Cutaneous primary afferent neurons are complicated cells with specialized sites which include receptors responsible for receiving stimuli and transducing them into electrical potentials, axons capable of conducting to the spinal cord impulses generated in the periphery, and central terminals capable of releasing transmitter onto secondary neurons. The functions of these neurons can be regulated at these sites by various chemical, ionic, or synaptic means. The overall objectives of the present investigations are to understand more fully the mechanisms responsible for regulating the activity of afferent neurons.
These aims follow from results of my recent previous studies which have centered on the control mechanisms affecting afferent terminals; such studies are not only widened, but will now be extended to include the peripheral end of the same cells. The project will continue investigations of the amphibian sensory system in the spinal cord maintained in vitro and will utilize electrophysiological and pharmacological techniques to study different parts of the afferent neuron in isolated preparations. The proposed experiments seek to elucidate the roles various chemicals located in the skin and nerves play in the excitation of nociceptive cutaneous receptors and/or in their sensitization to noxious stimuli. Investigations of this problem will use a skin-nerve preparation to determine the changes in single cutaneous afferents produced by noxious stimuli and by """"""""algesic"""""""" substances. Ion-sensitive microelectrodes inserted in the gray matter of the spinal cord will be used to determine what neuronal elements and/or transmitters are responsible for the rises in extracellular K+ concentration produced by afferent activity and presumably important in regulating the excitability of afferent terminals. Intracellular recording and voltage clamping of afferent cell bodies will be used to ascertain the mechanism of action of catecholamines on the membranes of afferent neurons. The production of pain is a major medical, and human, concern. Thus, the proposed investigations pertain not only to an important area of neurobiology, but are also relevant to understanding the mechanisms of a symptom central to many disease states.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS017577-05
Application #
3397654
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1981-09-01
Project End
1988-11-30
Budget Start
1985-12-01
Budget End
1986-11-30
Support Year
5
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Miami School of Medicine
Department
Type
Schools of Medicine
DUNS #
City
Miami
State
FL
Country
United States
Zip Code
33101
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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