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Type: Journal article
Title: Metabotropic glutamate receptors inhibit mechanosensitivity in vagal sensory neurons
Author: Page, A.
Young, R.
Martin, C.
Umaerus, M.
O'Donnell, T.
Isaacs, N.
Coldwell, J.
Hulander, M.
Mattsson, J.
Lehmann, A.
Blackshaw, L.
Citation: Gastroenterology, 2005; 128(2):402-410
Publisher: W B Saunders Co
Issue Date: 2005
ISSN: 0016-5085
Statement of
Amanda J. Page, Richard L. Young, Chris M. Martin, Mia Umaerus, Tracey A. O’Donnell, Nicole J. Cooper, Jonathan R. Coldwell, Malin Hulander, Jan P. Mattsson, Anders Lehmann and L. Ashley Blackshaw
Abstract: <h4>Background and aims</h4>Inhibitory G-protein-coupled receptors have demonstrated potential in treatment of gastroesophageal reflux disease (GERD) through actions on vagal afferent signaling. Metabotropic glutamate receptors (mGluR) belong to this receptor family and have great pharmacologic and molecular diversity, with 8 subtypes. We investigated mGluR in the vagal system of humans and other species.<h4>Methods</h4>Expression of mGluR1-8 in human, dog, ferret, and rodent nodose ganglia was investigated by reverse-transcription polymerase chain reaction. mGluR1-8 immunohistochemistry was performed in combination with retrograde tracing of vagal afferents from ferret proximal stomach to nodose ganglia. Transport of mGluR peripherally was investigated by vagal ligation, followed by immunohistochemistry. Glutamate receptor pharmacology of ferret and rodent gastroesophageal vagal afferents was investigated by testing single fiber responses to graded mechanical stimuli during drug application to their peripheral endings.<h4>Results</h4>Messenger RNA for several mGluR was detected in the nodose ganglia of all species. Retrograde tracing indicated that ferret gastric vagal afferents express mGluR protein. Accumulation of immunoreactivity proximal to a ligature showed that mGluR were transported peripherally in the vagus nerves. Glutamate (1-30 mumol/L with kynurenate 0.1 mmol/L) concentration dependently inhibited vagal afferent mechanosensitivity. This was mimicked by selective group II and III mGluR agonists but not by a group I agonist. Conversely, a group III mGluR antagonist increased mechanosensitivity to intense stimuli.<h4>Conclusions</h4>Both exogenous and endogenous glutamate inhibits mechanosensitivity of vagal afferents. Group II (mGluR2 and 3) and group III mGluR (mGluR4, 6, 7, 8) are novel targets for inhibition of vagal signaling with therapeutic potential in, for example, GERD.
Keywords: Nodose Ganglion
Afferent Pathways
Neurons, Afferent
Vagus Nerve
Receptors, Metabotropic Glutamate
DNA Primers
Polymerase Chain Reaction
Base Sequence
Description: Copyright © 2005 American Gastroenterological Association Published by Elsevier Inc.
DOI: 10.1053/j.gastro.2004.11.062
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Appears in Collections:Aurora harvest 6
Molecular and Biomedical Science publications

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