INFLUENCE OF A2A TREATMENT ON DEPRESSIVE‑LIKE BEHAVIOR AND D2‑RECEPTOR AVAILABILITY IN RATS EXPOSED TO REPEATED SOCIAL DEFEAT
The interaction between the dopaminergic and adenosinergic systems in depressive phenotypes remains largely unexplored. This study aimed to investigate the effect of adenosine A2a receptor modulation on the development of depressive-like behavior and dopamine D2 receptor availability, in rats expose...
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Veröffentlicht in: | Acta neurobiologiae experimentalis 2022-01, Vol.82, p.LXXXVI |
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container_title | Acta neurobiologiae experimentalis |
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creator | Matias, Daniel A Vazquez Henry, Samia Guerrin, Cyprien GJ Prasad, Kavya Doorduin, Janine de Vries, Erik FJ |
description | The interaction between the dopaminergic and adenosinergic systems in depressive phenotypes remains largely unexplored. This study aimed to investigate the effect of adenosine A2a receptor modulation on the development of depressive-like behavior and dopamine D2 receptor availability, in rats exposed to repeated social defeat. Thirty-eight rats were divided into three groups which received vehicle, the A2A agonist CGS21680 (0.1 mg/kg), or the A2A antagonist KW6002 (1 mg/kg). Rats underwent 5 days of repeated social defeat using the resident intruder paradigm. Anhedonia-like and anxiety-like behavior were assessed using a sucrose preference and open field tests respectively to validate the depressive-like phenotype. D2 receptor availability in the striatal regions was assessed using [11C]raclopride-PET. Treatment with both CGS21680 and KW6002 prevented a decrease in sucrose preference and decreased locomotor activity after social defeat. Both drugs decreased D2 receptor availability in the striatum, in particular in caudate-putamen. A2AR-antagonist treatment also decreased it D2 receptor availability in the nucleus-accumbens. Our study showed that the treatment with either an A2AR agonist or an A2AR antagonist prevented the development of depressive-like behavior, and reduced the availability of D2R in the striatum after exposure to RSD. |
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This study aimed to investigate the effect of adenosine A2a receptor modulation on the development of depressive-like behavior and dopamine D2 receptor availability, in rats exposed to repeated social defeat. Thirty-eight rats were divided into three groups which received vehicle, the A2A agonist CGS21680 (0.1 mg/kg), or the A2A antagonist KW6002 (1 mg/kg). Rats underwent 5 days of repeated social defeat using the resident intruder paradigm. Anhedonia-like and anxiety-like behavior were assessed using a sucrose preference and open field tests respectively to validate the depressive-like phenotype. D2 receptor availability in the striatal regions was assessed using [11C]raclopride-PET. Treatment with both CGS21680 and KW6002 prevented a decrease in sucrose preference and decreased locomotor activity after social defeat. Both drugs decreased D2 receptor availability in the striatum, in particular in caudate-putamen. A2AR-antagonist treatment also decreased it D2 receptor availability in the nucleus-accumbens. Our study showed that the treatment with either an A2AR agonist or an A2AR antagonist prevented the development of depressive-like behavior, and reduced the availability of D2R in the striatum after exposure to RSD.