Evidence that distinct neural pathways mediate parasympathetic contractions and relaxations of guinea-pig trachealis
1. The guinea-pig trachea was isolated with its extrinsic innervation intact and pinned to the bottom of a water-jacketed dissecting dish filled with warmed, oxygenated Krebs solution. The trachea was not separated from the oesophagus. Isometric tension was measured in a segment of the rostral porti...
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description | 1. The guinea-pig trachea was isolated with its extrinsic innervation intact and pinned to the bottom of a water-jacketed
dissecting dish filled with warmed, oxygenated Krebs solution. The trachea was not separated from the oesophagus. Isometric
tension was measured in a segment of the rostral portion of the trachea. 2. Stimulation of the vagus nerves caudal to the
nodose ganglia elicited contractions of the trachealis that were blocked by the muscarinic receptor antagonist atropine. Following
addition of atropine and contraction of the trachealis with prostaglandin F2 alpha (PGF2 alpha), vagus nerve stimulation elicited
non-adrenergic, non-cholinergic relaxations. Both responses elicited by stimulation of the vagi were abolished by cutting
the recurrent laryngeal nerves and were considered parasympathetic in nature as they were sensitive to the autonomic ganglion
blockers trimetaphan and hexamethonium. 3. Experiments were designed in which ganglionic blockers were added to the buffer
bathing the entire preparation or, alternatively, added only to the buffer perfusing the tracheal lumen. When given equal
access to the trachea and oesophagus, hexamethonium was 56-fold more potent an inhibitor of vagally mediated relaxations of
the trachealis than vagally mediated contractions. Selective administration of hexamethonium to the buffer perfusing the tracheal
lumen did not decrease the potency of the ganglionic blocker versus vagally mediated contractions. By contrast, even at a
concentration of 1 mM, intratracheally administered hexamethonium failed to inhibit vagally mediated relaxations by 50%. Comparable
results were obtained using trimetaphan. 4. Consistent with previous observations, removing the portion of the oesophagus
contiguous with the region of the trachea at which isometric tension was measured abolished parasympathetic relaxations of
the trachealis. Oesophagus removal was without effect on parasympathetic nerve-induced contractions. Removing the dorsal half
of the oesophagus or the mucosa and submucosa of the oesophagus did not affect the parasympathetic relaxant innervation. 5.
The compound action potential of guinea-pig recurrent laryngeal nerves evoked by vagus nerve stimulation consisted of three
distinct peaks representing populations of axons with fast, intermediate and slow conduction velocities. The voltage-response
characteristics of vagally mediated contractions were identical to those of the compound action potential peak representing
f |
doi_str_mv | 10.1113/jphysiol.1993.sp019889 |
format | Article |
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dissecting dish filled with warmed, oxygenated Krebs solution. The trachea was not separated from the oesophagus. Isometric
tension was measured in a segment of the rostral portion of the trachea. 2. Stimulation of the vagus nerves caudal to the
nodose ganglia elicited contractions of the trachealis that were blocked by the muscarinic receptor antagonist atropine. Following
addition of atropine and contraction of the trachealis with prostaglandin F2 alpha (PGF2 alpha), vagus nerve stimulation elicited
non-adrenergic, non-cholinergic relaxations. Both responses elicited by stimulation of the vagi were abolished by cutting
the recurrent laryngeal nerves and were considered parasympathetic in nature as they were sensitive to the autonomic ganglion
blockers trimetaphan and hexamethonium. 3. Experiments were designed in which ganglionic blockers were added to the buffer
bathing the entire preparation or, alternatively, added only to the buffer perfusing the tracheal lumen. When given equal
access to the trachea and oesophagus, hexamethonium was 56-fold more potent an inhibitor of vagally mediated relaxations of
the trachealis than vagally mediated contractions. Selective administration of hexamethonium to the buffer perfusing the tracheal
lumen did not decrease the potency of the ganglionic blocker versus vagally mediated contractions. By contrast, even at a
concentration of 1 mM, intratracheally administered hexamethonium failed to inhibit vagally mediated relaxations by 50%. Comparable
results were obtained using trimetaphan. 4. Consistent with previous observations, removing the portion of the oesophagus
contiguous with the region of the trachea at which isometric tension was measured abolished parasympathetic relaxations of
the trachealis. Oesophagus removal was without effect on parasympathetic nerve-induced contractions. Removing the dorsal half
of the oesophagus or the mucosa and submucosa of the oesophagus did not affect the parasympathetic relaxant innervation. 5.
