Manipulations will be studied that (1) modify the processing of sensory input in the spinal cord dorsal horn, and (2) are accompanied by pronounced abnormalities of somatosensory perception in animals and humans. The goals are to detect and quantitatively characterize the effects of each manipulation on the differential responses of normal contralateral SI cortex to precisely controlled mechanical vs. thermal stimulation of the skin. Anesthetized squirrel monkeys will serve as subjects. The methods of near-infrared optical intrinsic signal (OIS) imaging and extracellular microelectrode recording of spike discharge activity will be used to characterize (both before and after each manipulation) the SI responses to thermal and mechanical stimulation of the skin at both the neuron population and single neuron levels of analysis. The project is expected to (1) reveal a hitherto unappreciated sensitivity of the SI cortical response evoked by natural skin stimuli to manipulations that modify the processing of sensory input by spinal cord dorsal horn neurons; and (2) establish the extent to which the altered SI response to natural skin stimuli can be attenuated/reversed by selective ablation of NK-1 (Substance P) receptor expressing neurons in the superficial dorsal horn of the spinal cord, or by the selective block of spinal cord NMDA receptors.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS037501-05
Application #
6845726
Study Section
Somatosensory and Chemosensory Systems Study Section (SCS)
Program Officer
Chen, Daofen
Project Start
2000-04-01
Project End
2008-03-31
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
5
Fiscal Year
2005
Total Cost
$316,350
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Physiology
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Lee, Jaekwang; Han, Young-Eun; Favorov, Oleg et al. (2016) Fluoride Induces a Volume Reduction in CA1 Hippocampal Slices Via MAP Kinase Pathway Through Volume Regulated Anion Channels. Exp Neurobiol 25:72-8
Lee, Jaekwang; Woo, Junsung; Favorov, Oleg V et al. (2012) Columnar distribution of activity dependent gabaergic depolarization in sensorimotor cortical neurons. Mol Brain 5:33
Whitsel, B L; Favorov, O V; Li, Y et al. (2010) Nociceptive afferent activity alters the SI RA neuron response to mechanical skin stimulation. Cereb Cortex 20:2900-15
Whitsel, Barry L; Favorov, Oleg V; Li, Yongbiao et al. (2009) Area 3a neuron response to skin nociceptor afferent drive. Cereb Cortex 19:349-66
Tommerdahl, M; Tannan, V; Cascio, C J et al. (2007) Vibrotactile adaptation fails to enhance spatial localization in adults with autism. Brain Res 1154:116-23
Lee, Jaekwang; Tommerdahl, M; Favorov, O V et al. (2005) Optically recorded response of the superficial dorsal horn: dissociation from neuronal activity, sensitivity to formalin-evoked skin nociceptor activation. J Neurophysiol 94:852-64
Tommerdahl, M; Hester, K D; Felix, E R et al. (2005) Human vibrotactile frequency discriminative capacity after adaptation to 25 Hz or 200 Hz stimulation. Brain Res 1057:1-9
Whitsel, B L; Kelly, E F; Quibrera, M et al. (2003) Time-dependence of SI RA neuron response to cutaneous flutter stimulation. Somatosens Mot Res 20:45-69
Tommerdahl, Mark; Favorov, Oleg; Whitsel, Barry L (2002) Optical imaging of intrinsic signals in somatosensory cortex. Behav Brain Res 135:83-91
Kohn, Adam; Whitsel, Barry L (2002) Sensory cortical dynamics. Behav Brain Res 135:119-26

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