</description><identifier>ISSN: 0065-1400</identifier><identifier>EISSN: 1689-0035</identifier><language>eng</language><publisher>Warsaw: Polish Academy of Sciences</publisher><subject>Adenosine ; Agonists ; Anxiety ; Availability ; Caudate-putamen ; Dopamine ; Dopamine D2 receptors ; Exposure ; Field tests ; Hedonic response ; Locomotor activity ; Neostriatum ; Nucleus accumbens ; Phenotypes ; Putamen ; Raclopride ; Receptors ; Social interactions ; Sucrose</subject><ispartof>Acta neurobiologiae experimentalis, 2022-01, Vol.82, p.LXXXVI</ispartof><rights>Copyright Polish Academy of Sciences 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids></links><search><creatorcontrib>Matias, Daniel A Vazquez</creatorcontrib><creatorcontrib>Henry, Samia</creatorcontrib><creatorcontrib>Guerrin, Cyprien GJ</creatorcontrib><creatorcontrib>Prasad, Kavya</creatorcontrib><creatorcontrib>Doorduin, Janine</creatorcontrib><creatorcontrib>de Vries, Erik FJ</creatorcontrib><title>INFLUENCE OF A2A TREATMENT ON DEPRESSIVE‑LIKE BEHAVIOR AND D2‑RECEPTOR AVAILABILITY IN RATS EXPOSED TO REPEATED SOCIAL DEFEAT</title><title>Acta neurobiologiae experimentalis</title><description>The interaction between the dopaminergic and adenosinergic systems in depressive phenotypes remains largely unexplored. This study aimed to investigate the effect of adenosine A2a receptor modulation on the development of depressive-like behavior and dopamine D2 receptor availability, in rats exposed to repeated social defeat. Thirty-eight rats were divided into three groups which received vehicle, the A2A agonist CGS21680 (0.1 mg/kg), or the A2A antagonist KW6002 (1 mg/kg). Rats underwent 5 days of repeated social defeat using the resident intruder paradigm. Anhedonia-like and anxiety-like behavior were assessed using a sucrose preference and open field tests respectively to validate the depressive-like phenotype. D2 receptor availability in the striatal regions was assessed using [11C]raclopride-PET. Treatment with both CGS21680 and KW6002 prevented a decrease in sucrose preference and decreased locomotor activity after social defeat. Both drugs decreased D2 receptor availability in the striatum, in particular in caudate-putamen. A2AR-antagonist treatment also decreased it D2 receptor availability in the nucleus-accumbens. Our study showed that the treatment with either an A2AR agonist or an A2AR antagonist prevented the development of depressive-like behavior, and reduced the availability of D2R in the striatum after exposure to RSD.</description><subject>Adenosine</subject><subject>Agonists</subject><subject>Anxiety</subject><subject>Availability</subject><subject>Caudate-putamen</subject><subject>Dopamine</subject><subject>Dopamine D2 receptors</subject><subject>Exposure</subject><subject>Field tests</subject><subject>Hedonic response</subject><subject>Locomotor activity</subject><subject>Neostriatum</subject><subject>Nucleus accumbens</subject><subject>Phenotypes</subject><subject>Putamen</subject><subject>Raclopride</subject><subject>Receptors</subject><subject>Social interactions</subject><subject>Sucrose</subject><issn>0065-1400</issn><issn>1689-0035</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqNjM1OwzAQhC0EEuHnHVbiHGnjkCY5bpONusLYkW0iOFUcyqFCFBp6h0fgFXkSjMQDcJqZb0ZzpLJi0bQ5YlkdqwxxUeXFNeKpOpvnLaKua42Z-hQ7mDu2HYMbgDRB9Ezxlm0EZ6Hn0XMIMvH3x5eRG4Ylr2gS54FsD71O2HPHY_wlE4mhpRiJDyAWPMUAfD-6wD1EB57HdJ18cJ2QSedDyhfq5Onxed5c_um5uho4dqv8db97O2zm9_V2d9i_pGqt66op2wLbpvzf6gclUkeK</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Matias, Daniel A Vazquez</creator><creator>Henry, Samia</creator><creator>Guerrin, Cyprien GJ</creator><creator>Prasad, Kavya</creator><creator>Doorduin, Janine</creator><creator>de Vries, Erik FJ</creator><general>Polish Academy of Sciences</general><scope>7QG</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20220101</creationdate><title>INFLUENCE OF A2A TREATMENT ON DEPRESSIVE‑LIKE BEHAVIOR AND D2‑RECEPTOR AVAILABILITY IN RATS