The compound action potential of guinea-pig recurrent laryngeal nerves evoked by vagus nerve stimulation consisted of three
distinct peaks representing populations of axons with fast, intermediate and slow conduction velocities. The voltage-response
characteristics of vagally mediated contractions were identical to those of the compound action potential peak representing
fibres with intermediate (10 m/s) conduction velocities. By contrast, the voltage-response characteristics of the vagally
mediated relaxations were best correlated with the compound action potential peak representing fibres with slow (0.4-3 m/s)
conduction velocities.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/jphysiol.1993.sp019889</identifier><identifier>PMID: 7907144</identifier><identifier>CODEN: JPHYA7</identifier><language>eng</language><publisher>Oxford: The Physiological Society</publisher><subject>Action Potentials - physiology ; Animals ; Atropine - pharmacology ; Biological and medical sciences ; Cardiorespiratory control. Arterial mecano- and chemoreceptor ; Dinoprost - pharmacology ; Electric Stimulation ; Esophagus - innervation ; Esophagus - physiology ; Fundamental and applied biological sciences. Psychology ; Ganglia, Parasympathetic - drug effects ; Ganglia, Parasympathetic - physiology ; Guinea Pigs ; Hexamethonium ; Hexamethonium Compounds - pharmacology ; In Vitro Techniques ; Male ; Muscle Contraction - drug effects ; Muscle Contraction - physiology ; Muscle Relaxation - drug effects ; Muscle Relaxation - physiology ; Muscle, Smooth - drug effects ; Muscle, Smooth - innervation ; Muscle, Smooth - physiology ; Neural Pathways - drug effects ; Neural Pathways - physiology ; Parasympathetic Nervous System - drug effects ; Parasympathetic Nervous System - physiology ; Recurrent Laryngeal Nerve - physiology ; Trachea - drug effects ; Trachea - innervation ; Trachea - physiology ; Trimethaphan - pharmacology ; Vagus Nerve - physiology ; Vertebrates: respiratory system</subject><ispartof>The Journal of physiology, 1993-11, Vol.471 (1), p.25-40</ispartof><rights>1993 The Physiological Society</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5605-496b536dd7f736a8ea532cf8a1a20c8b1efb40adcae7dd96005ffca9e6f491223</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1143950/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1143950/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,27924,27925,45574,45575,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3792426$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7907144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Canning, B J</creatorcontrib><creatorcontrib>Undem, B J</creatorcontrib><title>Evidence that distinct neural pathways mediate parasympathetic contractions and relaxations of guinea-pig trachealis</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>1. The guinea-pig trachea was isolated with its extrinsic innervation intact and pinned to the bottom of a water-jacketed
dissecting dish filled with warmed, oxygenated Krebs solution. The trachea was not separated from the oesophagus. Isometric
tension was measured in a segment of the rostral portion of the trachea. 2. Stimulation of the vagus nerves caudal to the
nodose ganglia elicited contractions of the trachealis that were blocked by the muscarinic receptor antagonist atropine. Following
addition of atropine and contraction of the trachealis with prostaglandin F2 alpha (PGF2 alpha), vagus nerve stimulation elicited
non-adrenergic, non-cholinergic relaxations. Both responses elicited by stimulation of the vagi were abolished by cutting
the recurrent laryngeal nerves and were considered parasympathetic in nature as they were sensitive to the autonomic ganglion
blockers trimetaphan and hexamethonium. 3. Experiments were designed in which ganglionic blockers were added to the buffer
bathing the entire preparation or, alternatively, added only to the buffer perfusing the tracheal lumen. When given equal
access to the trachea and oesophagus, hexamethonium was 56-fold more potent an inhibitor of vagally mediated relaxations of
the trachealis than vagally mediated contractions. Selective administration of hexamethonium to the buffer perfusing the tracheal
lumen did not decrease the potency of the ganglionic blocker versus vagally mediated contractions. By contrast, even at a
concentration of 1 mM, intratracheally administered hexamethonium failed to inhibit vagally mediated relaxations by 50%. Comparable
results were obtained using trimetaphan. 4. Consistent with previous observations, removing the portion of the oesophagus
contiguous with the region of the trachea at which isometric tension was measured abolished parasympathetic relaxations of
the trachealis. Oesophagus removal was without effect on parasympathetic nerve-induced contractions. Removing the dorsal half
of the oesophagus or the mucosa and submucosa of the oesophagus did not affect the parasympathetic relaxant innervation. 5.
