The long term objective of this project is to further examine these specific changes to identify basic mechanisms responsible for the plasticity observed in the dorsal horn after regeneration of severed nerves. Combined electrophysiological and anatomical methodology coupled with single fiber recording and stimulation techniques will be used to determine: 1) if the population of sprouting fibers make aberrant connections with dorsal horn cells and/or if any properties unique to them can be identified; 2) what specific spinal mechanisms are involved in reconstruction of concise dorsal horn cell receptive fields; 3) if formation of new functional connections aid in the consolidation of dorsal horn cell receptive fields; 4) if more detailed analysis of the integration of somatosensory inputs in intact preparations can enhance our knowledge of these plastic events. The information obtained should enable the identification of specific mechanisms involved in the observed plasticity. Once identified these mechanisms can then be studied further to determine if certain manipulations could perhaps reduce the inappropriate collateral sprouting or enhance the ability of dorsal horn cells to construct concise receptive fields.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS023725-13
Application #
2714455
Study Section
Neurology B Subcommittee 2 (NEUB)
Program Officer
Chiu, Arlene Y
Project Start
1989-09-01
Project End
1999-11-30
Budget Start
1998-06-01
Budget End
1999-11-30
Support Year
13
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Biology
Type
Schools of Medicine
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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