar regions involved with eye-movement control. 2. Some DLPN cells were preferentially responsive to discrete (spot and bar) visual stimuli, or to large-field, random-dot pattern motion, or to both discrete and large-field visual motion. The results suggest differential input from localized regions of MT and MST. 3. The visual-motion responses of DLPN neurons were direction selective for 86% of the discrete visual responses and 95% of the large-field responses. Direction tuning bandwidths (full-width at 50% maximum response amplitude) averaged 107 degrees and 120 degrees for discrete and large-field visual motion responses, respectively. For the two visual response types, the direction index averaged 0.95 and 1.02, indicating that responses to stimuli moving in preferred directions were, on average, 20 and 50 times greater than responses to discrete or large-field stimulus movement in the opposite directions, respectively. 4. Most of the DLPN visual responses to movements of discrete visual stimuli exhibited increases in amplitude up to preferred retinal image speeds between 20 and 80 degrees/s, with an average preferred speed of 39 degrees/s. At higher speeds, the response amplitude of most units decreased, although a few units exhibited a broad saturation in response amplitude that was maintained up to at least 150 degrees/s before the response decreased. Over the range of speeds up to the preferred speeds, the sensitivity of DLPN neurons to discrete stimulus-related, retinal-image speed averaged 3.0 spikes/s per deg/s. The responses to large-field visual motion were less sensitive to retinal image speed and exhibited an average sensitivity of 1.4 spikes/s per deg/s before the visual response saturated. 5. DLPN and MT were quantitatively comparable with respect to degree of direction selectivity, retinal image speed tuning, and distribution of preferred speeds. Many DLPN receptive fields contained the fovea and were larger than those of MT and more like MST receptive fields in size.(ABSTRACT TRUNCATED AT 400 WORDS)


NeuroImage ◽  
2015 ◽  
Vol 119 ◽  
pp. 187-196 ◽  
Author(s):  
Fang Jiang ◽  
Michael S. Beauchamp ◽  
Ione Fine

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