Stress-induced changes in the function of the parasympathetic nervous system are mimicked by blocking GABA in the cns of the cat

The purpose of this study was to determine the effect of blockade of receptors for γ-aminobutyric acid (GABA) in the forebrain, on vagal activity to the stomach and heart. This was done by injecting bicuculline (50 μg) into the lateral ventricle of the brain and restricting the drug to the forebrain...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Neuropharmacology 1987-02, Vol.26 (2), p.155-160
Hauptverfasser: Pagani, F.D., DiMicco, J.A., Hamilton, B.L., Souza, J.D., Schmidt, B., Gillis, R.A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 160
container_issue 2
container_start_page 155
container_title Neuropharmacology
container_volume 26
creator Pagani, F.D.
DiMicco, J.A.
Hamilton, B.L.
Souza, J.D.
Schmidt, B.
Gillis, R.A.
description The purpose of this study was to determine the effect of blockade of receptors for γ-aminobutyric acid (GABA) in the forebrain, on vagal activity to the stomach and heart. This was done by injecting bicuculline (50 μg) into the lateral ventricle of the brain and restricting the drug to the forebrain ventricles by cannulating the cerebral aqueduct. Studies were performed in chloraloseanesthetized cats and gastric motility was monitored using extraluminal force transducers, sutured to the antrum and pylorus. Cardiac vagal activity was determined by noting the sinus bradycardia that developed from activation of the baroreceptor reflex induced by phenylephrine. Administration of bicuculline into the lateral ventricle of 7 animals produced increases in the minute motility index of 5.3 ± 0.8 (antrum) and 13.9 ± 2.1 (pylorus). This was associated with inhibition of baroreceptor-induced vagal bradycardia (i.e. −38 ± 6.4 beats/min before bicuculline and −7.7 ± 5.7 beats/min after bicuculline). These data indicate that a GABAergic mechanism in the forebrain may be important for controlling vagal outflow to both the stomach and the heart.
doi_str_mv 10.1016/0028-3908(87)90203-6
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_77564112</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0028390887902036</els_id><sourcerecordid>77564112</sourcerecordid><originalsourceid>FETCH-LOGICAL-c432t-4be5191d50e86e5d83b9818ca899c56d1a785a1e18415cf0f38579170d0f3f763</originalsourceid><addsrcrecordid>eNp9kcGOFCEQhonRrOPqG2jCwRg9tMIADVxMxo2uJpt4UM-Epqt3cbvpkaI3mZuPLrMzO0dPUKmPP1UfhLzk7D1nvP3A2No0wjLz1uh3lq2ZaNpHZMWNFo1mrXxMVifkKXmG-JsxJg03Z-RMMKEk5yvy90fJgNjE1C8BehpufLoGpDHRcgN0WFIocU50Hu7rrc8ed9PW16LEQBPku3lBijssMFGfgU5xiuG2RnU72o1zuI3pml5uPm0eMkPCh7jgy3PyZPAjwovjeU5-ffn88-Jrc_X98tvF5qoJUqxLIztQ3PJeMTAtqN6IztZVgjfWBtX23GujPAduJFdhYIMwSluuWV-vg27FOXlzyN3m-c8CWNwUMcA4-gR1A6e1aquRdQXlAQx5RswwuG2Ok887x5nbi3d7q25v1Rnt7sW7ff6rY_7STdCfHh1N1_7rY99j8OOQfQoRT5iWlktjK_bxgEF1cRchOwwRUv2amCEU18_x_3P8A8U_nu0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>77564112</pqid></control><display><type>article</type><title>Stress-induced changes in the function of the parasympathetic nervous system are mimicked by blocking GABA in the cns of the cat</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Pagani, F.D. ; DiMicco, J.A. ; Hamilton, B.L. ; Souza, J.D. ; Schmidt, B. ; Gillis, R.A.</creator><creatorcontrib>Pagani, F.D. ; DiMicco, J.A. ; Hamilton, B.L. ; Souza, J.D. ; Schmidt, B. ; Gillis, R.A.