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Functionally independent columns of rat somatosensory barrel cortex revealed with voltage-sensitive dye imaging

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Petersen,  Carl C. H.
Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society;
Whisker Representation, Max Planck Institute for Medical Research, Max Planck Society;

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Sakmann,  Bert
Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society;

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Petersen, C. C. H., & Sakmann, B. (2001). Functionally independent columns of rat somatosensory barrel cortex revealed with voltage-sensitive dye imaging. The Journal of Neuroscience: the Official Journal of the Society for Neuroscience, 21(21), 8435-8446. Retrieved from http://www.jneurosci.org/cgi/content/abstract/21/21/8435.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0028-FD81-E
Abstract
Whisker movement is somatotopically represented in rodent neocortex by electrical activity in clearly defined barrels, which can be visualized in living brain slices. The functional architecture of this part of the cortex can thus be mapped in vitro with respect to its physiological input and compared with its anatomical architecture. The spatial extent of excitation was measured at high temporal resolution by imaging optical signals from voltage-sensitive dye evoked by stimulation of individual barrels in layer 4. The optical signals correlated closely with subthreshold EPSPs recorded simultaneously from excitatory neurons in layer 4 and layer 2/3, respectively. Excitation was initially (<2 msec) limited to the stimulated barrel and subsequently (>3 msec) spread in a columnar manner into layer 2/3 and then subsided in both layers after ∼50 msec. The lateral extent of the response was limited to the cortical column defined structurally by the barrel in layer 4. Two experimental interventions increased the spread of excitation. First, blocking GABAA receptor-mediated synaptic inhibition caused excitation to spread laterally throughout wide regions of layer 2/3 and layer 5 but not into neighboring barrels, suggesting that the local excitatory connections within layer 4 are restricted to single barrels and that inhibitory neurons control spread in supragranular and infragranular layers. Second, NMDA receptor-dependent increase of the spread of excitation was induced by pairing repetitive stimulation of a barrel column with coincident stimulation of layer 2/3 in a neighboring column. Such plasticity in the spatial extent of excitation in a barrel column could underlie changes in cortical map structure induced by alterations of sensory experience.