The compound action potential of guinea-pig recurrent laryngeal nerves evoked by vagus nerve stimulation consisted of three
distinct peaks representing populations of axons with fast, intermediate and slow conduction velocities. The voltage-response
characteristics of vagally mediated contractions were identical to those of the compound action potential peak representing
fibres with intermediate (10 m/s) conduction velocities. By contrast, the voltage-response characteristics of the vagally
mediated relaxations were best correlated with the compound action potential peak representing fibres with slow (0.4-3 m/s)
conduction velocities.</description><subject>Action Potentials - physiology</subject><subject>Animals</subject><subject>Atropine - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cardiorespiratory control. Arterial mecano- and chemoreceptor</subject><subject>Dinoprost - pharmacology</subject><subject>Electric Stimulation</subject><subject>Esophagus - innervation</subject><subject>Esophagus - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ganglia, Parasympathetic - drug effects</subject><subject>Ganglia, Parasympathetic - physiology</subject><subject>Guinea Pigs</subject><subject>Hexamethonium</subject><subject>Hexamethonium Compounds - pharmacology</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle Relaxation - drug effects</subject><subject>Muscle Relaxation - physiology</subject><subject>Muscle, Smooth - drug effects</subject><subject>Muscle, Smooth - innervation</subject><subject>Muscle, Smooth - physiology</subject><subject>Neural Pathways - drug effects</subject><subject>Neural Pathways - physiology</subject><subject>Parasympathetic Nervous System - drug effects</subject><subject>Parasympathetic Nervous System - physiology</subject><subject>Recurrent Laryngeal Nerve - physiology</subject><subject>Trachea - drug effects</subject><subject>Trachea - innervation</subject><subject>Trachea - physiology</subject><subject>Trimethaphan - pharmacology</subject><subject>Vagus Nerve - physiology</subject><subject>Vertebrates: respiratory system</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1v1DAQhiMEKkvhJ4ByQBWXLJ44seMLUlWVL1WCQzlbs85k48qbBNvbJf-ehGwXuCBOlud95vNNklfA1gDA394N7Rhs79agFF-HgYGqKvUoWUEhVCal4o-TFWN5nnFZwtPkWQh3jAFnSp0lZ1IxCUWxSuL1va2pM5TGFmNa2xBtZ2La0d6jSweM7QHHkO6othhpCngM426OU7QmNX0XPZpo-y6k2NWpJ4c_cPn3Tbrd244wG-w2nbmW0NnwPHnSoAv04vieJ9_eX99efcxuvnz4dHV5k5lSsDIrlNiUXNS1bCQXWBGWPDdNhYA5M9UGqNkUDGuDJOtaCcbKpjGoSDSFgjzn58m7pe6w30wLGJpndXrwdod-1D1a_bfS2VZv-3sNUHBVsqnAxbGA77_vKUS9s8GQc9hRvw9aipyXUlQT-OafIMiSF5WAXEyoWFDj-xA8Nad5gOnZWv1grZ6t1Q_WTokv_9zmlHb0ctJfH3UMBl3jsTM2nDAuVV786n-5YAfraPzP5vr289c5UEiAvPx9l9Zu24P1pJes0BtLcdQTpkFP4E95_Na8</recordid><startdate>19931101</startdate><enddate>19931101</enddate><creator>Canning, B J</creator><creator>Undem, B J</creator><general>The Physiological Society</general><general>Blackwell</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><scope>5PM</scope></search><sort><creationdate>19931101</creationdate><title>Evidence that distinct neural pathways mediate parasympathetic contractions and relaxations of guinea-pig trachealis</title><author>Canning, B J ; Undem, B J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5605-496b536dd7f736a8ea532cf8a1a20c8b1efb40adcae7dd96005ffca9e6f491223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Action Potentials - physiology</topic><topic>Animals</topic><topic>Atropine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cardiorespiratory control. Arterial mecano- and chemoreceptor</topic><topic>Dinoprost - pharmacology</topic><topic>Electric Stimulation</topic><topic>Esophagus - innervation</topic><topic>Esophagus - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglia, Parasympathetic - drug effects</topic><topic>Ganglia, Parasympathetic - physiology</topic><topic>Guinea Pigs</topic><topic>Hexamethonium</topic><topic>Hexamethonium Compounds - pharmacology</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle Relaxation - drug effects</topic><topic>Muscle Relaxation - physiology</topic><topic>Muscle, Smooth - drug effects</topic><topic>Muscle, Smooth - innervation</topic><topic>Muscle, Smooth - physiology</topic><topic>Neural Pathways - drug effects</topic><topic>Neural Pathways - physiology</topic><topic>Parasympathetic Nervous System - drug effects</topic><topic>Parasympathetic Nervous System - physiology</topic><topic>Recurrent Laryngeal Nerve - physiology</topic><topic>Trachea - drug effects</topic><topic>Trachea - innervation</topic><topic>Trachea - physiology</topic><topic>Trimethaphan - pharmacology</topic><topic>Vagus Nerve - physiology</topic><topic>Vertebrates: respiratory system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Canning, B J</creatorcontrib><creatorcontrib>Undem, B J</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Canning, B J</au><au>Undem, B J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence that distinct neural pathways mediate parasympathetic contractions and relaxations of guinea-pig trachealis</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>1993-11-01</date><risdate>1993</risdate><volume>471</volume><issue>1</issue><spage>25</spage><epage>40</epage><pages>25-40</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><coden>JPHYA7</coden><abstract>1. The guinea-pig trachea was isolated with its extrinsic innervation intact and pinned to the bottom of a water-jacketed
