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Trace amine-associated receptor 1 modulates motor hyperactivity, cognition, and anxiety-like behavior in an animal model of ADHD
Trace amine-associated receptor 1 (TAAR1) is a G protein-coupled receptor that has recently been implicated in several psychiatric conditions related to monoaminergic dysfunction, such as schizophrenia, substance use disorders, and mood disorders. Although attention-deficit/hyperactivity disorder (A...
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Published in: | Progress in neuro-psychopharmacology & biological psychiatry 2022-07, Vol.117, p.110555-110555, Article 110555 |
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creator | Raony, Ícaro Domith, Ivan Lourenco, Mychael V. Paes-de-Carvalho, Roberto Pandolfo, Pablo |
description | Trace amine-associated receptor 1 (TAAR1) is a G protein-coupled receptor that has recently been implicated in several psychiatric conditions related to monoaminergic dysfunction, such as schizophrenia, substance use disorders, and mood disorders. Although attention-deficit/hyperactivity disorder (ADHD) is also related to changes in monoaminergic neurotransmission, studies that assess whether TAAR1 participates in the neurobiology of ADHD are lacking. We hypothesized that TAAR1 plays an important role in ADHD and might represent a potential therapeutic target. Here, we investigate if TAAR1 modulates behavioral phenotypes in Spontaneously Hypertensive Rats (SHR), the most validated animal model of ADHD, and Wistar Kyoto rats (WKY, used as a control strain). Our results showed that TAAR1 is downregulated in ADHD-related brain regions in SHR compared with WKY. While intracerebroventricular (i.c.v.) administration of the selective TAAR1 antagonist EPPTB impaired cognitive performance in SHR, i.c.v. administration of highly selective TAAR1 full agonist RO5256390 decreased motor hyperactivity, novelty-induced locomotion, and induced an anxiolytic-like behavior. Overall, our findings show that changes in TAAR1 levels/activity underlie behavior in SHR, suggesting that TAAR1 plays a role in the neurobiology of ADHD. Although additional confirmatory studies are required, TAAR1 might be a potential pharmacological target for individuals with this disorder.
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•Spontaneously Hypertensive Rats (SHR) are the most validated animal model of ADHD.•TAAR1 levels are downregulated in ADHD-related brain regions of SHR.•TAAR1 inhibition impairs cognitive performance in SHR.•TAAR1 activation decreases motor hyperactivity and anxiety-like behaviors in SHR.•TAAR1 is a potential pharmacological target for managing ADHD. |
doi_str_mv | 10.1016/j.pnpbp.2022.110555 |
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[Display omitted]
•Spontaneously Hypertensive Rats (SHR) are the most validated animal model of ADHD.•TAAR1 levels are downregulated in ADHD-related brain regions of SHR.•TAAR1 inhibition impairs cognitive performance in SHR.•TAAR1 activation decreases motor hyperactivity and anxiety-like behaviors in SHR.•TAAR1 is a potential pharmacological target for managing ADHD.</description><identifier>ISSN: 0278-5846</identifier><identifier>EISSN: 1878-4216</identifier><identifier>DOI: 10.1016/j.pnpbp.2022.110555</identifier><identifier>PMID: 35346791</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Animals ; Anxiety ; Anxiety - drug therapy ; Attention Deficit Disorder with Hyperactivity - psychology ; Attention-deficit/hyperactivity disorder ; Behavior ; Behavior, Animal ; Cognition ; Disease Models, Animal ; Hyperkinesis ; Psychomotor Agitation ; Rats ; Rats, Inbred SHR ; Rats, Inbred WKY ; Receptors, G-Protein-Coupled ; Trace amine associated receptor 1</subject><ispartof>Progress in neuro-psychopharmacology & biological psychiatry, 2022-07, Vol.117, p.110555-110555, Article 110555</ispartof><rights>2022 Elsevier Inc.</rights><rights>Copyright © 2022 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c289t-8b27d7f618e726b55fe713d936bac98cf48d67c2633b69126639763e5fa8332f3</citedby><cites>FETCH-LOGICAL-c289t-8b27d7f618e726b55fe713d936bac98cf48d67c2633b69126639763e5fa8332f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35346791$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raony, Ícaro</creatorcontrib><creatorcontrib>Domith, Ivan</creatorcontrib><creatorcontrib>Lourenco, Mychael V.