Context and topography determine the role of basolateral amygdala metabotropic glutamate receptor 5 in appetitive Pavlovian responding
Preclinical data have shown that the excitatory metabotropic Gα -coupled glutamate receptor, mGluR5, has a role in substance abuse and relapse. However, little is known about the contribution of mGluR5 to the expression of conditioned responding elicited by appetitive Pavlovian cues. We investigated...
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description | Preclinical data have shown that the excitatory metabotropic Gα
-coupled glutamate receptor, mGluR5, has a role in substance abuse and relapse. However, little is known about the contribution of mGluR5 to the expression of conditioned responding elicited by appetitive Pavlovian cues. We investigated this question in rats that were trained to associate a discrete, auditory conditioned stimulus (CS) with a fructose-glucose solution (5.5% fructose/4.5% glucose; "sugar"). In subsequent tests for the expression of conditioned responding without sugar delivery, CS-elicited fluid port entries were elevated in a context associated with sugar, relative to an equally familiar, neutral context. Inhibiting mGluR5 via systemic injections of a negative allosteric modulator (MTEP; 5 mg/kg) reduced CS port entries in both the sugar context and neutral context. Targeting MTEP microinjections (3 µg/side; 0.3 µl/min) to the nucleus accumbens (Acb) core had no effect on CS port entries at test, whereas the same manipulation in the basolateral amygdala (BLA) produced effects that were topographically dependent. Specifically, microinjecting MTEP in the posterior BLA had no effect on behavior, whereas inhibiting mGluR5 in the anterior BLA enhanced the contextual discrimination of CS port entries. These data are the first to show a role of mGluR5 in the context-dependent expression of appetitive Pavlovian conditioned responding, with a topographically defined arrangement of mGluR5 in the BLA being particularly important for context-based responding to a discrete, appetitive cue. |
doi_str_mv | 10.1038/s41386-019-0335-6 |
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-coupled glutamate receptor, mGluR5, has a role in substance abuse and relapse. However, little is known about the contribution of mGluR5 to the expression of conditioned responding elicited by appetitive Pavlovian cues. We investigated this question in rats that were trained to associate a discrete, auditory conditioned stimulus (CS) with a fructose-glucose solution (5.5% fructose/4.5% glucose; "sugar"). In subsequent tests for the expression of conditioned responding without sugar delivery, CS-elicited fluid port entries were elevated in a context associated with sugar, relative to an equally familiar, neutral context. Inhibiting mGluR5 via systemic injections of a negative allosteric modulator (MTEP; 5 mg/kg) reduced CS port entries in both the sugar context and neutral context. Targeting MTEP microinjections (3 µg/side; 0.3 µl/min) to the nucleus accumbens (Acb) core had no effect on CS port entries at test, whereas the same manipulation in the basolateral amygdala (BLA) produced effects that were topographically dependent. Specifically, microinjecting MTEP in the posterior BLA had no effect on behavior, whereas inhibiting mGluR5 in the anterior BLA enhanced the contextual discrimination of CS port entries. These data are the first to show a role of mGluR5 in the context-dependent expression of appetitive Pavlovian conditioned responding, with a topographically defined arrangement of mGluR5 in the BLA being particularly important for context-based responding to a discrete, appetitive cue.</description><subject>Allosteric properties</subject><subject>Allosteric Regulation</subject><subject>Amygdala</subject><subject>Animal behavior</subject><subject>Animals</subject><subject>Appetitive Behavior - drug effects</subject><subject>Appetitive Behavior - physiology</subject><subject>Auditory discrimination</subject><subject>Basolateral Nuclear Complex - drug effects</subject><subject>Basolateral Nuclear Complex - metabolism</subject><subject>Brain</subject><subject>Conditioned stimulus</subject><subject>Conditioning</subject><subject>Conditioning, Classical - drug effects</subject><subject>Conditioning, Classical - physiology</subject><subject>Dizocilpine Maleate - pharmacology</subject><subject>Drug abuse</subject><subject>Excitatory Amino Acid Antagonists - pharmacology</subject><subject>Fructose</subject><subject>Glucose</subject><subject>Glutamic acid receptors (metabotropic)</subject><subject>Male</subject><subject>Nucleus accumbens</subject><subject>Pyridines - pharmacology</subject><subject>Rats, Long-Evans</subject><subject>Receptor, Metabotropic Glutamate 5 - antagonists & inhibitors</subject><subject>Receptor, Metabotropic Glutamate 5 - metabolism</subject><subject>Rodents</subject><subject>Sugar</subject><subject>Thiazoles - pharmacology</subject><issn>0893-133X</issn><issn>1740-634X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkc2O1DAQhCMEYoeFB-CCLHHhErDTceJckNCIP2klOIC0N6uTtDNeJXawnRHzAjw3Xs2yAk596K9KXV1F8Vzw14KDehNrAaopuehKDiDL5kGxE23Nywbq64fFjqsOSgFwfVE8ifGGcyHbRj0uLoC3UgGIXfFr712in4mhG1nyq58CrocTGylRWKwjlg7Egp-JecN6jH7GvMGZ4XKaRpyRLZSw9yn41Q5smreES0ZYoIHW5AOTzDqG60rJJnsk9hWPsz9adBmJq3ejddPT4pHBOdKzu3lZfP_w_tv-U3n15ePn_burcqirNpWqlXm2UBF1CARmEKoXCqU0okfViaFuuRTUN0bVSoGhRhmqhqzoAY2By-Lt2Xfd-oXGgVzKWfQa7ILhpD1a_e_G2YOe_FE3rZK8g2zw6s4g-B8bxaQXGweaZ3Tkt6groaTMXxYyoy__Q2_8FlyOp6tKKgE8Z8mUOFND8DEGMvfHCK5vW9bnlnVuWd-2rJusefF3invFn1rhNyAkpvY</recordid><startdate>20190801</startdate><enddate>20190801</enddate><creator>Khoo, Shaun Yon-Seng</creator><creator>LeCocq, Mandy Rita</creator><creator>Deyab, Ghislaine E</creator><creator>Chaudhri, Nadia</creator><general>Nature Publishing Group</general><general>Springer International Publishing</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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0972-3788</orcidid></search><sort><creationdate>20190801</creationdate><title>Context and topography determine the role of basolateral amygdala metabotropic glutamate receptor 5 in appetitive Pavlovian responding</title><author>Khoo, Shaun Yon-Seng ; 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subjects | Allosteric properties Allosteric Regulation Amygdala Animal behavior Animals Appetitive Behavior - drug effects Appetitive Behavior - physiology Auditory discrimination Basolateral Nuclear Complex - drug effects Basolateral Nuclear Complex - metabolism Brain Conditioned stimulus Conditioning Conditioning, Classical - drug effects Conditioning, Classical - physiology Dizocilpine Maleate - pharmacology Drug abuse Excitatory Amino Acid Antagonists - pharmacology Fructose Glucose Glutamic acid receptors (metabotropic) Male Nucleus accumbens Pyridines - pharmacology Rats, Long-Evans Receptor, Metabotropic Glutamate 5 - antagonists & inhibitors Receptor, Metabotropic Glutamate 5 - metabolism Rodents Sugar Thiazoles - pharmacology |
title | Context and topography determine the role of basolateral amygdala metabotropic glutamate receptor 5 in appetitive Pavlovian responding |
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