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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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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. |
doi_str_mv | 10.1016/j.neuroscience.2004.02.018 |
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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
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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.</description><subject>Action Potentials - drug effects</subject><subject>Action Potentials - physiology</subject><subject>AMPA</subject><subject>Animals</subject><subject>antrum</subject><subject>Biological and medical sciences</subject><subject>Dilatation - instrumentation</subject><subject>Dilatation - methods</subject><subject>Dose-Response Relationship, Drug</subject><subject>Excitatory Amino Acid Antagonists - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glutamic Acid - metabolism</subject><subject>Male</subject><subject>mechanoreceptors</subject><subject>Mechanoreceptors - drug effects</subject><subject>Mechanoreceptors - metabolism</subject><subject>Mechanotransduction, Cellular - drug effects</subject><subject>Mechanotransduction, Cellular - physiology</subject><subject>motility</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle, Smooth - drug effects</subject><subject>Muscle, Smooth - physiology</subject><subject>Neurons, Afferent - drug effects</subject><subject>Neurons, Afferent - metabolism</subject><subject>NMDA</subject><subject>Physical Stimulation - instrumentation</subject><subject>Physical Stimulation - methods</subject><subject>Pyloric Antrum - drug effects</subject><subject>Pyloric Antrum - innervation</subject><subject>Pyloric Antrum - physiology</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Receptors, AMPA - antagonists & inhibitors</subject><subject>Receptors, AMPA - metabolism</subject><subject>Receptors, Glutamate - drug effects</subject><subject>Receptors, Glutamate - metabolism</subject><subject>Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors</subject><subject>Receptors, N-Methyl-D-Aspartate - metabolism</subject><subject>vagus</subject><subject>Vagus Nerve - drug effects</subject><subject>Vagus Nerve - physiology</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Visceral Afferents - drug effects</subject><subject>Visceral Afferents - metabolism</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqNkVuL1TAUhYMoznH0L0gR9K01aZIm9U1mvMGAIPoc0nR3zKFNanY64r83x1Nw3jQvG8K31r4sQl4w2jDKutfHJsCWIjoPwUHTUioa2jaU6QfkwLTitZJCPCQHymlXC9m2F-QJ4pGWJwV_TC6YpH3faXkgP78ArjEgVGuKK6TsAas4VTbkZOdqAffdhogQ0Gd_B5WdJkgQcjX5ARIWbqyg_Ln8R-ZjiLkYeVfdzlu2i81QJXCw5phOpvY2Bo8Zn5JHk50Rnu31knx7_-7r1cf65vOHT1dvb2onuMo141I46JkbqWaDVs52QlA7OKUliJYPHW-5VIMQPe-oFsJa1oNWHbTd6PqRX5JXZ9-y3o8NMJvFo4N5tgHihkYxLXuhxT9BppTkWrICvjmDrkSACSazJr_Y9Mswak75mKO5n4855WNoa0o-Rfx877INC4x_pXsgBXi5Axadnadkg_N4jysDl_UKd33moBzvzkMye7vRl3NnM0b_P_P8BqT8uAw</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Sengupta, J.N</creator><creator>Petersen, J</creator><creator>Peles, S</creator><creator>Shaker, R</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>2004</creationdate><title>Response properties of antral mechanosensitive afferent fibers and effects of ionotropic glutamate receptor antagonists</title><author>Sengupta, J.N ; Petersen, J ; Peles, S ; Shaker, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-1354ce91cd081b87ca6440abc785e423b632357b449360844aa19e876e26dc9d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Action Potentials - drug effects</topic><topic>Action Potentials - physiology</topic><topic>AMPA</topic><topic>Animals</topic><topic>antrum</topic><topic>Biological and medical sciences</topic><topic>Dilatation - instrumentation</topic><topic>Dilatation - methods</topic><topic>Dose-Response Relationship, Drug</topic><topic>Excitatory Amino Acid Antagonists - pharmacology</topic><topic>Fundamental and applied biological sciences. 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 & 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 & 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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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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