AMPA receptor activation induces GABA release from neurons migrating tangentially in the intermediate zone of embryonic rat neocortex
In the intermediate zone of the embryonic rodent neocortex, neurons migrating tangentially from the basal ganglia express both functional amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole propionic acid (AMPA) receptors and γ‐aminobutyric acid (GABA). To test the hypothesis of GABA release triggered by AMPA rece...
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description | In the intermediate zone of the embryonic rodent neocortex, neurons migrating tangentially from the basal ganglia express both functional amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole propionic acid (AMPA) receptors and γ‐aminobutyric acid (GABA). To test the hypothesis of GABA release triggered by AMPA receptor activation, we used whole‐hemisphere cultures prepared from rat embryos (day 15). We observed a marked decrease in the number of detectable GABA‐positive cells in the intermediate zone after exposure to T‐AMPA. This effect was blocked by coapplying GYKI 53655, an AMPA receptor antagonist. The decrease in GABA immunolabelling induced by T‐AMPA did not require extracellular calcium. In contrast, it was abolished after sodium substitution by choline, or after coapplication of nipecotic acid, a GABA transporter inhibitor. Exposure to high potassium reduced the number of detectable GABA‐positive cells. These results are compatible with carrier‐mediated GABA release consecutive to sodium influx. GABA released from neurons migrating tangentially in the intermediate zone after AMPA receptor activation may influence neighbouring elements including radially migrating postmitotic neurons, proliferating progenitors and possibly the tangential cells themselves. |
doi_str_mv | 10.1046/j.1460-9568.2002.02068.x |
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To test the hypothesis of GABA release triggered by AMPA receptor activation, we used whole‐hemisphere cultures prepared from rat embryos (day 15). We observed a marked decrease in the number of detectable GABA‐positive cells in the intermediate zone after exposure to T‐AMPA. This effect was blocked by coapplying GYKI 53655, an AMPA receptor antagonist. The decrease in GABA immunolabelling induced by T‐AMPA did not require extracellular calcium. In contrast, it was abolished after sodium substitution by choline, or after coapplication of nipecotic acid, a GABA transporter inhibitor. Exposure to high potassium reduced the number of detectable GABA‐positive cells. These results are compatible with carrier‐mediated GABA release consecutive to sodium influx. 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To test the hypothesis of GABA release triggered by AMPA receptor activation, we used whole‐hemisphere cultures prepared from rat embryos (day 15). We observed a marked decrease in the number of detectable GABA‐positive cells in the intermediate zone after exposure to T‐AMPA. This effect was blocked by coapplying GYKI 53655, an AMPA receptor antagonist. The decrease in GABA immunolabelling induced by T‐AMPA did not require extracellular calcium. In contrast, it was abolished after sodium substitution by choline, or after coapplication of nipecotic acid, a GABA transporter inhibitor. Exposure to high potassium reduced the number of detectable GABA‐positive cells. These results are compatible with carrier‐mediated GABA release consecutive to sodium influx. GABA released from neurons migrating tangentially in the intermediate zone after AMPA receptor activation may influence neighbouring elements including radially migrating postmitotic neurons, proliferating progenitors and possibly the tangential cells themselves.</description><subject>alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology</subject><subject>Animals</subject><subject>Calcium - deficiency</subject><subject>Carrier Proteins - antagonists & inhibitors</subject><subject>Carrier Proteins - metabolism</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Movement - drug effects</subject><subject>Cell Movement - physiology</subject><subject>development</subject><subject>Excitatory Amino Acid Antagonists - pharmacology</subject><subject>Female</subject><subject>Fetus</subject><subject>GABA Plasma Membrane Transport Proteins</subject><subject>GABA transporter</subject><subject>gamma-Aminobutyric Acid - metabolism</subject><subject>glutamate receptors</subject><subject>Immunohistochemistry</subject><subject>Membrane Proteins - antagonists & inhibitors</subject><subject>Membrane Proteins - metabolism</subject><subject>Membrane Transport Proteins</subject><subject>Microtubule-Associated Proteins - metabolism</subject><subject>Neocortex - cytology</subject><subject>Neocortex - embryology</subject><subject>Neocortex - metabolism</subject><subject>Neurons - cytology</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Nipecotic Acids - pharmacology</subject><subject>Organic Anion Transporters</subject><subject>Potassium - pharmacology</subject><subject>Pregnancy</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, AMPA - antagonists & inhibitors</subject><subject>Receptors, AMPA - metabolism</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - drug effects</subject><subject>Stem Cells - metabolism</subject><subject>Synaptic Transmission - drug effects</subject><subject>Synaptic Transmission - physiology</subject><subject>tangential migration</subject><subject>telencephalon</subject><issn>0953-816X</issn><issn>1460-9568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9vEzEQxS0EomnhKyCfEJcN_rPrtQ8cQlVSSimgguBmOc5scNhdB9vbJtz7vfGSqNwQF89Y_r0Z6z2EMCVTSkrxcj2lpSCFqoScMkLYlDCS2-0DNLl_eIgmRFW8kFR8O0LHMa4JIVKU1WN0RBkVilIxQXez9x9nOICFTfIBG5vcjUnO99j1y8FCxPPZ6xFowUTATfAd7mEIvo-4c6uQ2X6Fk-lX0Cdn2naXhTh9h1wShA6WziTAv3wP2DcYukXY-d5ZnJV5kLc-JNg-QY8a00Z4eqgn6Mubs8-n58Xlh_nb09llYSvCZKGsZIow4LWx0lphmaiqBcim4bQuRaOIgXyoJcCSclZlL_KNcaq4ocA4P0HP93M3wf8cICbduWihbU3-yhB1TZUsWUky-OKfIJXZSlGpss6o3KM2-BgDNHoTXGfCTlOix7T0Wo-h6DEUPaal_6Slt1n67LBlWGSn_goP8WTg1R64dS3s_nuwPru4GrusL_Z6F7PL93oTfmhR87rSX6_m-por-ulavtM1_w32qLOp</recordid><startdate>200207</startdate><enddate>200207</enddate><creator>Poluch, Sylvie</creator><creator>König, Norbert</creator><general>Blackwell