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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Veröffentlicht in:The Journal of physiology 2002-06, Vol.541 (3), p.917-928
Hauptverfasser: Hirst, G. D. S., Dickens, E. J., Edwards, F. R.
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Dickens, E. J.
Edwards, F. R.
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 .
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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. 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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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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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