Pacemaker shift in the gastric antrum of guinea-pigs produced by excitatory vagal stimulation involves intramuscular interstitial cells
Intracellular recordings were made from isolated bundles of the circular muscle layer of guinea-pig gastric antrum and the responses produced by stimulating intrinsic nerve fibres were examined. After abolishing the effects of stimulating inhibitory nerve terminals with apamin and l -nitroarginine (...
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description | Intracellular recordings were made from isolated bundles of the circular muscle layer of guinea-pig gastric antrum and the
responses produced by stimulating intrinsic nerve fibres were examined. After abolishing the effects of stimulating inhibitory
nerve terminals with apamin and l -nitroarginine (NOLA), transmural nerve stimulation often evoked a small amplitude excitatory junction potential (EJP) and
invariably evoked a regenerative potential. Neurally evoked regenerative potentials had similar properties to those evoked
in the same bundle by direct stimulation. EJPs and neurally evoked regenerative potentials were abolished by hyoscine suggesting
that both resulted from the release of acetylcholine and activation of muscarinic receptors. Neurally evoked regenerative
potentials, but not EJPs, were abolished by membrane hyperpolarization, caffeine and chloride channel blockers. In the intact
antrum, excitatory vagal nerve stimulation increased the frequency of slow waves. Simultaneous intracellular recordings of
pacemaker potentials from myenteric interstitial cells (ICC MY ) and slow waves showed that the onset of each pacemaker potential normally preceded the onset of each slow wave but vagal
stimulation caused the onset of each slow wave to precede each pacemaker potential. Together the observations suggest that
during vagal stimulation there is a change in the origin of pacemaker activity with slow waves being initiated by intramuscular
interstitial cells (ICC IM ) rather than by ICC MY . |
doi_str_mv | 10.1113/jphysiol.2002.018614 |
format | Article |
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responses produced by stimulating intrinsic nerve fibres were examined. After abolishing the effects of stimulating inhibitory
nerve terminals with apamin and l -nitroarginine (NOLA), transmural nerve stimulation often evoked a small amplitude excitatory junction potential (EJP) and
invariably evoked a regenerative potential. Neurally evoked regenerative potentials had similar properties to those evoked
in the same bundle by direct stimulation. EJPs and neurally evoked regenerative potentials were abolished by hyoscine suggesting
that both resulted from the release of acetylcholine and activation of muscarinic receptors. Neurally evoked regenerative
potentials, but not EJPs, were abolished by membrane hyperpolarization, caffeine and chloride channel blockers. In the intact
antrum, excitatory vagal nerve stimulation increased the frequency of slow waves. Simultaneous intracellular recordings of
pacemaker potentials from myenteric interstitial cells (ICC MY ) and slow waves showed that the onset of each pacemaker potential normally preceded the onset of each slow wave but vagal
stimulation caused the onset of each slow wave to precede each pacemaker potential. Together the observations suggest that
during vagal stimulation there is a change in the origin of pacemaker activity with slow waves being initiated by intramuscular
interstitial cells (ICC IM ) rather than by ICC MY .</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/jphysiol.2002.018614</identifier><identifier>PMID: 12068050</identifier><language>eng</language><publisher>Oxford, UK: The Physiological Society</publisher><subject>4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid - pharmacology ; Animals ; Apamin - pharmacology ; Biological Clocks - physiology ; Boron Compounds - pharmacology ; Electric Stimulation ; Evoked Potentials - drug effects ; Evoked Potentials - physiology ; Excitatory Postsynaptic Potentials - drug effects ; Excitatory Postsynaptic Potentials - physiology ; Female ; Guinea Pigs ; In Vitro Techniques ; Male ; Membrane Potentials - physiology ; Muscarinic Antagonists - pharmacology ; Muscle, Smooth - cytology ; Muscle, Smooth - innervation ; Muscle, Smooth - physiology ; Nerve Endings - physiology ; Nitroarginine - pharmacology ; Original ; Pyloric Antrum - innervation ; Pyloric Antrum - physiology ; Scopolamine - pharmacology ; Stomach - cytology ; Stomach - innervation ; Stomach - physiology ; Vagus Nerve - physiology</subject><ispartof>The Journal of physiology, 2002-06, Vol.541 (3), p.917-928</ispartof><rights>2002 The Journal of Physiology © 2002 The Physiological Society</rights><rights>The Physiological Society 2002 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5517-ea2d12074c573743a7650856c5406ffd6781a952a3915b4b8dd4f0fedd35b5893</citedby><cites>FETCH-LOGICAL-c5517-ea2d12074c573743a7650856c5406ffd6781a952a3915b4b8dd4f0fedd35b5893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2290357/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2290357/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12068050$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hirst, G. D. S.