This proposal will characterize the postnatal development of the genioglossal and phrenic motoneurons, by correlating physiological changes in membrane conductance and spiking properties with changes in anatomy. The strength of respiratory muscle contraction is determined by the number of respiratory motoneurons activated and their rate of discharge. Both the order in which the neurons are activated and their discharge rates are a function of their resting conductance, that is, the number of membrane channels open at any given time. Most membrane channels are controlled by neurotransmitters and/or by the intrinsic electrical state of the cell membrane. The change in the balance of these two processes are most dramatic during postnatal development. The applicant is interested in these processes that occur in the two respiratory motoneurons that affect the performance of the diaphragm and genioglossus. Activation of these two muscles must be coordinated to move air into the lungs with the least effort; this may be particularly relevant to the pathophysiology of Sudden Infant Death Syndrome (SIDS). In the past period, the applicant established that glycine significantly contributed to the increase in resting membrane conductance that occurs at 3 weeks, and that these age-related increases in resting conductance result from an increase in the number of open potassium channels. The proposed studies will be performed on genioglossal and phrenic motoneurons in slice preparations of the rat brainstem and spinal cord. Visually identified motoneurons will be studied from four different age groups (1-2, 5-7, 13-15 and 19-22 days) with a combination of patch-clamp recording, three-dimensional neuronal reconstruction and immunocytochemical localization of certain receptors and ion channels. The application will: 1) examine the anatomy and physiology of glycine, GABA, and glutamate neurotransmitter systems at the four stages during postnatal development; 2) identify specific potassium channels that contribute to the increase in membrane conductance and spike characteristics; and 3) explore the intracellular pathways mediating the enhanced potassium conductance.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD022703-19
Application #
6629080
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Program Officer
Willinger, Marian
Project Start
1999-02-01
Project End
2005-01-31
Budget Start
2003-02-01
Budget End
2005-01-31
Support Year
19
Fiscal Year
2003
Total Cost
$213,594
Indirect Cost
Name
Oregon Health and Science University
Department
Physiology
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Carrascal, Livia; Nieto-Gonzalez, Jose Luis; Cameron, William E et al. (2005) Changes during the postnatal development in physiological and anatomical characteristics of rat motoneurons studied in vitro. Brain Res Brain Res Rev 49:377-87
Nunez-Abades, P A; Pattillo, J M; Hodgson, T M et al. (2000) Role of synaptic inputs in determining input resistance of developing brain stem motoneurons. J Neurophysiol 84:2317-29
Robinson, D W; Cameron, W E (2000) Time-dependent changes in input resistance of rat hypoglossal motoneurons associated with whole-cell recording. J Neurophysiol 83:3160-4
Cameron, W E; Nunez-Abades, P A; Kerman, I A et al. (2000) Role of potassium conductances in determining input resistance of developing brain stem motoneurons. J Neurophysiol 84:2330-9
Nunez-Abades, P A; Cameron, W E (1997) Relationship between membrane properties and cell size of developing rat genioglossal motoneurons studied in vitro. Neurosci Lett 223:41-4
Nunez-Abades, P A; Cameron, W E (1995) Morphology of developing rat genioglossal motoneurons studied in vitro: relative changes in diameter and surface area of somata and dendrites. J Comp Neurol 353:129-42
Nunez-Abades, P A; He, F; Barrionuevo, G et al. (1994) Morphology of developing rat genioglossal motoneurons studied in vitro: changes in length, branching pattern, and spatial distribution of dendrites. J Comp Neurol 339:401-20
Nunez-Abades, P A; Spielmann, J M; Barrionuevo, G et al. (1993) In vitro electrophysiology of developing genioglossal motoneurons in the rat. J Neurophysiol 70:1401-11
Mazza, E; Nunez-Abades, P A; Spielmann, J M et al. (1992) Anatomical and electrotonic coupling in developing genioglossal motoneurons of the rat. Brain Res 598:127-37
Cameron, W E; Jodkowski, J S; Fang, H et al. (1991) Electrophysiological properties of developing phrenic motoneurons in the cat. J Neurophysiol 65:671-9

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