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Response properties of antral mechanosensitive afferent fibers and effects of ionotropic glutamate receptor antagonists

The ionotropic glutamate receptors N-methyl- d-aspartate (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors are present peripherally in the primary sensory afferent neurons innervating the viscera. Multiple studies have reported roles of glutamate receptors in gastric f...

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Published in:Neuroscience 2004, Vol.125 (3), p.711-723
Main Authors: Sengupta, J.N, Petersen, J, Peles, S, Shaker, R
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description The ionotropic glutamate receptors N-methyl- d-aspartate (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors are present peripherally in the primary sensory afferent neurons innervating the viscera. Multiple studies have reported roles of glutamate receptors in gastric functions. However, no study has previously shown the direct influence of ionotropic glutamate receptor antagonist on vagal sensory neurons. The objective of this study was to investigate the effects of NMDA and AMPA receptor antagonists on mechanotransduction properties of vagal afferent fibers innervating the rat stomach. Action potentials were recorded from the hyponodal vagus nerve innervating the antrum of the Long-Evans rats. For antral distension (AD), a small latex balloon was inserted into the stomach and positioned in the antrum. The antral contractions were recorded with solid-state probe inserted into the water-filled balloon. Antral units were identified to isovolumic (0.2–1 ml) or isobaric AD (5–60 mm Hg). NMDA and AMPA receptor antagonists were injected in a cumulative fashion (1–100 μmol/kg, i.v.). After the conclusion of experiment, the abdomen was opened and receptive field was mapped by probing the serosa of the stomach. Thirty-two fibers were identified to AD. The receptive fields of 26 fibers were located in the posterior part of the antrum. All fibers exhibited spontaneous firing (mean: 7.00±0.97 impulses/s). Twenty fibers exhibited a rhythmic firing that was in phase with antral contractions, whereas 12 fibers exhibited non-rhythmic spontaneous firing unrelated to spontaneous antral contraction. Both groups of fibers exhibited a linear increase in responses to graded isovolumic or isobaric distensions. NMDA (memantine HCl and dizocilpine (MK-801)) and AMPA/kainate (6-cyano-7-nitroquinoxaline 2,3-dione; CNQX) receptor antagonists dose-dependently attenuated the mechanotransduction properties of these fibers to AD. However, competitive NMDA antagonist dl-2-amino-5 phosphopentanoic acid (AP-5) had no effect. The study documents that glutamate receptor antagonists can attenuate responses of gastric vagal sensory afferent fibers innervating the distal stomach, offering insight to potential pharmacological agents in the treatment of gastric disorders.
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Multiple studies have reported roles of glutamate receptors in gastric functions. However, no study has previously shown the direct influence of ionotropic glutamate receptor antagonist on vagal sensory neurons. The objective of this study was to investigate the effects of NMDA and AMPA receptor antagonists on mechanotransduction properties of vagal afferent fibers innervating the rat stomach. Action potentials were recorded from the hyponodal vagus nerve innervating the antrum of the Long-Evans rats. For antral distension (AD), a small latex balloon was inserted into the stomach and positioned in the antrum. The antral contractions were recorded with solid-state probe inserted into the water-filled balloon. Antral units were identified to isovolumic (0.2–1 ml) or isobaric AD (5–60 mm Hg). NMDA and AMPA receptor antagonists were injected in a cumulative fashion (1–100 μmol/kg, i.v.). 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Psychology</topic><topic>Glutamic Acid - metabolism</topic><topic>Male</topic><topic>mechanoreceptors</topic><topic>Mechanoreceptors - drug effects</topic><topic>Mechanoreceptors - metabolism</topic><topic>Mechanotransduction, Cellular - drug effects</topic><topic>Mechanotransduction, Cellular - physiology</topic><topic>motility</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle, Smooth - drug effects</topic><topic>Muscle, Smooth - physiology</topic><topic>Neurons, Afferent - drug effects</topic><topic>Neurons, Afferent - metabolism</topic><topic>NMDA</topic><topic>Physical Stimulation - instrumentation</topic><topic>Physical Stimulation - methods</topic><topic>Pyloric Antrum - drug effects</topic><topic>Pyloric Antrum - innervation</topic><topic>Pyloric Antrum - physiology</topic><topic>Rats</topic><topic>Rats, Long-Evans</topic><topic>Receptors, AMPA - antagonists &amp; inhibitors</topic><topic>Receptors, AMPA - metabolism</topic><topic>Receptors, Glutamate - drug effects</topic><topic>Receptors, Glutamate - metabolism</topic><topic>Receptors, N-Methyl-D-Aspartate - antagonists &amp; inhibitors</topic><topic>Receptors, N-Methyl-D-Aspartate - metabolism</topic><topic>vagus</topic><topic>Vagus Nerve - drug effects</topic><topic>Vagus Nerve - physiology</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Visceral Afferents - drug effects</topic><topic>Visceral Afferents - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sengupta, J.N</creatorcontrib><creatorcontrib>Petersen, J</creatorcontrib><creatorcontrib>Peles, S</creatorcontrib><creatorcontrib>Shaker, R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sengupta, J.N</au><au>Petersen, J</au><au>Peles, S</au><au>Shaker, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Response properties of antral mechanosensitive afferent fibers and effects of ionotropic glutamate receptor antagonists</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2004</date><risdate>2004</risdate><volume>125</volume><issue>3</issue><spage>711</spage><epage>723</epage><pages>711-723</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>The ionotropic glutamate receptors N-methyl- d-aspartate (NMDA) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors are present peripherally in the primary sensory afferent neurons innervating the viscera. Multiple studies have reported roles of glutamate receptors in gastric functions. However, no study has previously shown the direct influence of ionotropic glutamate receptor antagonist on vagal sensory neurons. The objective of this study was to investigate the effects of NMDA and AMPA receptor antagonists on mechanotransduction properties of vagal afferent fibers innervating the rat stomach. Action potentials were recorded from the hyponodal vagus nerve innervating the antrum of the Long-Evans rats. For antral distension (AD), a small latex balloon was inserted into the stomach and positioned in the antrum. The antral contractions were recorded with solid-state probe inserted into the water-filled balloon. Antral units were identified to isovolumic (0.2–1 ml) or isobaric AD (5–60 mm Hg). NMDA and AMPA receptor antagonists were injected in a cumulative fashion (1–100 μmol/kg, i.v.). After the conclusion of experiment, the abdomen was opened and receptive field was mapped by probing the serosa of the stomach. Thirty-two fibers were identified to AD. The receptive fields of 26 fibers were located in the posterior part of the antrum. All fibers exhibited spontaneous firing (mean: 7.00±0.97 impulses/s). Twenty fibers exhibited a rhythmic firing that was in phase with antral contractions, whereas 12 fibers exhibited non-rhythmic spontaneous firing unrelated to spontaneous antral contraction. Both groups of fibers exhibited a linear increase in responses to graded isovolumic or isobaric distensions. NMDA (memantine HCl and dizocilpine (MK-801)) and AMPA/kainate (6-cyano-7-nitroquinoxaline 2,3-dione; CNQX) receptor antagonists dose-dependently attenuated the mechanotransduction properties of these fibers to AD. However, competitive NMDA antagonist dl-2-amino-5 phosphopentanoic acid (AP-5) had no effect. The study documents that glutamate receptor antagonists can attenuate responses of gastric vagal sensory afferent fibers innervating the distal stomach, offering insight to potential pharmacological agents in the treatment of gastric disorders.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>15099685</pmid><doi>10.1016/j.neuroscience.2004.02.018</doi><tpages>13</tpages></addata></record>
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source ScienceDirect Journals
subjects Action Potentials - drug effects
Action Potentials - physiology
AMPA
Animals
antrum
Biological and medical sciences
Dilatation - instrumentation
Dilatation - methods
Dose-Response Relationship, Drug
Excitatory Amino Acid Antagonists - pharmacology
Fundamental and applied biological sciences. Psychology
Glutamic Acid - metabolism
Male
mechanoreceptors
Mechanoreceptors - drug effects
Mechanoreceptors - metabolism
Mechanotransduction, Cellular - drug effects
Mechanotransduction, Cellular - physiology
motility
Muscle Contraction - drug effects
Muscle Contraction - physiology
Muscle, Smooth - drug effects
Muscle, Smooth - physiology
Neurons, Afferent - drug effects
Neurons, Afferent - metabolism
NMDA
Physical Stimulation - instrumentation
Physical Stimulation - methods
Pyloric Antrum - drug effects
Pyloric Antrum - innervation
Pyloric Antrum - physiology
Rats
Rats, Long-Evans
Receptors, AMPA - antagonists & inhibitors
Receptors, AMPA - metabolism
Receptors, Glutamate - drug effects
Receptors, Glutamate - metabolism
Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors
Receptors, N-Methyl-D-Aspartate - metabolism
vagus
Vagus Nerve - drug effects
Vagus Nerve - physiology
Vertebrates: nervous system and sense organs
Visceral Afferents - drug effects
Visceral Afferents - metabolism
title Response properties of antral mechanosensitive afferent fibers and effects of ionotropic glutamate receptor antagonists
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