학술논문

Neuronal response properties across cytochrome oxidase stripes in primate V2.
Document Type
Article
Source
Journal of Comparative Neurology. Feb2019, Vol. 527 Issue 3, p651-667. 17p.
Subject
Language
ISSN
0021-9967
Abstract
Cytochrome oxidase histochemistry reveals large‐scale cortical modules in area V2 of primates known as thick, thin, and interstripes. Anatomical, electrophysiological, and tracing studies suggest that V2 cytochrome oxidase stripes participate in functionally distinct streams of visual information processing. However, there is controversy whether the different V2 compartments indeed correlate with specialized neuronal response properties. We used multiple‐electrode arrays (16 × 2, 8 × 4 and 4 × 4 matrices) to simultaneously record the spiking activity (N = 190 single units) across distinct V2 stripes in anesthetized and paralyzed capuchin monkeys (N = 3 animals, 6 hemispheres). Visual stimulation consisted of moving bars and full‐field gratings with different contrasts, orientations, directions of motion, spatial frequencies, velocities, and color contrasts. Interstripe neurons exhibited the strongest orientation and direction selectivities compared to the thick and thin stripes, with relatively stronger coding for orientation. Additionally, they responded best to higher spatial frequencies and to lower stimulus velocities. Thin stripes showed the highest proportion (80%) of neurons selective to color contrast (compared to 47% and 21% for thick and interstripes, respectively). The great majority of the color selective cells (86%) were also orientation selective. Additionally, thin stripe neurons continued to increase their firing rate for stimulus contrasts above 50%, while thick and interstripe neurons already exhibited some degree of response saturation at this point. Thick stripes best coded for lower spatial frequencies and higher stimulus velocities. In conclusion, V2 CytOx stripes exhibit a mixed degree of segregation and integration of information processing, shedding light into the early mechanisms of vision. Histochemical processing for the CytOx enzyme was used to assign each electrode of the array to a specific V2 stripe or module. The 16‐by‐2 electrode array was positioned so that its long axis was oriented parallel to the V1–V2 border in order to maximize sampling across the 3 types of V2 stripes. In this case, we simultaneously sample from up to 2 full sets of V2 stripes. [ABSTRACT FROM AUTHOR]