The examination of the roles of afferent and muscle activity in regulating la afferent-motoneuron (la-MN) synaptic strength will contribute to the long-term goal of understanding synaptic physiology in the adult mammalian central nervous system. The la-MN synapse is a glutamatergic synapse in the spinal cord. Previous studies have shown that blocking action potential activity in a peripheral nerve increases the la-MN synaptic strength of the treated nerve. In these experiments a neurotoxin (TTX), was locally administered to a portion of the sciatic nerve in the hind limb. The toxin eliminated afferent and motor activity in the treated nerve; and resulted in increased la-MN synaptic strength.
The specific aims of this research proposal are to elucidate the factors that normally constrain synaptic strength at the la-MN synapse. Specifically, we ask whether the maintenance of impulse-evoked afferent activity can prevent or reduce the increase otherwise observed with TTX treatment alone and whether the maintenance of muscle activity can prevent or reduce the increase in la-MN synaptic strength. These data will provide insight into the factors that regulate synaptic strength in the central nervous system of adult mammals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31NS046982-01A1
Application #
6792358
Study Section
Special Emphasis Panel (ZRG1-F02B (20))
Program Officer
Talley, Edmund M
Project Start
2004-05-01
Project End
2006-04-30
Budget Start
2004-05-01
Budget End
2005-04-30
Support Year
1
Fiscal Year
2004
Total Cost
$41,774
Indirect Cost
Name
Emory University
Department
Physiology
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Bichler, Edyta K; Nakanishi, Stan T; Wang, Qing-Bo et al. (2007) Enhanced transmission at a spinal synapse triggered in vivo by an injury signal independent of altered synaptic activity. J Neurosci 27:12851-9