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Multiple modes of GABAergic inhibition of rat cerebellar granule cells
Cerebellar granule cells are inhibited phasically by GABA released synaptically from Golgi cells, but are inhibited more powerfully by tonic activity of high affinity α 6 subunit-containing GABA A receptors. During development the tonic activity is generated by the accumulation of GABA released by...
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Published in: | The Journal of physiology 2003-04, Vol.548 (1), p.97-110 |
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creator | Rossi, David J Hamann, Martine Attwell, David |
description | Cerebellar granule cells are inhibited phasically by GABA released synaptically from Golgi cells, but are inhibited more powerfully
by tonic activity of high affinity α 6 subunit-containing GABA A receptors. During development the tonic activity is generated by the accumulation of GABA released by action potentials,
but in the adult the tonic activity is independent of action potentials. Here we show that in adult rats the tonic activation
of GABA A receptors is produced by non-vesicular transmitter release and is reduced by the activity of GAT-1 and GAT-3 GABA transporters,
demonstrating that alterations of GABA uptake will modulate information flow through granule cells. Acetylcholine (ACh) evokes
a large Ca 2+ -dependent but action potential-independent release of GABA, which activates α 6 subunit-containing GABA A receptors. These data show that three separate modes of transmitter release can activate GABA A receptors in adult cerebellar granule cells: action potential-evoked exocytotic GABA release, non-vesicular release, and
ACh-evoked Ca 2+ -dependent release independent of action potentials. The relative magnitudes of the inhibitory charge transfers generated
by action potential-evoked release (during high frequency stimulation of the mossy fibres), tonic inhibition and superfused
ACh are 1:3:12, indicating that tonic and ACh-mediated inhibition may play a major role in regulating granule cell firing. |
doi_str_mv | 10.1113/jphysiol.2002.036459 |
format | article |
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by tonic activity of high affinity α 6 subunit-containing GABA A receptors. During development the tonic activity is generated by the accumulation of GABA released by action potentials,
but in the adult the tonic activity is independent of action potentials. Here we show that in adult rats the tonic activation
of GABA A receptors is produced by non-vesicular transmitter release and is reduced by the activity of GAT-1 and GAT-3 GABA transporters,
demonstrating that alterations of GABA uptake will modulate information flow through granule cells. Acetylcholine (ACh) evokes
a large Ca 2+ -dependent but action potential-independent release of GABA, which activates α 6 subunit-containing GABA A receptors. These data show that three separate modes of transmitter release can activate GABA A receptors in adult cerebellar granule cells: action potential-evoked exocytotic GABA release, non-vesicular release, and
ACh-evoked Ca 2+ -dependent release independent of action potentials. The relative magnitudes of the inhibitory charge transfers generated
by action potential-evoked release (during high frequency stimulation of the mossy fibres), tonic inhibition and superfused
ACh are 1:3:12, indicating that tonic and ACh-mediated inhibition may play a major role in regulating granule cell firing.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/jphysiol.2002.036459</identifier><identifier>PMID: 12588900</identifier><language>eng</language><publisher>England: The Physiological Society</publisher><subject>Acetylcholine - pharmacology ; Action Potentials - drug effects ; Action Potentials - physiology ; Animals ; Bicuculline - pharmacology ; Cell Size - drug effects ; Cerebellum - cytology ; Cerebellum - metabolism ; Cerebellum - physiology ; Electric Stimulation ; Electrophysiology ; Enzyme Inhibitors - pharmacology ; Exocytosis - drug effects ; GABA Antagonists - pharmacology ; gamma-Aminobutyric Acid - metabolism ; gamma-Aminobutyric Acid - physiology ; In Vitro Techniques ; Membrane Potentials - physiology ; Neuroglia - drug effects ; Neuroglia - metabolism ; Neurons - metabolism ; Neurons - physiology ; Neurotransmitter Agents - metabolism ; Original ; Patch-Clamp Techniques ; Proton-Translocating ATPases - antagonists & inhibitors ; Proton-Translocating ATPases - metabolism ; Rats ; Rats, Sprague-Dawley ; Synaptic Transmission - physiology</subject><ispartof>The Journal of physiology, 2003-04, Vol.548 (1), p.97-110</ispartof><rights>The Physiological Society 2003 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-887ff292c4a5829768ca7ae0adb93bfca516064599a5f6a4710ddd504c860df83</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/PMC2342786/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2342786/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12588900$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rossi, David J</creatorcontrib><creatorcontrib>Hamann, Martine</creatorcontrib><creatorcontrib>Attwell, David</creatorcontrib><title>Multiple modes of GABAergic inhibition of rat cerebellar granule cells</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>Cerebellar granule cells are inhibited phasically by GABA released synaptically from Golgi cells, but are inhibited more powerfully
by tonic activity of high affinity α 6 subunit-containing GABA A receptors. During development the tonic activity is generated by the accumulation of GABA released by action potentials,
but in the adult the tonic activity is independent of action potentials. Here we show that in adult rats the tonic activation
of GABA A receptors is produced by non-vesicular transmitter release and is reduced by the activity of GAT-1 and GAT-3 GABA transporters,
demonstrating that alterations of GABA uptake will modulate information flow through granule cells. Acetylcholine (ACh) evokes
a large Ca 2+ -dependent but action potential-independent release of GABA, which activates α 6 subunit-containing GABA A receptors. These data show that three separate modes of transmitter release can activate GABA A receptors in adult cerebellar granule cells: action potential-evoked exocytotic GABA release, non-vesicular release, and
ACh-evoked Ca 2+ -dependent release independent of action potentials. The relative magnitudes of the inhibitory charge transfers generated
by action potential-evoked release (during high frequency stimulation of the mossy fibres), tonic inhibition and superfused
ACh are 1:3:12, indicating that tonic and ACh-mediated inhibition may play a major role in regulating granule cell firing.</description><subject>Acetylcholine - pharmacology</subject><subject>Action Potentials - drug effects</subject><subject>Action Potentials - physiology</subject><subject>Animals</subject><subject>Bicuculline - pharmacology</subject><subject>Cell Size - drug effects</subject><subject>Cerebellum - cytology</subject><subject>Cerebellum - metabolism</subject><subject>Cerebellum - physiology</subject><subject>Electric Stimulation</subject><subject>Electrophysiology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Exocytosis - drug effects</subject><subject>GABA Antagonists - pharmacology</subject><subject>gamma-Aminobutyric Acid - metabolism</subject><subject>gamma-Aminobutyric Acid - physiology</subject><subject>In Vitro Techniques</subject><subject>Membrane Potentials - physiology</subject><subject>Neuroglia - drug effects</subject><subject>Neuroglia - metabolism</subject><subject>Neurons - metabolism</subject><subject>Neurons - physiology</subject><subject>Neurotransmitter Agents - metabolism</subject><subject>Original</subject><subject>Patch-Clamp Techniques</subject><subject>Proton-Translocating ATPases - antagonists & inhibitors</subject><subject>Proton-Translocating ATPases - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Synaptic Transmission - physiology</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpVUclOwzAQtRAIyvIHCOXELcX7ckEqFZsE4gJny3GcxiiNi52A-vcktGyn0cyb92Z5AJwiOEUIkYvXVb1OPjRTDCGeQsIpUztggihXuRCK7ILJAOCcCIYOwGFKrxAiApXaBwcIMykVhBNw89g3nV81LluG0qUsVNnt7Grm4sLbzLe1L3znQzvWo-ky66IrXNOYmC2iafuBZ4c0HYO9yjTJnWzjEXi5uX6e3-UPT7f389lDbhnmXS6lqCqssKWGSawEl9YI46ApC0WKyhqGOBwPUYZV3FCBYFmWDFIrOSwrSY7A5UZ31RdLV1rXdtE0ehX90sS1Dsbr_0jra70I7xoTioXkg8D5ViCGt96lTi99Gk8wrQt90oIgTtFXI9002hhSiq76GYKgHg3Q3wbo0QC9MWCgnf1d8Je0_fjvArVf1B8-Or2RScF61601o1IjrQT5BHSZkuE</recordid><startdate>20030401</startdate><enddate>20030401</enddate><creator>Rossi, David J</creator><creator>Hamann, Martine</creator><creator>Attwell, David</creator><general>The Physiological Society</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>20030401</creationdate><title>Multiple modes of GABAergic inhibition of rat cerebellar granule cells</title><author>Rossi, David J ; Hamann, Martine ; Attwell, David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-887ff292c4a5829768ca7ae0adb93bfca516064599a5f6a4710ddd504c860df83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Acetylcholine - pharmacology</topic><topic>Action Potentials - drug effects</topic><topic>Action Potentials - physiology</topic><topic>Animals</topic><topic>Bicuculline - pharmacology</topic><topic>Cell Size - drug effects</topic><topic>Cerebellum - cytology</topic><topic>Cerebellum - metabolism</topic><topic>Cerebellum - physiology</topic><topic>Electric Stimulation</topic><topic>Electrophysiology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Exocytosis - drug effects</topic><topic>GABA Antagonists - pharmacology</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>gamma-Aminobutyric Acid - physiology</topic><topic>In Vitro Techniques</topic><topic>Membrane Potentials - physiology</topic><topic>Neuroglia - drug effects</topic><topic>Neuroglia - metabolism</topic><topic>Neurons - metabolism</topic><topic>Neurons - physiology</topic><topic>Neurotransmitter Agents - metabolism</topic><topic>Original</topic><topic>Patch-Clamp Techniques</topic><topic>Proton-Translocating ATPases - antagonists & inhibitors</topic><topic>Proton-Translocating ATPases - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Synaptic Transmission - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rossi, David J</creatorcontrib><creatorcontrib>Hamann, Martine</creatorcontrib><creatorcontrib>Attwell, David</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>Rossi, David J</au><au>Hamann, Martine</au><au>Attwell, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multiple modes of GABAergic inhibition of rat cerebellar granule cells</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>2003-04-01</date><risdate>2003</risdate><volume>548</volume><issue>1</issue><spage>97</spage><epage>110</epage><pages>97-110</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>Cerebellar granule cells are inhibited phasically by GABA released synaptically from Golgi cells, but are inhibited more powerfully
by tonic activity of high affinity α 6 subunit-containing GABA A receptors. During development the tonic activity is generated by the accumulation of GABA released by action potentials,
but in the adult the tonic activity is independent of action potentials. Here we show that in adult rats the tonic activation
of GABA A receptors is produced by non-vesicular transmitter release and is reduced by the activity of GAT-1 and GAT-3 GABA transporters,
demonstrating that alterations of GABA uptake will modulate information flow through granule cells. Acetylcholine (ACh) evokes
a large Ca 2+ -dependent but action potential-independent release of GABA, which activates α 6 subunit-containing GABA A receptors. These data show that three separate modes of transmitter release can activate GABA A receptors in adult cerebellar granule cells: action potential-evoked exocytotic GABA release, non-vesicular release, and
ACh-evoked Ca 2+ -dependent release independent of action potentials. The relative magnitudes of the inhibitory charge transfers generated
by action potential-evoked release (during high frequency stimulation of the mossy fibres), tonic inhibition and superfused
ACh are 1:3:12, indicating that tonic and ACh-mediated inhibition may play a major role in regulating granule cell firing.</abstract><cop>England</cop><pub>The Physiological Society</pub><pmid>12588900</pmid><doi>10.1113/jphysiol.2002.036459</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylcholine - pharmacology Action Potentials - drug effects Action Potentials - physiology Animals Bicuculline - pharmacology Cell Size - drug effects Cerebellum - cytology Cerebellum - metabolism Cerebellum - physiology Electric Stimulation Electrophysiology Enzyme Inhibitors - pharmacology Exocytosis - drug effects GABA Antagonists - pharmacology gamma-Aminobutyric Acid - metabolism gamma-Aminobutyric Acid - physiology In Vitro Techniques Membrane Potentials - physiology Neuroglia - drug effects Neuroglia - metabolism Neurons - metabolism Neurons - physiology Neurotransmitter Agents - metabolism Original Patch-Clamp Techniques Proton-Translocating ATPases - antagonists & inhibitors Proton-Translocating ATPases - metabolism Rats Rats, Sprague-Dawley Synaptic Transmission - physiology |
title | Multiple modes of GABAergic inhibition of rat cerebellar granule cells |
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