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Immunocytochemical localization of glutamic acid decarboxylase (GAD) and substance P in neural areas mediating motion-induced emesis: Effects of vagal stimulation on GAD immunoreactivityImmunocytochemical methods were employed to localize the neurotransmitter amino acid gamma-aminobutyric acid (GABA) by means of its biosynthetic enzyme glutamic acid decarboxylase (GAD) and the neuropeptide substance P in the area postrema (AP), area subpostrema (ASP), nucleus of the tractus solitarius (NTS), and gelatinous nucleus (GEL). In addition, electrical stimulation was applied to the night vagus nerve at the cervical level to assess the effects on GAD-immunoreactivity (GAR-IR).

GAD-IR terminals and fibers were observed in the AP, ASP, NTS, and GEL. They showed pronounced density at the level of the ASP and gradual decrease towards the solitary complex. Nerve cells were not labelled in our preparations. Ultrastructural studies showed symmetric or asymmetric synaptic contracts between labelled terminals and non-immunoreactive dendrites, axons, or neurons. Some of the labelled terminals contained both clear- and dense-core vesicles. Our preliminary findings, after electrical stimulation of the vagus nerve, revealed a bilateral decrease of GAD-IR that was particularly evident at the level of the ASP.

SP-immunoreactive (SP-IR) terminals and fibers showed varying densities in the AP, ASP, NTS, and GEL. In our preparations, the lateral sub-division of the NTS showed the greatest accumulation. The ASP showed medium density of immunoreactive varicosities and terminals and the AP and GEL displayed scattered varicose axon terminals. The electron microscopy revealed that all immunoreactive terminals contained clear-core vesicles which make symmetric or asymmetric synaptic contact with unlabelled dendrites.

It is suggested that the GABAergic terminals might correspond to vagal afferent projections and that GAD/GABA and substance P might be co-localized in the same terminal allowing the possibility of a regulated release of the transmitters in relation to demands.
Document ID
19940017436
Acquisition Source
Ames Research Center
Document Type
Conference Paper
Authors
F D'Amelio
(San Jose State University San Jose, United States)
M A Gibbs
(Ames Research Center Mountain View, United States)
W R Mehler
(Ames Research Center Mountain View, United States)
N G Daunton
(Ames Research Center Mountain View, United States)
R A Fox
(San Jose State University San Jose, United States)
Date Acquired
September 6, 2013
Publication Date
January 1, 1991
Publication Information
Publication: Self-Motion Perception and Motion Sickness
Publisher: National Aeronautics and Space Administration
Subject Category
Life Sciences (General)
Report/Patent Number
NASA-CR-194276
Meeting Information
Meeting: International Symposium on Basic and Applied Aspects of Vestibular Function
Location: Hong Kong
Country: HK
Start Date: September 13, 1987
End Date: September 16, 1987
Sponsors: University of Hong Kong, National Aeronautics and Space Administration
Accession Number
94N21909
Funding Number(s)
CONTRACT_GRANT: NCC2-167
Distribution Limits
Public
Copyright
Public Use Permitted.
Keywords
GABA
substance P
vagus nerve
area posuema
nucleus tracrus solitarius
immunocytochemisiry
electrical stimulation
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