scholarly journals Visuotopic organization of bush baby primary visual cortex (V1) revealed by optical imaging

2010 ◽  
Vol 3 (9) ◽  
pp. 376-376 ◽  
Author(s):  
E. E Emeric ◽  
X Xu ◽  
J Mavity-Hudson ◽  
M Gallucci ◽  
A Thomas ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Optical Imaging ◽  
Primary Visual Cortex ◽  
Bush Baby

Differential contributions of magnocellular and parvocellular pathways to the contrast response of neurons in bush baby primary visual cortex (V1)

2000 ◽  
Vol 17 (1) ◽  
pp. 71-76 ◽  
Author(s):  
JOHN D. ALLISON ◽  
PETER MELZER ◽  
YUCHUAN DING ◽  
A.B. BONDS ◽  
VIVIEN A. CASAGRANDE
Keyword(s):  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Response Amplitude ◽  
Contrast Threshold ◽  
Peak Response ◽  
V1 Neurons ◽  
Bush Baby ◽  
High Stimulus ◽  
Average Contrast ◽  
Contrast Response

How neurons in the primary visual cortex (V1) of primates process parallel inputs from the magnocellular (M) and parvocellular (P) layers of the lateral geniculate nucleus (LGN) is not completely understood. To investigate whether signals from the two pathways are integrated in the cortex, we recorded contrast-response functions (CRFs) from 20 bush baby V1 neurons before, during, and after pharmacologically inactivating neural activity in either the contralateral LGN M or P layers. Inactivating the M layer reduced the responses of V1 neurons (n = 10) to all stimulus contrasts and significantly elevated (t = 8.15, P < 0.01) their average contrast threshold from 8.04 (± 4.1)% contrast to 22.46 (± 6.28)% contrast. M layer inactivation also significantly reduced (t = 4.06, P < 0.01) the average peak response amplitude. Inactivating the P layer did not elevate the average contrast threshold of V1 neurons (n = 10), but significantly reduced (t = 4.34, P < 0.01) their average peak response amplitude. These data demonstrate that input from the M pathway can account for the responses of V1 neurons to low stimulus contrasts and also contributes to responses to high stimulus contrasts. The P pathway appears to influence mainly the responses of V1 neurons to high stimulus contrasts. None of the cells in our sample, which included cells in all output layers of V1, appeared to receive input from only one pathway. These findings support the view that many V1 neurons integrate information about stimulus contrast carried by the LGN M and P pathways.

Mapping of Stimulus Energy in Primary Visual Cortex

2005 ◽  
Vol 94 (1) ◽  
pp. 788-798 ◽  
Author(s):  
Valerio Mante ◽  
Matteo Carandini
Keyword(s):  
Visual Cortex ◽  
Optical Imaging ◽  
Primary Visual Cortex ◽  
Receptive Fields ◽  
Imaging Study ◽  
Energy Model ◽  
Related Phenomenon ◽  
Population Responses ◽  
Stimulus Energy ◽  
Length Direction

A recent optical imaging study of primary visual cortex (V1) by Basole, White, and Fitzpatrick demonstrated that maps of preferred orientation depend on the choice of stimuli used to measure them. These authors measured population responses expressed as a function of the optimal orientation of long drifting bars. They then varied bar length, direction, and speed and found that stimuli of a same orientation can elicit different population responses and stimuli with different orientation can elicit similar population responses. We asked whether these results can be explained from known properties of V1 receptive fields. We implemented an “energy model” where a receptive field integrates stimulus energy over a region of three-dimensional frequency space. The population of receptive fields defines a volume of visibility, which covers all orientations and a plausible range of spatial and temporal frequencies. This energy model correctly predicts the population response to bars of different length, direction, and speed and explains the observations made with optical imaging. The model also readily explains a related phenomenon, the appearance of motion streaks for fast-moving dots. We conclude that the energy model can be applied to activation maps of V1 and predicts phenomena that may otherwise appear to be surprising. These results indicate that maps obtained with optical imaging reflect the layout of neurons selective for stimulus energy, not for isolated stimulus features such as orientation, direction, and speed.

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