</creatorcontrib><creatorcontrib>Paes-de-Carvalho, Roberto</creatorcontrib><creatorcontrib>Pandolfo, Pablo</creatorcontrib><title>Trace amine-associated receptor 1 modulates motor hyperactivity, cognition, and anxiety-like behavior in an animal model of ADHD</title><title>Progress in neuro-psychopharmacology & biological psychiatry</title><addtitle>Prog Neuropsychopharmacol Biol Psychiatry</addtitle><description>Trace amine-associated receptor 1 (TAAR1) is a G protein-coupled receptor that has recently been implicated in several psychiatric conditions related to monoaminergic dysfunction, such as schizophrenia, substance use disorders, and mood disorders. Although attention-deficit/hyperactivity disorder (ADHD) is also related to changes in monoaminergic neurotransmission, studies that assess whether TAAR1 participates in the neurobiology of ADHD are lacking. We hypothesized that TAAR1 plays an important role in ADHD and might represent a potential therapeutic target. Here, we investigate if TAAR1 modulates behavioral phenotypes in Spontaneously Hypertensive Rats (SHR), the most validated animal model of ADHD, and Wistar Kyoto rats (WKY, used as a control strain). Our results showed that TAAR1 is downregulated in ADHD-related brain regions in SHR compared with WKY. While intracerebroventricular (i.c.v.) administration of the selective TAAR1 antagonist EPPTB impaired cognitive performance in SHR, i.c.v. administration of highly selective TAAR1 full agonist RO5256390 decreased motor hyperactivity, novelty-induced locomotion, and induced an anxiolytic-like behavior. Overall, our findings show that changes in TAAR1 levels/activity underlie behavior in SHR, suggesting that TAAR1 plays a role in the neurobiology of ADHD. Although additional confirmatory studies are required, TAAR1 might be a potential pharmacological target for individuals with this disorder.
[Display omitted]
•Spontaneously Hypertensive Rats (SHR) are the most validated animal model of ADHD.•TAAR1 levels are downregulated in ADHD-related brain regions of SHR.•TAAR1 inhibition impairs cognitive performance in SHR.•TAAR1 activation decreases motor hyperactivity and anxiety-like behaviors in SHR.•TAAR1 is a potential pharmacological target for managing ADHD.</description><subject>Animals</subject><subject>Anxiety</subject><subject>Anxiety - drug therapy</subject><subject>Attention Deficit Disorder with Hyperactivity - psychology</subject><subject>Attention-deficit/hyperactivity disorder</subject><subject>Behavior</subject><subject>Behavior, Animal</subject><subject>Cognition</subject><subject>Disease Models, Animal</subject><subject>Hyperkinesis</subject><subject>Psychomotor Agitation</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Rats, Inbred WKY</subject><subject>Receptors, G-Protein-Coupled</subject><subject>Trace amine associated receptor 1</subject><issn>0278-5846</issn><issn>1878-4216</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kE1v1DAQhi0EotvCL0BCPnJotv6Oc-BQtbRFqsSlnC3HnlAvSRxs74q99afjZVuOSLY8mnnfGc-D0AdK1pRQdbFZL_PSL2tGGFtTSqSUr9CK6lY3glH1Gq0Iq7HUQp2g05w3hBDKCX-LTrjkQrUdXaGnh2QdYDuFGRqbc3TBFvA4gYOlxIQpnqLfjjWZa3TIPO4XqKYSdqHsz7GLP-ZQQpzPsZ19vb8DlH0zhp-Ae3i0u1A9Ya6FesJkx0NDGHEc8OX13fU79GawY4b3z-8Z-n7z5eHqrrn_dvv16vK-cUx3pdE9a307KKqhZaqXcoCWct9x1VvXaTcI7VXrmOK8Vx1lSvGuVRzkYDXnbOBn6NOx75Liry3kYqaQHYyjnSFus2FKiE5IIVSV8qPUpZhzgsEsqX487Q0l5oDebMxf9OaA3hzRV9fH5wHbfgL_z_PCugo-HwVQ19wFSCa7ALMDHyrtYnwM_x3wB1RjlnA</recordid><startdate>20220713</startdate><enddate>20220713</enddate><creator>Raony, Ícaro</creator><creator>Domith, Ivan</creator><creator>Lourenco, Mychael V.