dissecting dish filled with warmed, oxygenated Krebs solution. The trachea was not separated from the oesophagus. Isometric
tension was measured in a segment of the rostral portion of the trachea. 2. Stimulation of the vagus nerves caudal to the
nodose ganglia elicited contractions of the trachealis that were blocked by the muscarinic receptor antagonist atropine. Following
addition of atropine and contraction of the trachealis with prostaglandin F2 alpha (PGF2 alpha), vagus nerve stimulation elicited
non-adrenergic, non-cholinergic relaxations. Both responses elicited by stimulation of the vagi were abolished by cutting
the recurrent laryngeal nerves and were considered parasympathetic in nature as they were sensitive to the autonomic ganglion
blockers trimetaphan and hexamethonium. 3. Experiments were designed in which ganglionic blockers were added to the buffer
bathing the entire preparation or, alternatively, added only to the buffer perfusing the tracheal lumen. When given equal
access to the trachea and oesophagus, hexamethonium was 56-fold more potent an inhibitor of vagally mediated relaxations of
the trachealis than vagally mediated contractions. Selective administration of hexamethonium to the buffer perfusing the tracheal
lumen did not decrease the potency of the ganglionic blocker versus vagally mediated contractions. By contrast, even at a
concentration of 1 mM, intratracheally administered hexamethonium failed to inhibit vagally mediated relaxations by 50%. Comparable
results were obtained using trimetaphan. 4. Consistent with previous observations, removing the portion of the oesophagus
contiguous with the region of the trachea at which isometric tension was measured abolished parasympathetic relaxations of
the trachealis. Oesophagus removal was without effect on parasympathetic nerve-induced contractions. Removing the dorsal half
of the oesophagus or the mucosa and submucosa of the oesophagus did not affect the parasympathetic relaxant innervation. 5.
The compound action potential of guinea-pig recurrent laryngeal nerves evoked by vagus nerve stimulation consisted of three
distinct peaks representing populations of axons with fast, intermediate and slow conduction velocities. The voltage-response
characteristics of vagally mediated contractions were identical to those of the compound action potential peak representing
fibres with intermediate (10 m/s) conduction velocities. By contrast, the voltage-response characteristics of the vagally
mediated relaxations were best correlated with the compound action potential peak representing fibres with slow (0.4-3 m/s)
conduction velocities.</abstract><cop>Oxford</cop><pub>The Physiological Society</pub><pmid>7907144</pmid><doi>10.1113/jphysiol.1993.sp019889</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Access via Wiley Online Library; IngentaConnect Free/Open Access Journals; PubMed Central; Alma/SFX Local Collection |
subjects | Action Potentials - physiology Animals Atropine - pharmacology Biological and medical sciences Cardiorespiratory control. Arterial mecano- and chemoreceptor Dinoprost - pharmacology Electric Stimulation Esophagus - innervation Esophagus - physiology Fundamental and applied biological sciences. Psychology Ganglia, Parasympathetic - drug effects Ganglia, Parasympathetic - physiology Guinea Pigs Hexamethonium Hexamethonium Compounds - pharmacology In Vitro Techniques Male Muscle Contraction - drug effects Muscle Contraction - physiology Muscle Relaxation - drug effects Muscle Relaxation - physiology Muscle, Smooth - drug effects Muscle, Smooth - innervation Muscle, Smooth - physiology Neural Pathways - drug effects Neural Pathways - physiology Parasympathetic Nervous System - drug effects Parasympathetic Nervous System - physiology Recurrent Laryngeal Nerve - physiology Trachea - drug effects Trachea - innervation Trachea - physiology Trimethaphan - pharmacology Vagus Nerve - physiology Vertebrates: respiratory system |
title | Evidence that distinct neural pathways mediate parasympathetic contractions and relaxations of guinea-pig trachealis |
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