Spinal alpha-motoneurons (""""""""the final common path"""""""") translate a large, complex inflow of synaptic signald from segmentsl and descending fibers and interneurons into a precise output neecessary to maintain posture and initiate movement. In particular motoneurons must intergate information from both """"""""fast"""""""" trasmitters and """"""""slow"""""""" tansmittrs, such as monoamines and peptides which use several different transduction mechanisms (""""""""second messengers"""""""") to influence motoneuron excitability. The process is even more complicated becaues """"""""slow"""""""" transmitters appear able to modulate the effects of """"""""fast"""""""" transmitters. The overall objective of the present investigations is to elucidate some of the complex, interconnected mechanisms by which motoneurons are affected by transmitters putatively released by descending and segmental sources. If dysfunction of synaptic mechanism contorlling motoneurons occurs one would not expect normal spinal cord function. And indeed, abnormalities of motoneuron funcion are imlicated in teh excessive response to passive movement in spasticity, in the absence of reflexes in spinal shock, in the flexor spasms of paraplegia, and in teh pathogenesis of tetanus. Thus, the proposed investigations pertain not only to an imporant area of neurobiology, but are also relevant to understanding the mechanisms of, and ultimately to adequatnely treat, several pathological problems. In exploring synaptic factors taht influence the properties of motoneurons, intra-and extracellular electrophysiological and pharmacological techniques will be used to manipulate and record from frog spinal motoneurons maintained in vitro. These technoiques will be used to test hypotheses taht he output of the motoneuron is governed by compelx pharmacological processes such as the modulatory actions of monoamines and peptides, that these modualtory processes involve multiple receptors and coupling, transduction, and ionic mechanisms, and that jmonoamines and peptides affect the function of mroe classical amino acid transmitters. it is anticipated taht these effeorts will result in a clearer understanding of some of the factors that detrmine how various neurotransmitter and modulator inputs are converted into motoneuron output.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS017577-13
Application #
2263227
Study Section
Neurology B Subcommittee 2 (NEUB)
Project Start
1981-09-01
Project End
1996-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
13
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Miami School of Medicine
Department
Neurology
Type
Schools of Medicine
DUNS #
City
Miami
State
FL
Country
United States
Zip Code
33146
Hackman, J C; Holohean, A M; Davidoff, R A (1997) Role of metabotropic glutamate receptors in the depression of GABA-mediated depolarization of frog primary afferent terminals. Neuroscience 81:1079-90
Valeyev, A Y; Hackman, J C; Wood, P M et al. (1996) Pharmacologically novel GABA receptor in human dorsal root ganglion neurons. J Neurophysiol 76:3555-8
Holohean, A M; Rodriguez, C A; Hackman, J C et al. (1996) Voltage-gated calcium currents in whole-cell patch-clamped bullfrog dorsal root ganglion cells: effects of cell size and intracellular solutions. Brain Res 711:138-45
Holohean, A M; Hackman, J C; Davidoff, R A (1995) Modulation of frog spinal cord interneuronal activity by activation of 5-HT3 receptors. Brain Res 704:184-90
Dalo, N L; Hackman, J C; Storey, K et al. (1995) Changes in motoneuron membrane potential and reflex activity induced by sudden cooling of isolated spinal cords: differences among cold-sensitive, cold-resistant and freeze-tolerant amphibian species. J Exp Biol 198:1765-74
Mash, D C; Staley, J K; Pablo, J P et al. (1995) Properties of ibogaine and its principal metabolite (12-hydroxyibogamine) at the MK-801 binding site of the NMDA receptor complex. Neurosci Lett 192:53-6
Shope, S B; Hackman, J C; Holohean, A M et al. (1993) Activation of alpha-adrenoceptors indirectly facilitates sodium pumping in frog motoneurons. Brain Res 630:207-13
Holohean, A M; Hackman, J C; Shope, S B et al. (1992) Activation of 5-HT1C/2 receptors depresses polysynaptic reflexes and excitatory amino acid-induced motoneuron responses in frog spinal cord. Brain Res 579:8-16
Holohean, A M; Hackman, J C; Shope, S B et al. (1992) Serotonin1A facilitation of frog motoneuron responses to afferent stimuli and to N-methyl-D-aspartate. Neuroscience 48:469-77
Davidoff, R A (1992) Skeletal muscle tone and the misunderstood stretch reflex. Neurology 42:951-63

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