EXPOSED TO REPEATED SOCIAL DEFEAT</title><author>Matias, Daniel A Vazquez ; Henry, Samia ; Guerrin, Cyprien GJ ; Prasad, Kavya ; Doorduin, Janine ; de Vries, Erik FJ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_27583910983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adenosine</topic><topic>Agonists</topic><topic>Anxiety</topic><topic>Availability</topic><topic>Caudate-putamen</topic><topic>Dopamine</topic><topic>Dopamine D2 receptors</topic><topic>Exposure</topic><topic>Field tests</topic><topic>Hedonic response</topic><topic>Locomotor activity</topic><topic>Neostriatum</topic><topic>Nucleus accumbens</topic><topic>Phenotypes</topic><topic>Putamen</topic><topic>Raclopride</topic><topic>Receptors</topic><topic>Social interactions</topic><topic>Sucrose</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matias, Daniel A Vazquez</creatorcontrib><creatorcontrib>Henry, Samia</creatorcontrib><creatorcontrib>Guerrin, Cyprien GJ</creatorcontrib><creatorcontrib>Prasad, Kavya</creatorcontrib><creatorcontrib>Doorduin, Janine</creatorcontrib><creatorcontrib>de Vries, Erik FJ</creatorcontrib><collection>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Acta neurobiologiae experimentalis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matias, Daniel A Vazquez</au><au>Henry, Samia</au><au>Guerrin, Cyprien GJ</au><au>Prasad, Kavya</au><au>Doorduin, Janine</au><au>de Vries, Erik FJ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>INFLUENCE OF A2A TREATMENT ON DEPRESSIVE‑LIKE BEHAVIOR AND D2‑RECEPTOR AVAILABILITY IN RATS EXPOSED TO REPEATED SOCIAL DEFEAT</atitle><jtitle>Acta neurobiologiae experimentalis</jtitle><date>2022-01-01</date><risdate>2022</risdate><volume>82</volume><spage>LXXXVI</spage><pages>LXXXVI-</pages><issn>0065-1400</issn><eissn>1689-0035</eissn><abstract>The interaction between the dopaminergic and adenosinergic systems in depressive phenotypes remains largely unexplored. This study aimed to investigate the effect of adenosine A2a receptor modulation on the development of depressive-like behavior and dopamine D2 receptor availability, in rats exposed to repeated social defeat. Thirty-eight rats were divided into three groups which received vehicle, the A2A agonist CGS21680 (0.1 mg/kg), or the A2A antagonist KW6002 (1 mg/kg). Rats underwent 5 days of repeated social defeat using the resident intruder paradigm. Anhedonia-like and anxiety-like behavior were assessed using a sucrose preference and open field tests respectively to validate the depressive-like phenotype. D2 receptor availability in the striatal regions was assessed using [11C]raclopride-PET. Treatment with both CGS21680 and KW6002 prevented a decrease in sucrose preference and decreased locomotor activity after social defeat. Both drugs decreased D2 receptor availability in the striatum, in particular in caudate-putamen. A2AR-antagonist treatment also decreased it D2 receptor availability in the nucleus-accumbens. Our study showed that the treatment with either an A2AR agonist or an A2AR antagonist prevented the development of depressive-like behavior, and reduced the availability of D2R in the striatum after exposure to RSD.</abstract><cop>Warsaw</cop><pub>Polish Academy of Sciences</pub></addata></record> |
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subjects | Adenosine Agonists Anxiety Availability Caudate-putamen Dopamine Dopamine D2 receptors Exposure Field tests Hedonic response Locomotor activity Neostriatum Nucleus accumbens Phenotypes Putamen Raclopride Receptors Social interactions Sucrose |
title | INFLUENCE OF A2A TREATMENT ON DEPRESSIVE‑LIKE BEHAVIOR AND D2‑RECEPTOR AVAILABILITY IN RATS EXPOSED TO REPEATED SOCIAL DEFEAT |
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