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Alex R Wade

Publications and source records attributed to Alex R Wade.

5 recordsLinked to original sources

Functional imaging of the visual pathways.

Functional neuroimaging has provided a new view of activity in human visual cortex. There have been a series of interesting developments in understanding the relationship between the functional signals, particularly functional MRI, and basic measurements of action potentials and local field potentials. The new human neuro-imaging measurements have clarified some of the similarities and differences between the general organization of visual areas in human and macaque visual cortex, and there have been some interesting new results concerning cortical visual plasticity and dysfunction. The new fMRI focus on measurements of the human brain will drive new relationships between neurology and visual neuroscience that should help us learn much more about the neural basis of perception.

Electroencephalography↗

The negative BOLD signal unmasked.

Many fMRI experiments show regions of cortex that seem to respond in antiphase with the primary stimulus. In this issue of Neuron, Shmuel et al. show that this "negative BOLD response" is spatially and temporally linked to reductions in blood flow. By combining BOLD and blood flow data to model the energy consumption in cortex, they conclude that the NBR is primarily due to active neuronal inhibition.

Cerebral Cortex↗

Chromatic light adaptation measured using functional magnetic resonance imaging.

Sensitivity changes, beginning at the first stages of visual transduction, permit neurons with modest dynamic range to respond to contrast variations across an enormous range of mean illumination. We have used functional magnetic resonance imaging (fMRI) to investigate how these sensitivity changes are controlled within the visual pathways. We measured responses in human visual area V1 to a constant-amplitude, contrast-reversing probe presented on a range of mean backgrounds. We found that signals from probes initiated in the L and M cones were affected by backgrounds that changed the mean absorption rates in the L and M cones, but not by background changes seen only by the S cones. Similarly, signals from S cone-initiated probes were altered by background changes in the S cones, but not by background changes in the L and M cones. Performance in psychophysical tests under similar conditions closely mirrored the changes in V1 fMRI signals. We compare our data with simulations of the visual pathway from photon catch rates to cortical blood-oxygen level-dependent signals and show that the quantitative fMRI signals are consistent with a simple model of mean-field adaptation based on Naka-Rushton (Naka and Rushton, 1966) adaptation mechanisms within cone photoreceptor classes.

Adaptation, Ocular↗

Functional measurements of human ventral occipital cortex: retinotopy and colour.

Human colour vision originates in the cone photoreceptors, whose spatial density peaks in the fovea and declines rapidly into the periphery. For this reason, one expects to find a large representation of the cone-rich fovea in those cortical locations that support colour perception. Human occipital cortex contains several distinct foveal representations including at least two that extend onto the ventral surface: a region thought to be critical for colour vision. To learn more about these ventral signals, we used functional magnetic resonance imaging to identify visual field maps and colour responsivity on the ventral surface. We found a visual map of the complete contralateral hemifield in a 4 cm(2) region adjacent to ventral V3; the foveal representation of this map is confluent with that of areas V1/2/3. Additionally, a distinct foveal representation is present on the ventral surface situated 3-5 cm anterior from the confluent V1/2/3 foveal representations. This organization is not consistent with the definition of area V8, which assumes the presence of a quarter field representation adjacent to V3v. Comparisons of responses to luminance-matched coloured and achromatic patterns show increased activity to the coloured stimuli beginning in area V1 and extending through the new hemifield representation and further anterior in the ventral occipital lobe.

Brain Mapping↗