</creatorcontrib><creatorcontrib>Dickens, E. J.</creatorcontrib><creatorcontrib>Edwards, F. R.</creatorcontrib><title>Pacemaker shift in the gastric antrum of guinea-pigs produced by excitatory vagal stimulation involves intramuscular interstitial cells</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>Intracellular recordings were made from isolated bundles of the circular muscle layer of guinea-pig gastric antrum and the
responses produced by stimulating intrinsic nerve fibres were examined. After abolishing the effects of stimulating inhibitory
nerve terminals with apamin and l -nitroarginine (NOLA), transmural nerve stimulation often evoked a small amplitude excitatory junction potential (EJP) and
invariably evoked a regenerative potential. Neurally evoked regenerative potentials had similar properties to those evoked
in the same bundle by direct stimulation. EJPs and neurally evoked regenerative potentials were abolished by hyoscine suggesting
that both resulted from the release of acetylcholine and activation of muscarinic receptors. Neurally evoked regenerative
potentials, but not EJPs, were abolished by membrane hyperpolarization, caffeine and chloride channel blockers. In the intact
antrum, excitatory vagal nerve stimulation increased the frequency of slow waves. Simultaneous intracellular recordings of
pacemaker potentials from myenteric interstitial cells (ICC MY ) and slow waves showed that the onset of each pacemaker potential normally preceded the onset of each slow wave but vagal
stimulation caused the onset of each slow wave to precede each pacemaker potential. Together the observations suggest that
during vagal stimulation there is a change in the origin of pacemaker activity with slow waves being initiated by intramuscular
interstitial cells (ICC IM ) rather than by ICC MY .</description><subject>4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid - pharmacology</subject><subject>Animals</subject><subject>Apamin - pharmacology</subject><subject>Biological Clocks - physiology</subject><subject>Boron Compounds - pharmacology</subject><subject>Electric Stimulation</subject><subject>Evoked Potentials - drug effects</subject><subject>Evoked Potentials - physiology</subject><subject>Excitatory Postsynaptic Potentials - drug effects</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>Female</subject><subject>Guinea Pigs</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Membrane Potentials - physiology</subject><subject>Muscarinic Antagonists - pharmacology</subject><subject>Muscle, Smooth - cytology</subject><subject>Muscle, Smooth - innervation</subject><subject>Muscle, Smooth - physiology</subject><subject>Nerve Endings - physiology</subject><subject>Nitroarginine - pharmacology</subject><subject>Original</subject><subject>Pyloric Antrum - innervation</subject><subject>Pyloric Antrum - physiology</subject><subject>Scopolamine - pharmacology</subject><subject>Stomach - cytology</subject><subject>Stomach - innervation</subject><subject>Stomach - physiology</subject><subject>Vagus Nerve - physiology</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u3SAQhVHVqLm97RtUFat25RswxtibSlWU_ilSskjXCOOxTWobF_BN_QR97WL59m-XFaD55swZDkKvKDlQStnF_dQt3tj-kBKSHggtcpo9QTua5WUiRMmeol0spAkTnJ6j597fE0IZKctn6JymJC8IJzv081ZpGNQ3cNh3pgnYjDh0gFvlgzMaqzG4ecC2we1sRlDJZFqPJ2frWUONqwXDD22CCtYt-Kha1WMfzDD3Khg7RrWj7Y_g4yU4Ncxex4pbX-AiF0zkNfS9f4HOGtV7eHk69-jrh6u7y0_J9c3Hz5fvrxPNORUJqLSO5kWmuWAiY0rknBQ81zwjedPUuSioKnmqWEl5lVVFXWcNaaCuGa94UbI9erfpTnM1QK1h9dXLyZlBuUVaZeT_ldF0srVHmaYlYXHoHr05CTj7fQYf5GD8uoIawc5eClqkPP5zBLMN1M5676D5M4QSuSYofyco1wTllmBse_2vwb9Np8giUGzAg-lheZSovPtyW9LV-9uttTNt92AcyA32VhsIi-QZlUyu5C-u7L5T</recordid><startdate>20020615</startdate><enddate>20020615</enddate><creator>Hirst, G. D. S.</creator><creator>Dickens, E. J.</creator><creator>Edwards, F. R.