Activation of postsynaptic D2 dopamine receptors in the rat dorsolateral striatum prevents the amnestic effect of systemically administered neuroleptics

•The dorsolateral striatum mediates amnestic effects of neuroleptics.•This effect of neuroleptics depends on postsynaptic D2 receptors.•Avoidance learning needs fine-tuned balance of direct and indirect pathways. Systemically administered antipsychotics bind to dopamine (DA) D2 receptors expressed i...

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Veröffentlicht in:Behavioural brain research 2015-03, Vol.281, p.283-289
Hauptverfasser: Boschen, Suelen Lucio, Andreatini, Roberto, da Cunha, Claudio
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Andreatini, Roberto
da Cunha, Claudio
description •The dorsolateral striatum mediates amnestic effects of neuroleptics.•This effect of neuroleptics depends on postsynaptic D2 receptors.•Avoidance learning needs fine-tuned balance of direct and indirect pathways. Systemically administered antipsychotics bind to dopamine (DA) D2 receptors expressed in both pre- and postsynaptic neurons of different striatal sites and present an amnestic effect on learning and memory of conditioned avoidance responses (CAR). The aim of this study was to test whether blockade of the pre- or post-synaptic D2 receptors of the dorsolateral striatum of rats is the mechanism by which systemically administered antipsychotics present this amnestic effect. CAR learning and memory was evaluated in rats that received i.p. administrations of pre- or postsynaptic doses of the antipsychotic sulpiride combined with intra-DLS infusion of the D2 agonist quinpirole. Intra-DLS quinpirole itself was not amnestic and this effect was prevented by co-administration of presynaptic dose of sulpiride. However, sulpiride was amnestic when administered systemically in a post- but not presynaptic dose. This amnestic effect of sulpiride was prevented by the co-administration of quinpirole into the DLS. These results show that a blockade of postsynaptic D2 receptors in the DLS is necessary and sufficient to produce the amnestic effect of neuroleptics on CARs.
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Systemically administered antipsychotics bind to dopamine (DA) D2 receptors expressed in both pre- and postsynaptic neurons of different striatal sites and present an amnestic effect on learning and memory of conditioned avoidance responses (CAR). The aim of this study was to test whether blockade of the pre- or post-synaptic D2 receptors of the dorsolateral striatum of rats is the mechanism by which systemically administered antipsychotics present this amnestic effect. CAR learning and memory was evaluated in rats that received i.p. administrations of pre- or postsynaptic doses of the antipsychotic sulpiride combined with intra-DLS infusion of the D2 agonist quinpirole. Intra-DLS quinpirole itself was not amnestic and this effect was prevented by co-administration of presynaptic dose of sulpiride. However, sulpiride was amnestic when administered systemically in a post- but not presynaptic dose. 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Systemically administered antipsychotics bind to dopamine (DA) D2 receptors expressed in both pre- and postsynaptic neurons of different striatal sites and present an amnestic effect on learning and memory of conditioned avoidance responses (CAR). The aim of this study was to test whether blockade of the pre- or post-synaptic D2 receptors of the dorsolateral striatum of rats is the mechanism by which systemically administered antipsychotics present this amnestic effect. CAR learning and memory was evaluated in rats that received i.p. administrations of pre- or postsynaptic doses of the antipsychotic sulpiride combined with intra-DLS infusion of the D2 agonist quinpirole. Intra-DLS quinpirole itself was not amnestic and this effect was prevented by co-administration of presynaptic dose of sulpiride. However, sulpiride was amnestic when administered systemically in a post- but not presynaptic dose. This amnestic effect of sulpiride was prevented by the co-administration of quinpirole into the DLS. These results show that a blockade of postsynaptic D2 receptors in the DLS is necessary and sufficient to produce the amnestic effect of neuroleptics on CARs.