</creatorcontrib><description>The purpose of this study was to determine the effect of blockade of receptors for γ-aminobutyric acid (GABA) in the forebrain, on vagal activity to the stomach and heart. This was done by injecting bicuculline (50 μg) into the lateral ventricle of the brain and restricting the drug to the forebrain ventricles by cannulating the cerebral aqueduct. Studies were performed in chloraloseanesthetized cats and gastric motility was monitored using extraluminal force transducers, sutured to the antrum and pylorus. Cardiac vagal activity was determined by noting the sinus bradycardia that developed from activation of the baroreceptor reflex induced by phenylephrine. Administration of bicuculline into the lateral ventricle of 7 animals produced increases in the minute motility index of 5.3 ± 0.8 (antrum) and 13.9 ± 2.1 (pylorus). This was associated with inhibition of baroreceptor-induced vagal bradycardia (i.e. −38 ± 6.4 beats/min before bicuculline and −7.7 ± 5.7 beats/min after bicuculline). These data indicate that a GABAergic mechanism in the forebrain may be important for controlling vagal outflow to both the stomach and the heart.</description><identifier>ISSN: 0028-3908</identifier><identifier>EISSN: 1873-7064</identifier><identifier>DOI: 10.1016/0028-3908(87)90203-6</identifier><identifier>PMID: 3035411</identifier><identifier>CODEN: NEPHBW</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; bicuculline ; Bicuculline - administration &amp; dosage ; Bicuculline - pharmacology ; Biological and medical sciences ; Cats ; Central Nervous System - drug effects ; CNS control of G.I. function ; GABA Antagonists ; gastric motility ; heart rate ; Injections, Intraventricular ; Medical sciences ; Miscellaneous ; muscimol ; Neuropharmacology ; Neurotransmitters. Neurotransmission. Receptors ; Parasympathetic Nervous System - drug effects ; Parasympathetic Nervous System - physiology ; Pharmacology. Drug treatments ; picrotoxin ; Receptors, GABA-A - drug effects ; vagal tone</subject><ispartof>Neuropharmacology, 1987-02, Vol.26 (2), p.155-160</ispartof><rights>1987</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-4be5191d50e86e5d83b9818ca899c56d1a785a1e18415cf0f38579170d0f3f763</citedby><cites>FETCH-LOGICAL-c432t-4be5191d50e86e5d83b9818ca899c56d1a785a1e18415cf0f38579170d0f3f763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0028-3908(87)90203-6$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=7491489$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3035411$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pagani, F.D.</creatorcontrib><creatorcontrib>DiMicco, J.A.</creatorcontrib><creatorcontrib>Hamilton, B.L.</creatorcontrib><creatorcontrib>Souza, J.D.</creatorcontrib><creatorcontrib>Schmidt, B.</creatorcontrib><creatorcontrib>Gillis, R.A.</creatorcontrib><title>Stress-induced changes in the function of the parasympathetic nervous system are mimicked by blocking GABA in the cns of the cat</title><title>Neuropharmacology</title><addtitle>Neuropharmacology</addtitle><description>The purpose of this study was to determine the effect of blockade of receptors for γ-aminobutyric acid (GABA) in the forebrain, on vagal activity to the stomach and heart. This was done by injecting bicuculline (50 μg) into the lateral ventricle of the brain and restricting the drug to the forebrain ventricles by cannulating the cerebral aqueduct. Studies were performed in chloraloseanesthetized cats and gastric motility was monitored using extraluminal force transducers, sutured to the antrum and pylorus. Cardiac vagal activity was determined by noting the sinus bradycardia that developed from activation of the baroreceptor reflex induced by phenylephrine. Administration of bicuculline into the lateral ventricle of 7 animals produced increases in the minute motility index of 5.3 ± 0.8 (antrum) and 13.9 ± 2.1 (pylorus). This was associated with inhibition of baroreceptor-induced vagal bradycardia (i.e. −38 ± 6.4 beats/min before bicuculline and −7.7 ± 5.7 beats/min after bicuculline). These data indicate that a GABAergic mechanism in the forebrain may be important for controlling vagal outflow to both the stomach and the heart.