The proper functioning of oral-facial motor behaviors is necessary for the survival of humans. The ingestive behaviors of mammals begins with suckling and progresses to drinking and feeding. Presently, there are very few studies addressing how the brain is organized to produce these behaviors. Even less is known about the etiology of various oral-motor dysfunctions such as tardive dyskinesia. bruxism, and myofacial pain dysfunction syndromes. The long-term goals of this research are to understand both the mechanism underlying the central nervous system control of normal jaw movements that occur during activities such as feeding and drinking, as well as the abnormal jaw movements that occur during various disorders.
The specific aims of this proposal are to continue investigations, at the cellular level, into the neuronal processes controlling jaw movements in the guinea pig. We will combine intracellular or whole cell patch clamp recording methods with retrograde-tract tracing techniques to identify specific populations of jaw-opener and closer motoneurons, and trigeminal premotoneurons in thin and thick brain slices. The project is divided into two main parts. In part I, we will determine for identified jaw-opener and closer motoneurons and premotoneurons, I) the presence of specific intrinsic membrane conductances and their contribution to neuronal burst discharge, 2) whether these conductances are substrates for modulation by two monoamines (5-HT and NE). Part II will focus on modulation of excitatory amino acid mediated synaptic transmission by monoamines. We will determine if there are fundamental similarities and differences in modulation by serotonin and norepinephrine between NMDA and non-NMDA components of synaptic transmission to trigeminal motoneurons from mesencephalic of V afferents (Mes V). We will examine these relationships by recording the compound EPSP or EPSC and the single fiber EPSP or EPSC evoked from Mes V nucleus or single Mes V neuron stimulation, respectively. The results of the proposed studies will provide insights into the cellular mechanisms controlling discharge of distinct populations of neurons involved in production of jaw movements and will serve as a cellular foundation for neuronal models on masticatory rhythm and burst pattern generation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE006193-16
Application #
2749303
Study Section
Neurology B Subcommittee 2 (NEUB)
Project Start
1983-08-01
Project End
2002-07-31
Budget Start
1998-08-01
Budget End
1999-07-31
Support Year
16
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Physiology
Type
Schools of Arts and Sciences
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Tsuruyama, Kentaro; Hsiao, Chie-Fang; Chandler, Scott H (2013) Participation of a persistent sodium current and calcium-activated nonspecific cationic current to burst generation in trigeminal principal sensory neurons. J Neurophysiol 110:1903-14
Hsiao, Chie-Fang; Kaur, Gurvinder; Vong, Angela et al. (2009) Participation of Kv1 channels in control of membrane excitability and burst generation in mesencephalic V neurons. J Neurophysiol 101:1407-18
Hsiao, Chie-Fang; Gougar, Kelly; Asai, J et al. (2007) Intrinsic membrane properties and morphological characteristics of interneurons in the rat supratrigeminal region. J Neurosci Res 85:3673-86
Enomoto, Akifumi; Han, Juliette M; Hsiao, Chie-Fang et al. (2007) Sodium currents in mesencephalic trigeminal neurons from Nav1.6 null mice. J Neurophysiol 98:710-9
Enomoto, Akifumi; Han, Juliette M; Hsiao, Chie-Fang et al. (2006) Participation of sodium currents in burst generation and control of membrane excitability in mesencephalic trigeminal neurons. J Neurosci 26:3412-22
Tanaka, Susumu; Chandler, Scott H (2006) Serotonergic modulation of persistent sodium currents and membrane excitability via cyclic AMP-protein kinase A cascade in mesencephalic V neurons. J Neurosci Res 83:1362-72
Wu, Nanping; Enomoto, Akifumi; Tanaka, Susumu et al. (2005) Persistent sodium currents in mesencephalic v neurons participate in burst generation and control of membrane excitability. J Neurophysiol 93:2710-22
Hsiao, Chie-Fang; Wu, Nanping; Chandler, Scott H (2005) Voltage-dependent calcium currents in trigeminal motoneurons of early postnatal rats: modulation by 5-HT receptors. J Neurophysiol 94:2063-72
Tanaka, Susumu; Wu, Nanping; Hsaio, Chie-Fang et al. (2003) Development of inward rectification and control of membrane excitability in mesencephalic v neurons. J Neurophysiol 89:1288-98
Hsiao, Chie-Fang; Wu, Nanping; Levine, Michael S et al. (2002) Development and serotonergic modulation of NMDA bursting in rat trigeminal motoneurons. J Neurophysiol 87:1318-28

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