Science, Ltd</general><scope>BSCLL</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></search><sort><creationdate>200207</creationdate><title>AMPA receptor activation induces GABA release from neurons migrating tangentially in the intermediate zone of embryonic rat neocortex</title><author>Poluch, Sylvie ; König, Norbert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5028-9c82902e37ac8cc6c2655be8ff31746f90aef909deed132514690923193a1e233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology</topic><topic>Animals</topic><topic>Calcium - deficiency</topic><topic>Carrier Proteins - antagonists & inhibitors</topic><topic>Carrier Proteins - metabolism</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Movement - drug effects</topic><topic>Cell Movement - physiology</topic><topic>development</topic><topic>Excitatory Amino Acid Antagonists - pharmacology</topic><topic>Female</topic><topic>Fetus</topic><topic>GABA Plasma Membrane Transport Proteins</topic><topic>GABA transporter</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>glutamate receptors</topic><topic>Immunohistochemistry</topic><topic>Membrane Proteins - antagonists & inhibitors</topic><topic>Membrane Proteins - metabolism</topic><topic>Membrane Transport Proteins</topic><topic>Microtubule-Associated Proteins - metabolism</topic><topic>Neocortex - cytology</topic><topic>Neocortex - embryology</topic><topic>Neocortex - metabolism</topic><topic>Neurons - cytology</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>Nipecotic Acids - pharmacology</topic><topic>Organic Anion Transporters</topic><topic>Potassium - pharmacology</topic><topic>Pregnancy</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, AMPA - antagonists & inhibitors</topic><topic>Receptors, AMPA - metabolism</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - drug effects</topic><topic>Stem Cells - metabolism</topic><topic>Synaptic Transmission - drug effects</topic><topic>Synaptic Transmission - physiology</topic><topic>tangential migration</topic><topic>telencephalon</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Poluch, Sylvie</creatorcontrib><creatorcontrib>König, Norbert</creatorcontrib><collection>Istex</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><jtitle>The European journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poluch, Sylvie</au><au>König, Norbert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AMPA receptor activation induces GABA release from neurons migrating tangentially in the intermediate zone of embryonic rat neocortex</atitle><jtitle>The European journal of neuroscience</jtitle><addtitle>Eur J Neurosci</addtitle><date>2002-07</date><risdate>2002</risdate><volume>16</volume><issue>2</issue><spage>350</spage><epage>354</epage><pages>350-354</pages><issn>0953-816X</issn><eissn>1460-9568</eissn><abstract>In the intermediate zone of the embryonic rodent neocortex, neurons migrating tangentially from the basal ganglia express both functional amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole propionic acid (AMPA) receptors and γ‐aminobutyric acid (GABA). To test the hypothesis of GABA release triggered by AMPA receptor activation, we used whole‐hemisphere cultures prepared from rat embryos (day 15). We observed a marked decrease in the number of detectable GABA‐positive cells in the intermediate zone after exposure to T‐AMPA. This effect was blocked by coapplying GYKI 53655, an AMPA receptor antagonist. The decrease in GABA immunolabelling induced by T‐AMPA did not require extracellular calcium. In contrast, it was abolished after sodium substitution by choline, or after coapplication of nipecotic acid, a GABA transporter inhibitor. Exposure to high potassium reduced the number of detectable GABA‐positive cells. These results are compatible with carrier‐mediated GABA release consecutive to sodium influx. GABA released from neurons migrating tangentially in the intermediate zone after AMPA receptor activation may influence neighbouring elements including radially migrating postmitotic neurons, proliferating progenitors and possibly the tangential cells themselves.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science, Ltd</pub><pmid>12169116</pmid><doi>10.1046/j.1460-9568.2002.02068.x</doi><tpages>5</tpages></addata></record> |
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subjects | alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - pharmacology Animals Calcium - deficiency Carrier Proteins - antagonists & inhibitors Carrier Proteins - metabolism Cell Differentiation - drug effects Cell Differentiation - physiology Cell Movement - drug effects Cell Movement - physiology development Excitatory Amino Acid Antagonists - pharmacology Female Fetus GABA Plasma Membrane Transport Proteins GABA transporter gamma-Aminobutyric Acid - metabolism glutamate receptors Immunohistochemistry Membrane Proteins - antagonists & inhibitors Membrane Proteins - metabolism Membrane Transport Proteins Microtubule-Associated Proteins - metabolism Neocortex - cytology Neocortex - embryology Neocortex - metabolism Neurons - cytology Neurons - drug effects Neurons - metabolism Nipecotic Acids - pharmacology Organic Anion Transporters Potassium - pharmacology Pregnancy Rats Rats, Sprague-Dawley Receptors, AMPA - antagonists & inhibitors Receptors, AMPA - metabolism Stem Cells - cytology Stem Cells - drug effects Stem Cells - metabolism Synaptic Transmission - drug effects Synaptic Transmission - physiology tangential migration telencephalon |
title | AMPA receptor activation induces GABA release from neurons migrating tangentially in the intermediate zone of embryonic rat neocortex |
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