</creator><creator>Paes-de-Carvalho, Roberto</creator><creator>Pandolfo, Pablo</creator><general>Elsevier 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></search><sort><creationdate>20220713</creationdate><title>Trace amine-associated receptor 1 modulates motor hyperactivity, cognition, and anxiety-like behavior in an animal model of ADHD</title><author>Raony, Ícaro ; Domith, Ivan ; Lourenco, Mychael V. ; Paes-de-Carvalho, Roberto ; Pandolfo, Pablo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c289t-8b27d7f618e726b55fe713d936bac98cf48d67c2633b69126639763e5fa8332f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Anxiety</topic><topic>Anxiety - drug therapy</topic><topic>Attention Deficit Disorder with Hyperactivity - psychology</topic><topic>Attention-deficit/hyperactivity disorder</topic><topic>Behavior</topic><topic>Behavior, Animal</topic><topic>Cognition</topic><topic>Disease Models, Animal</topic><topic>Hyperkinesis</topic><topic>Psychomotor Agitation</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Rats, Inbred WKY</topic><topic>Receptors, G-Protein-Coupled</topic><topic>Trace amine associated receptor 1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raony, Ícaro</creatorcontrib><creatorcontrib>Domith, Ivan</creatorcontrib><creatorcontrib>Lourenco, Mychael V.</creatorcontrib><creatorcontrib>Paes-de-Carvalho, Roberto</creatorcontrib><creatorcontrib>Pandolfo, Pablo</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><jtitle>Progress in neuro-psychopharmacology & biological psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raony, Ícaro</au><au>Domith, Ivan</au><au>Lourenco, Mychael V.</au><au>Paes-de-Carvalho, Roberto</au><au>Pandolfo, Pablo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trace amine-associated receptor 1 modulates motor hyperactivity, cognition, and anxiety-like behavior in an animal model of ADHD</atitle><jtitle>Progress in neuro-psychopharmacology & biological psychiatry</jtitle><addtitle>Prog Neuropsychopharmacol Biol Psychiatry</addtitle><date>2022-07-13</date><risdate>2022</risdate><volume>117</volume><spage>110555</spage><epage>110555</epage><pages>110555-110555</pages><artnum>110555</artnum><issn>0278-5846</issn><eissn>1878-4216</eissn><abstract>Trace amine-associated receptor 1 (TAAR1) is a G protein-coupled receptor that has recently been implicated in several psychiatric conditions related to monoaminergic dysfunction, such as schizophrenia, substance use disorders, and mood disorders. Although attention-deficit/hyperactivity disorder (ADHD) is also related to changes in monoaminergic neurotransmission, studies that assess whether TAAR1 participates in the neurobiology of ADHD are lacking. We hypothesized that TAAR1 plays an important role in ADHD and might represent a potential therapeutic target. Here, we investigate if TAAR1 modulates behavioral phenotypes in Spontaneously Hypertensive Rats (SHR), the most validated animal model of ADHD, and Wistar Kyoto rats (WKY, used as a control strain). Our results showed that TAAR1 is downregulated in ADHD-related brain regions in SHR compared with WKY. While intracerebroventricular (i.c.v.) administration of the selective TAAR1 antagonist EPPTB impaired cognitive performance in SHR, i.c.v. administration of highly selective TAAR1 full agonist RO5256390 decreased motor hyperactivity, novelty-induced locomotion, and induced an anxiolytic-like behavior. Overall, our findings show that changes in TAAR1 levels/activity underlie behavior in SHR, suggesting that TAAR1 plays a role in the neurobiology of ADHD. Although additional confirmatory studies are required, TAAR1 might be a potential pharmacological target for individuals with this disorder.
[Display omitted]
•Spontaneously Hypertensive Rats (SHR) are the most validated animal model of ADHD.•TAAR1 levels are downregulated in ADHD-related brain regions of SHR.•TAAR1 inhibition impairs cognitive performance in SHR.•TAAR1 activation decreases motor hyperactivity and anxiety-like behaviors in SHR.•TAAR1 is a potential pharmacological target for managing ADHD.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>35346791</pmid><doi>10.1016/j.pnpbp.2022.110555</doi><tpages>1</tpages></addata></record> |
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subjects | Animals Anxiety Anxiety - drug therapy Attention Deficit Disorder with Hyperactivity - psychology Attention-deficit/hyperactivity disorder Behavior Behavior, Animal Cognition Disease Models, Animal Hyperkinesis Psychomotor Agitation Rats Rats, Inbred SHR Rats, Inbred WKY Receptors, G-Protein-Coupled Trace amine associated receptor 1 |
title | Trace amine-associated receptor 1 modulates motor hyperactivity, cognition, and anxiety-like behavior in an animal model of ADHD |
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