Neuronal populations in motor areas of cerebral cortex that act as input to the basal ganglia will be identified by retrograde transport of tritiated acetyl wheat germ agglutinin or wheat germ agglutinin conjegated to horseradish peroxidase. Paired injections in neostriatum and each of several other major targets of motor and premotor cortex will also be performed. The neurons projecting to neostriatum will be compared to those giving rise to other important motor cortex output pathways, and the extent to which neurons in cerebral cortex have branched axons projecting to neostriatum and another structure will be assessed. Corticostriatal neurons from each of the populations defined in this way will also be identified by antidromic activation in intracellular recording experiments. These cells will be stained by intracellular injection of horseradish peroxidase to examine their dendritic branching patterns (as an indication of what inputs they might receive), their patterns of intracortical synaptic connections (inferred from the distribution of their intracortical axonal arborizations) and the size and shape of the area in neostriatum that receives an input from a single axon. In addition, major inputs to these cortical areas will be stimulated and the responses of intracellularly recorded corticostriatal neurons analyzed to determine the extent to which different populations of corticostriatal neurons receive synaptic input from ventral thalamic nuclei, contralateral motor and premotor cortex, and axon collaterals of pyramidal tract neurons. These experiments are designed to help to define the nature of the motor cortex input to the basal ganglia by comparing the neurons that convey it to those carrying cortical efferent activity in pathways whose behavioral importance is more clearly understood. They will also contribute to the process of defining the operations performed by the basal ganglia on its cortical input.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS020743-03
Application #
3401300
Study Section
Neurology B Subcommittee 1 (NEUB)
Project Start
1983-08-01
Project End
1988-08-31
Budget Start
1986-09-01
Budget End
1987-08-31
Support Year
3
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Tennessee Health Science Center
Department
Type
Schools of Medicine
DUNS #
941884009
City
Memphis
State
TN
Country
United States
Zip Code
38163
Sachdev, Robert N S; Ebner, Ford F; Wilson, Charles J (2004) Effect of subthreshold up and down states on the whisker-evoked response in somatosensory cortex. J Neurophysiol 92:3511-21
Tepper, James M; Koos, Tibor; Wilson, Charles J (2004) GABAergic microcircuits in the neostriatum. Trends Neurosci 27:662-9
Koos, Tibor; Tepper, James M; Wilson, Charles J (2004) Comparison of IPSCs evoked by spiny and fast-spiking neurons in the neostriatum. J Neurosci 24:7916-22
Reiner, A; Stern, E A; Wilson, C J (2001) Physiology and morphology of intratelencephalically projecting corticostriatal-type neurons in pigeons as revealed by intracellular recording and cell filling. Brain Behav Evol 58:101-14
Wickens, J R; Wilson, C J (1998) Regulation of action-potential firing in spiny neurons of the rat neostriatum in vivo. J Neurophysiol 79:2358-64
Kincaid, A E; Wilson, C J (1996) Corticostriatal innervation of the patch and matrix in the rat neostriatum. J Comp Neurol 374:578-92
da Costa Gomez, T M; Behbehani, M M (1995) An electrophysiological characterization of the projection from the central nucleus of the amygdala to the periaqueductal gray of the rat: the role of opioid receptors. Brain Res 689:21-31
Wilson, C J (1994) Understanding the neostriatal microcircuitry: high-voltage electron microscopy. Microsc Res Tech 29:368-80
Cowan, R L; Wilson, C J (1994) Spontaneous firing patterns and axonal projections of single corticostriatal neurons in the rat medial agranular cortex. J Neurophysiol 71:17-32
Jaeger, D; Kita, H; Wilson, C J (1994) Surround inhibition among projection neurons is weak or nonexistent in the rat neostriatum. J Neurophysiol 72:2555-8

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