</description><subject>Animals</subject><subject>bicuculline</subject><subject>Bicuculline - administration &amp; dosage</subject><subject>Bicuculline - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cats</subject><subject>Central Nervous System - drug effects</subject><subject>CNS control of G.I. function</subject><subject>GABA Antagonists</subject><subject>gastric motility</subject><subject>heart rate</subject><subject>Injections, Intraventricular</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>muscimol</subject><subject>Neuropharmacology</subject><subject>Neurotransmitters. Neurotransmission. Receptors</subject><subject>Parasympathetic Nervous System - drug effects</subject><subject>Parasympathetic Nervous System - physiology</subject><subject>Pharmacology. Drug treatments</subject><subject>picrotoxin</subject><subject>Receptors, GABA-A - drug effects</subject><subject>vagal tone</subject><issn>0028-3908</issn><issn>1873-7064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcGOFCEQhonRrOPqG2jCwRg9tMIADVxMxo2uJpt4UM-Epqt3cbvpkaI3mZuPLrMzO0dPUKmPP1UfhLzk7D1nvP3A2No0wjLz1uh3lq2ZaNpHZMWNFo1mrXxMVifkKXmG-JsxJg03Z-RMMKEk5yvy90fJgNjE1C8BehpufLoGpDHRcgN0WFIocU50Hu7rrc8ed9PW16LEQBPku3lBijssMFGfgU5xiuG2RnU72o1zuI3pml5uPm0eMkPCh7jgy3PyZPAjwovjeU5-ffn88-Jrc_X98tvF5qoJUqxLIztQ3PJeMTAtqN6IztZVgjfWBtX23GujPAduJFdhYIMwSluuWV-vg27FOXlzyN3m-c8CWNwUMcA4-gR1A6e1aquRdQXlAQx5RswwuG2Ok887x5nbi3d7q25v1Rnt7sW7ff6rY_7STdCfHh1N1_7rY99j8OOQfQoRT5iWlktjK_bxgEF1cRchOwwRUv2amCEU18_x_3P8A8U_nu0</recordid><startdate>19870201</startdate><enddate>19870201</enddate><creator>Pagani, F.D.</creator><creator>DiMicco, J.A.</creator><creator>Hamilton, B.L.</creator><creator>Souza, J.D.</creator><creator>Schmidt, B.</creator><creator>Gillis, R.A.</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>7X8</scope></search><sort><creationdate>19870201</creationdate><title>Stress-induced changes in the function of the parasympathetic nervous system are mimicked by blocking GABA in the cns of the cat</title><author>Pagani, F.D. ; DiMicco, J.A. ; Hamilton, B.L. ; Souza, J.D. ; Schmidt, B. ; Gillis, R.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-4be5191d50e86e5d83b9818ca899c56d1a785a1e18415cf0f38579170d0f3f763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Animals</topic><topic>bicuculline</topic><topic>Bicuculline - administration &amp; dosage</topic><topic>Bicuculline - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cats</topic><topic>Central Nervous System - drug effects</topic><topic>CNS control of G.I. function</topic><topic>GABA Antagonists</topic><topic>gastric motility</topic><topic>heart rate</topic><topic>Injections, Intraventricular</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>muscimol</topic><topic>Neuropharmacology</topic><topic>Neurotransmitters. Neurotransmission. Receptors</topic><topic>Parasympathetic Nervous System - drug effects</topic><topic>Parasympathetic Nervous System - physiology</topic><topic>Pharmacology. Drug treatments</topic><topic>picrotoxin</topic><topic>Receptors, GABA-A - drug effects</topic><topic>vagal tone</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pagani, F.D.</creatorcontrib><creatorcontrib>DiMicco, J.A.</creatorcontrib><creatorcontrib>Hamilton, B.L.</creatorcontrib><creatorcontrib>Souza, J.D.</creatorcontrib><creatorcontrib>Schmidt, B.