</creator><general>The Physiological Society</general><general>Blackwell Publishing Ltd</general><general>Blackwell Science Inc</general><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><scope>5PM</scope></search><sort><creationdate>20020615</creationdate><title>Pacemaker shift in the gastric antrum of guinea-pigs produced by excitatory vagal stimulation involves intramuscular interstitial cells</title><author>Hirst, G. D. S. ; Dickens, E. J. ; Edwards, F. R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5517-ea2d12074c573743a7650856c5406ffd6781a952a3915b4b8dd4f0fedd35b5893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid - pharmacology</topic><topic>Animals</topic><topic>Apamin - pharmacology</topic><topic>Biological Clocks - physiology</topic><topic>Boron Compounds - pharmacology</topic><topic>Electric Stimulation</topic><topic>Evoked Potentials - drug effects</topic><topic>Evoked Potentials - physiology</topic><topic>Excitatory Postsynaptic Potentials - drug effects</topic><topic>Excitatory Postsynaptic Potentials - physiology</topic><topic>Female</topic><topic>Guinea Pigs</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Membrane Potentials - physiology</topic><topic>Muscarinic Antagonists - pharmacology</topic><topic>Muscle, Smooth - cytology</topic><topic>Muscle, Smooth - innervation</topic><topic>Muscle, Smooth - physiology</topic><topic>Nerve Endings - physiology</topic><topic>Nitroarginine - pharmacology</topic><topic>Original</topic><topic>Pyloric Antrum - innervation</topic><topic>Pyloric Antrum - physiology</topic><topic>Scopolamine - pharmacology</topic><topic>Stomach - cytology</topic><topic>Stomach - innervation</topic><topic>Stomach - physiology</topic><topic>Vagus Nerve - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hirst, G. D. S.</creatorcontrib><creatorcontrib>Dickens, E. J.</creatorcontrib><creatorcontrib>Edwards, F. R.</creatorcontrib><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><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>Hirst, G. D. S.</au><au>Dickens, E. J.</au><au>Edwards, F. R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pacemaker shift in the gastric antrum of guinea-pigs produced by excitatory vagal stimulation involves intramuscular interstitial cells</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>2002-06-15</date><risdate>2002</risdate><volume>541</volume><issue>3</issue><spage>917</spage><epage>928</epage><pages>917-928</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>Intracellular recordings were made from isolated bundles of the circular muscle layer of guinea-pig gastric antrum and the
responses produced by stimulating intrinsic nerve fibres were examined. After abolishing the effects of stimulating inhibitory
nerve terminals with apamin and l -nitroarginine (NOLA), transmural nerve stimulation often evoked a small amplitude excitatory junction potential (EJP) and
invariably evoked a regenerative potential. Neurally evoked regenerative potentials had similar properties to those evoked
in the same bundle by direct stimulation. EJPs and neurally evoked regenerative potentials were abolished by hyoscine suggesting
that both resulted from the release of acetylcholine and activation of muscarinic receptors. Neurally evoked regenerative
potentials, but not EJPs, were abolished by membrane hyperpolarization, caffeine and chloride channel blockers. In the intact
antrum, excitatory vagal nerve stimulation increased the frequency of slow waves. Simultaneous intracellular recordings of
pacemaker potentials from myenteric interstitial cells (ICC MY ) and slow waves showed that the onset of each pacemaker potential normally preceded the onset of each slow wave but vagal
stimulation caused the onset of each slow wave to precede each pacemaker potential. Together the observations suggest that
during vagal stimulation there is a change in the origin of pacemaker activity with slow waves being initiated by intramuscular
interstitial cells (ICC IM ) rather than by ICC MY .</abstract><cop>Oxford, UK</cop><pub>The Physiological Society</pub><pmid>12068050</pmid><doi>10.1113/jphysiol.2002.018614</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Access via Wiley Online Library; Wiley Free Content; IngentaConnect Free/Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid - pharmacology Animals Apamin - pharmacology Biological Clocks - physiology Boron Compounds - pharmacology Electric Stimulation Evoked Potentials - drug effects Evoked Potentials - physiology Excitatory Postsynaptic Potentials - drug effects Excitatory Postsynaptic Potentials - physiology Female Guinea Pigs In Vitro Techniques Male Membrane Potentials - physiology Muscarinic Antagonists - pharmacology Muscle, Smooth - cytology Muscle, Smooth - innervation Muscle, Smooth - physiology Nerve Endings - physiology Nitroarginine - pharmacology Original Pyloric Antrum - innervation Pyloric Antrum - physiology Scopolamine - pharmacology Stomach - cytology Stomach - innervation Stomach - physiology Vagus Nerve - physiology |
title | Pacemaker shift in the gastric antrum of guinea-pigs produced by excitatory vagal stimulation involves intramuscular interstitial cells |
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