</description><subject>Action-selection</subject><subject>Animals</subject><subject>Antipsychotic Agents - administration &amp; dosage</subject><subject>Antipsychotic Agents - pharmacology</subject><subject>Avoidance Learning - drug effects</subject><subject>Basal ganglia</subject><subject>Conditioning, Operant - drug effects</subject><subject>Corpus Striatum - drug effects</subject><subject>Dopamine D2 Receptor Antagonists - pharmacology</subject><subject>Drug Therapy, Combination</subject><subject>Male</subject><subject>Memory - drug effects</subject><subject>Neuroleptic</subject><subject>Neurons - drug effects</subject><subject>Quinpirole - administration &amp; dosage</subject><subject>Quinpirole - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Dopamine D2 - agonists</subject><subject>Receptors, Dopamine D2 - metabolism</subject><subject>Schizophrenia</subject><subject>Sulpiride - administration &amp; dosage</subject><subject>Sulpiride - pharmacology</subject><subject>Synaptic Membranes - drug effects</subject><subject>Two-way active avoidance</subject><issn>0166-4328</issn><issn>1872-7549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1v1DAQhi1ERZeFH8AF-cglwR-xkxWnqnxKlXopZ8uxx8KrxA62s9L-E35uHbZwRFxmpPEz78z4RegNJS0lVL4_tuOYWkZo11LWko48Qzs69KzpRXd4jnaVkU3H2XCNXuZ8JKQigr5A10yITvas26FfN6b4ky4-BhwdXmIu-Rz0UrzBHxm2cdGzD4ATGFhKTBn7gMuPWtClvqYcJ10g6Qnnkrwu64yXBCcIJf_G9Bwgb2LgHJiyzcjnXGD2Rk_TGWtb5X0tJLA4wJriBNvw_ApdOT1leP2U9-j7508Pt1-bu_sv325v7hrDB1kaa4XUUhgAKrQgpl5YjwYxSAGUOzIyI_XQmYGT4WCp5Na58QCO2pGMvWZ8j95ddJcUf651VzX7bGCadIC4ZkVlz_lAD5z-BypYx-kW9oheUJNizgmcWpKfdTorStTmnTqq6p3avFOUqbp27Xn7JL-OM9i_HX_MqsCHCwD1P04eksrGQzBgfbWnKBv9P-QfAcbwrfc</recordid><startdate>20150315</startdate><enddate>20150315</enddate><creator>Boschen, Suelen Lucio</creator><creator>Andreatini, Roberto</creator><creator>da Cunha, Claudio</creator><general>Elsevier B.V</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>7QG</scope><scope>7TK</scope></search><sort><creationdate>20150315</creationdate><title>Activation of postsynaptic D2 dopamine receptors in the rat dorsolateral striatum prevents the amnestic effect of systemically administered neuroleptics</title><author>Boschen, Suelen Lucio ; 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dosage</topic><topic>Sulpiride - pharmacology</topic><topic>Synaptic Membranes - drug effects</topic><topic>Two-way active avoidance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boschen, Suelen Lucio</creatorcontrib><creatorcontrib>Andreatini, Roberto</creatorcontrib><creatorcontrib>da Cunha, Claudio</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>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Behavioural brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boschen, Suelen Lucio</au><au>Andreatini, Roberto</au><au>da Cunha, Claudio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activation of postsynaptic D2 dopamine receptors in the rat dorsolateral striatum prevents the amnestic effect of systemically administered neuroleptics</atitle><jtitle>Behavioural brain research</jtitle><addtitle>Behav Brain Res</addtitle><date>2015-03-15</date><risdate>2015</risdate><volume>281</volume><spage>283</spage><epage>289</epage><pages>283-289</pages><issn>0166-4328</issn><eissn>1872-7549</eissn><abstract>•The dorsolateral striatum mediates amnestic effects of neuroleptics.•This effect of neuroleptics depends on postsynaptic D2 receptors.•Avoidance learning needs fine-tuned balance of direct and indirect pathways. Systemically administered antipsychotics bind to dopamine (DA) D2 receptors expressed in both pre- and postsynaptic neurons of different striatal sites and present an amnestic effect on learning and memory of conditioned avoidance responses (CAR). The aim of this study was to test whether blockade of the pre- or post-synaptic D2 receptors of the dorsolateral striatum of rats is the mechanism by which systemically administered antipsychotics present this amnestic effect. CAR learning and memory was evaluated in rats that received i.p. administrations of pre- or postsynaptic doses of the antipsychotic sulpiride combined with intra-DLS infusion of the D2 agonist quinpirole. Intra-DLS quinpirole itself was not amnestic and this effect was prevented by co-administration of presynaptic dose of sulpiride. However, sulpiride was amnestic when administered systemically in a post- but not presynaptic dose. 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subjects Action-selection
Animals
Antipsychotic Agents - administration & dosage
Antipsychotic Agents - pharmacology
Avoidance Learning - drug effects
Basal ganglia
Conditioning, Operant - drug effects
Corpus Striatum - drug effects
Dopamine D2 Receptor Antagonists - pharmacology
Drug Therapy, Combination
Male
Memory - drug effects
Neuroleptic
Neurons - drug effects
Quinpirole - administration & dosage
Quinpirole - pharmacology
Rats
Rats, Wistar
Receptors, Dopamine D2 - agonists
Receptors, Dopamine D2 - metabolism
Schizophrenia
Sulpiride - administration & dosage
Sulpiride - pharmacology
Synaptic Membranes - drug effects
Two-way active avoidance
title Activation of postsynaptic D2 dopamine receptors in the rat dorsolateral striatum prevents the amnestic effect of systemically administered neuroleptics
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