Visceral sensory neurons of the vagus and glossopharyngeal nerves innervate the major organ systems of the thorax and abdomen. These afferent neurons transmit information concerning such diverse stimuli as blood pressure, gastric distention, bronchiolar irritation and blood oxygenation to the CNS. The objective of this project is to define the chemical neuroanatomy of these visceral sensory neurons which are located in the nodose and petrosal ganglia. This includes studies of neurotransmitters, their distribution and correlation with CNS and peripheral projections, neurotransmitter co-existence, and the regulation of transmitter content and expression. Our current hypothesis proposes that visceral sensory neurons of the nodose and petrosal ganglia use multiple neurotransmitters and combinations of co-existence transmitters, and that the expression of transmitter in individual neurons is dependent upon the level of neuronal activity, and upon the target organ of innervation. Evidence for or against this hypothesis will be obtained by studying transmitter co-existence in the nodose and petrosal ganglia, determining patterns of co- existence in relation to the organ of innervation, localizing mRNA which encodes for precursors of the neurotransmitters, and subsequently determining whether changes in transmitter content or mRNA levels occur in visceral afferent neurons following changes in neuronal activity of connectivity. The techniques used in these studies include: immunocytochemistry retrograde tracing techniques, in situ hybridization histochemistry, neurotransmitter assays, and in vivo pharmacological approaches. These studies will provide information on the cellular neurobiology of transmitter systems in visceral sensory neurons which will be useful in the understanding and treatment of derangements of the autonomic control of the cardiovascular, respiratory, and gastrointestinal systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS020991-08
Application #
3401702
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1984-09-30
Project End
1994-08-31
Budget Start
1992-12-01
Budget End
1994-08-31
Support Year
8
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Henry M. Jackson Fdn for the Adv Mil/Med
Department
Type
DUNS #
City
Rockville
State
MD
Country
United States
Zip Code
20817
Lee, P; Zhuo, H; Helke, C J (2001) Axotomy alters neurotrophin and neurotrophin receptor mRNAs in the vagus nerve and nodose ganglion of the rat. Brain Res Mol Brain Res 87:31-41
Helke, C J; Verdier-Pinard, D (2000) Neurotrophins alter the numbers of neurotransmitter-ir mature vagal/glossopharyngeal visceral afferent neurons in vitro. Brain Res 884:206-12
Ichikawa, H; Helke, C J (1999) The coexistence of TrkA with putative transmitter agents and calcium-binding proteins in the vagal and glossopharyngeal sensory neurons of the adult rat. Brain Res 846:268-73
Ichikawa, H; Helke, C J (1998) Coexistence of s100beta and putative transmitter agents in vagal and glossopharyngeal sensory neurons of the rat. Brain Res 800:312-8
Helke, C J; Adryan, K M; Fedorowicz, J et al. (1998) Axonal transport of neurotrophins by visceral afferent and efferent neurons of the vagus nerve of the rat. J Comp Neurol 393:102-17
Ichikawa, H; Helke, C J (1997) Coexistence of calcium-binding proteins in vagal and glossopharyngeal sensory neurons of the rat. Brain Res 768:349-53
Zhuo, H; Ichikawa, H; Helke, C J (1997) Neurochemistry of the nodose ganglion. Prog Neurobiol 52:79-107
Zhuo, H; Helke, C J (1996) Presence and localization of neurotrophin receptor tyrosine kinase (TrkA, TrkB, TrkC) mRNAs in visceral afferent neurons of the nodose and petrosal ganglia. Brain Res Mol Brain Res 38:63-70
Ichikawa, H; Helke, C J (1996) Coexistence of calbindin D-28k and NADPH-diaphorase in vagal and glossopharyngeal sensory neurons of the rat. Brain Res 735:325-9
Ichikawa, H; Helke, C J (1995) Parvalbumin and calbindin D-28k in vagal and glossopharyngeal sensory neurons of the rat. Brain Res 675:337-41

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