Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12890
Title: Reduced glutamate binding in rat dorsal vagal complex after nodose ganglionectomy.
Austin Authors: Lewis, S J;Verberne, Anthony J M ;Summers, R J;Beart, P M;Cincotta, M
Affiliation: University of Melbourne, Clinical Pharmacology and Therapeutics Unit, Austin Hospital, Heidelberg, Victoria, Australia
Issue Date: 1-Dec-1988
Publication information: Brain Research Bulletin; 21(6): 913-6
Abstract: Quantitative receptor autoradiography with L-[3H]glutamate was employed to examine the distribution and properties of glutamate binding sites in the rat brain 14 days after excision of the right nodose ganglion. Slide-mounted coronal sections of the brain showed reduced L-[3H]glutamate binding in the nucleus tractus solitarius/dorsal motor nucleus of the vagus in the ipsilateral relative to the sham-operated side. Densitometric and saturation analyses of binding data indicated a significant reduction in the density of glutamate binding sites (57% decrease relative to sham), while there was a significant increase in receptor affinity (40% greater than sham). Binding was unaltered in the inferior olivary complex. Glutamate receptors are likely to exist on synaptic nerve terminals of vagal afferent fibres within the nucleus tractus solitarius and on vagal preganglionic neurones within the dorsal motor nucleus of the vagus and/or their dendritic processes within the nucleus tractus solitarius. Additionally, our receptor autoradiographic studies provide evidence for L-glutamate being a transmitter of vagal afferent neurones.
Gov't Doc #: 2906272
URI: http://ahro.austin.org.au/austinjspui/handle/1/12890
URL: https://pubmed.ncbi.nlm.nih.gov/2906272
Type: Journal Article
Subjects: Animals
Autoradiography
Female
Glutamates.metabolism
Glutamic Acid
Nodose Ganglion.metabolism
Rats
Rats, Inbred Strains
Receptors, Glutamate
Receptors, Neurotransmitter.metabolism
Vagus Nerve.metabolism
Appears in Collections:Journal articles

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