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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Veröffentlicht in:The European journal of neuroscience 2002-07, Vol.16 (2), p.350-354
Hauptverfasser: Poluch, Sylvie, König, Norbert
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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.
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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 &amp; 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 &amp; 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 &amp; 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 &amp; 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. 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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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