Inhibitory mechanisms are known to be crucial in motor control, epilepsy, anaesthesia, and many other normal and abnormal aspects of a neural function. At present, however, analyses of inhibitory mechanisms are complicated by uncertainties concerning the anatomy of inhibitory circuits, the location of inhibitory synapses on postsynaptic neurons, and the candidate neurotransmitters used by different kinds of inhibitory interneurons. In the segmental motor system two of the major inhibitory inputs to motoneurons are mediated by identifiable interneurons - Renshaw cells (mediating recurrent inhibition) and Ia inhibitory interneurons (mediating reciprocal inhibition). The continuing long term goal of this proposal is to better understand the physiological role of Renshaw cells. To achieve this, it is necessary to compare their properties with the mechanisms of action of at least one other inhibitory input to motoneurons. The Ia inhibitory interneurons are good candidates for this purpose as their own activity is modulated by Renshaw cell actions, thus directly linking the two systems in controlling motor output. The experiments will use techniques which combine intracellular recording and staining of identified inhibitory interneurons and their postsynaptic targets, and subsequent analysis, using light and electron microscopy and postembedding immunogold techniques.
The specific aims are to continue the detailed analysis of Renshaw cell connections to motorneurons, with particular emphasis on how topography and motoneuron type might influence the incidence and distribution of the inhibitory synapses. A similar type of study will be performed on the Ia inhibitory system. For both inhibitory systems, detailed ultrastructural and immunocytochemical analyses will be performed to determine their synaptic relationships and putative neurotransmitters.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
7R01NS025547-06
Application #
3410807
Study Section
Neurology B Subcommittee 2 (NEUB)
Project Start
1992-09-01
Project End
1994-06-30
Budget Start
1992-09-01
Budget End
1993-06-30
Support Year
6
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Wright State University
Department
Type
Schools of Medicine
DUNS #
City
Dayton
State
OH
Country
United States
Zip Code
45435
Romer, Shannon H; Dominguez, Kathleen M; Gelpi, Marc W et al. (2014) Redistribution of Kv2.1 ion channels on spinal motoneurons following peripheral nerve injury. Brain Res 1547:1-15
Couchman, Kiri; Garrett, Andrew; Deardorff, Adam S et al. (2011) Lateral superior olive function in congenital deafness. Hear Res 277:163-75
Leao, Katarina E; Leao, Richardson N; Deardorff, Adam S et al. (2010) Sound stimulation modulates high-threshold K(+) currents in mouse auditory brainstem neurons. Eur J Neurosci 32:1658-67
Gagnon, Kenneth B E; Adragna, Norma C; Fyffe, Robert E W et al. (2007) Characterization of glial cell K-Cl cotransport. Cell Physiol Biochem 20:121-30
Gagnon, Kenneth Be; Fyffe, Robert Ew; Adragna, Norma C et al. (2007) Characterization of an extracellular epitope antibody to the neuronal K-Cl cotransporter, KCC2. Clin Exp Pharmacol Physiol 34:566-73
Walmsley, Bruce; Berntson, Amy; Leao, Richardson N et al. (2006) Activity-dependent regulation of synaptic strength and neuronal excitability in central auditory pathways. J Physiol 572:313-21
Leao, Richardson N; Sun, Hong; Svahn, Katarina et al. (2006) Topographic organization in the auditory brainstem of juvenile mice is disrupted in congenital deafness. J Physiol 571:563-78
Deng, Zhihui; Fyffe, Robert E W (2004) Expression of P2X7 receptor immunoreactivity in distinct subsets of synaptic terminals in the ventral horn of rat lumbar spinal cord. Brain Res 1020:53-61
Wang, Ling; Fyffe, Robert E W; Lu, Luo (2004) Identification of a Kv3.4 channel in corneal epithelial cells. Invest Ophthalmol Vis Sci 45:1796-803
Leao, Richardson N; Oleskevich, Sharon; Sun, Hong et al. (2004) Differences in glycinergic mIPSCs in the auditory brain stem of normal and congenitally deaf neonatal mice. J Neurophysiol 91:1006-12

Showing the most recent 10 out of 33 publications