Visual processing in the brain seems to provide fast but coarse information before information about fine details. Such dynamics occur also in single neurons at several levels of the visual system. In the dorsal lateral geniculate nucleus (LGN), neurons have a receptive field (RF) with antagonistic center-surround organization, and temporal changes in center-surround organization are generally assumed to be due to a time-lag of the surround activity relative to center activity. Spatial resolution may be measured as the inverse of center size, and in LGN neurons RF-center width changes during static stimulation with durations in the range of normal fixation periods (250–500 ms) between saccadic eye-movements. The RF-center is initially large, but rapidly shrinks during the first ∼100 ms to a rather sustained size. We studied such dynamics in anesthetized cats during presentation (250 ms) of static spots centered on the RF with main focus on the transition from the first transient and highly dynamic component to the second more sustained component. The results suggest that the two components depend on different neuronal mechanisms that operate in parallel and with partial temporal overlap rather than on a continuously changing center-surround balance. Results from mathematical modeling further supported this conclusion. We found that existing models for the spatiotemporal RF of LGN neurons failed to account for our experimental results. The modeling demonstrated that a new model, in which the response is given by a sum of an early transient component and a partially overlapping sustained component, adequately accounts for our experimental data.
Coarse-to-Fine Changes of Receptive Fields in Lateral Geniculate Nucleus Have a Transient and a Sustained Component That Depend on Distinct Mechanisms
G. Einevoll,P. Jurkus,P. Heggelund
Published 2011 in PLoS ONE
ABSTRACT
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- Publication year
2011
- Venue
PLoS ONE
- Publication date
2011-09-09
- Fields of study
Biology, Medicine, Physics
- Identifiers
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- Source metadata
Semantic Scholar, PubMed
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