</creatorcontrib><creatorcontrib>Gillis, R.A.</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>MEDLINE - Academic</collection><jtitle>Neuropharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pagani, F.D.</au><au>DiMicco, J.A.</au><au>Hamilton, B.L.</au><au>Souza, J.D.</au><au>Schmidt, B.</au><au>Gillis, R.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stress-induced changes in the function of the parasympathetic nervous system are mimicked by blocking GABA in the cns of the cat</atitle><jtitle>Neuropharmacology</jtitle><addtitle>Neuropharmacology</addtitle><date>1987-02-01</date><risdate>1987</risdate><volume>26</volume><issue>2</issue><spage>155</spage><epage>160</epage><pages>155-160</pages><issn>0028-3908</issn><eissn>1873-7064</eissn><coden>NEPHBW</coden><abstract>The purpose of this study was to determine the effect of blockade of receptors for γ-aminobutyric acid (GABA) in the forebrain, on vagal activity to the stomach and heart. This was done by injecting bicuculline (50 μg) into the lateral ventricle of the brain and restricting the drug to the forebrain ventricles by cannulating the cerebral aqueduct. Studies were performed in chloraloseanesthetized cats and gastric motility was monitored using extraluminal force transducers, sutured to the antrum and pylorus. Cardiac vagal activity was determined by noting the sinus bradycardia that developed from activation of the baroreceptor reflex induced by phenylephrine. Administration of bicuculline into the lateral ventricle of 7 animals produced increases in the minute motility index of 5.3 ± 0.8 (antrum) and 13.9 ± 2.1 (pylorus). This was associated with inhibition of baroreceptor-induced vagal bradycardia (i.e. −38 ± 6.4 beats/min before bicuculline and −7.7 ± 5.7 beats/min after bicuculline). These data indicate that a GABAergic mechanism in the forebrain may be important for controlling vagal outflow to both the stomach and the heart.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>3035411</pmid><doi>10.1016/0028-3908(87)90203-6</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0028-3908
ispartof Neuropharmacology, 1987-02, Vol.26 (2), p.155-160
issn 0028-3908
1873-7064
language eng
recordid cdi_proquest_miscellaneous_77564112
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
bicuculline
Bicuculline - administration & dosage
Bicuculline - pharmacology
Biological and medical sciences
Cats
Central Nervous System - drug effects
CNS control of G.I. function
GABA Antagonists
gastric motility
heart rate
Injections, Intraventricular
Medical sciences
Miscellaneous
muscimol
Neuropharmacology
Neurotransmitters. Neurotransmission. Receptors
Parasympathetic Nervous System - drug effects
Parasympathetic Nervous System - physiology
Pharmacology. Drug treatments
picrotoxin
Receptors, GABA-A - drug effects
vagal tone
title Stress-induced changes in the function of the parasympathetic nervous system are mimicked by blocking GABA in the cns of the cat
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T17%3A52%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Stress-induced%20changes%20in%20the%20function%20of%20the%20parasympathetic%20nervous%20system%20are%20mimicked%20by%20blocking%20GABA%20in%20the%20cns%20of%20the%20cat&rft.jtitle=Neuropharmacology&rft.au=Pagani,%20F.D.&rft.date=1987-02-01&rft.volume=26&rft.issue=2&rft.spage=155&rft.epage=160&rft.pages=155-160&rft.issn=0028-3908&rft.eissn=1873-7064&rft.coden=NEPHBW&rft_id=info:doi/10.1016/0028-3908(87)90203-6&rft_dat=%3Cproquest_cross%3E77564112%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=77564112&rft_id=info:pmid/3035411&rft_els_id=0028390887902036&rfr_iscdi=true