Posttraining activation of CB1 cannabinoid receptors in the CA1 region of the dorsal hippocampus impairs object recognition long-term memory
Evidence indicates that brain endocannabinoids are involved in memory processing. However, the participation of CB1 and CB2 cannabinoid receptors in recognition memory has not been yet conclusively determined. Therefore, we evaluated the effect of the posttraining activation of hippocampal cannabino...
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description | Evidence indicates that brain endocannabinoids are involved in memory processing. However, the participation of CB1 and CB2 cannabinoid receptors in recognition memory has not been yet conclusively determined. Therefore, we evaluated the effect of the posttraining activation of hippocampal cannabinoid receptors on the consolidation of object recognition memory. Rats with infusion cannulae stereotaxically aimed to the CA1 region of the dorsal hippocampus were trained in an object recognition learning task involving exposure to two different stimulus objects. Memory retention was assessed at different times after training. In the test sessions, one of the objects presented during training was replaced by a novel one. When infused in the CA1 region immediately after training, the non-selective cannabinoid receptor agonist WIN-55,212-2 and the endocannabinoid membrane transporter inhibitor VDM-11 blocked long-term memory retention in a dose-dependent manner without affecting short-term memory, exploratory behavior, anxiety state or the functionality of the hippocampus. The amnesic effect of WIN-55,212-2 and VDM-11 was not due to state-dependency and was completely reversed by co-infusion of the CB1 receptor antagonist AM-251 and mimicked by the CB1 receptor agonist ACEA but not by the CB2 receptor agonists JWH-015 and palmitoylethanolamide. Our data indicate that activation of hippocampal CB1 receptors early after training hampers consolidation of object recognition memory. |
doi_str_mv | 10.1016/j.nlm.2008.04.009 |
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However, the participation of CB1 and CB2 cannabinoid receptors in recognition memory has not been yet conclusively determined. Therefore, we evaluated the effect of the posttraining activation of hippocampal cannabinoid receptors on the consolidation of object recognition memory. Rats with infusion cannulae stereotaxically aimed to the CA1 region of the dorsal hippocampus were trained in an object recognition learning task involving exposure to two different stimulus objects. Memory retention was assessed at different times after training. In the test sessions, one of the objects presented during training was replaced by a novel one. When infused in the CA1 region immediately after training, the non-selective cannabinoid receptor agonist WIN-55,212-2 and the endocannabinoid membrane transporter inhibitor VDM-11 blocked long-term memory retention in a dose-dependent manner without affecting short-term memory, exploratory behavior, anxiety state or the functionality of the hippocampus. The amnesic effect of WIN-55,212-2 and VDM-11 was not due to state-dependency and was completely reversed by co-infusion of the CB1 receptor antagonist AM-251 and mimicked by the CB1 receptor agonist ACEA but not by the CB2 receptor agonists JWH-015 and palmitoylethanolamide. Our data indicate that activation of hippocampal CB1 receptors early after training hampers consolidation of object recognition memory.</description><identifier>ISSN: 1074-7427</identifier><identifier>EISSN: 1095-9564</identifier><identifier>DOI: 10.1016/j.nlm.2008.04.009</identifier><identifier>PMID: 18524639</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>ACEA ; AM251 ; Animals ; Arachidonic Acids - pharmacology ; Avoidance Learning - drug effects ; Avoidance Learning - physiology ; Behavioral psychophysiology ; Benzoxazines - pharmacology ; Biological and medical sciences ; Cannabinoids ; CB1 ; CB2 ; Consolidation ; Dominance, Cerebral - drug effects ; Dominance, Cerebral - physiology ; Dose-Response Relationship, Drug ; Electroshock ; Escape Reaction - drug effects ; Escape Reaction - physiology ; Exploratory Behavior - drug effects ; Exploratory Behavior - physiology ; Fear - drug effects ; Fear - physiology ; Fundamental and applied biological sciences. Psychology ; Hippocampus ; Hippocampus - drug effects ; Hippocampus - physiology ; Inhibitor drugs ; JWH-015 ; Learning ; Male ; Maze Learning - drug effects ; Maze Learning - physiology ; Memory ; Memory, Short-Term - drug effects ; Memory, Short-Term - physiology ; Morpholines - pharmacology ; Motor Activity - drug effects ; Motor Activity - physiology ; Naphthalenes - pharmacology ; Neurology ; Object recognition memory ; Palmitoylethanolamide ; Pattern Recognition, Visual - drug effects ; Pattern Recognition, Visual - physiology ; Psychology. Psychoanalysis. Psychiatry ; Psychology. Psychophysiology ; Rats ; Rats, Wistar ; Receptor, Cannabinoid, CB1 - agonists ; Receptor, Cannabinoid, CB1 - physiology ; Retention, Psychology - drug effects ; Retention, Psychology - physiology ; Rodents ; VDM-11 ; WIN-55,212-2</subject><ispartof>Neurobiology of learning and memory, 2008-09, Vol.90 (2), p.374-381</ispartof><rights>2008 Elsevier Inc.</rights><rights>2008 INIST-CNRS</rights><rights>Copyright © 2008 Elsevier B.V. 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However, the participation of CB1 and CB2 cannabinoid receptors in recognition memory has not been yet conclusively determined. Therefore, we evaluated the effect of the posttraining activation of hippocampal cannabinoid receptors on the consolidation of object recognition memory. Rats with infusion cannulae stereotaxically aimed to the CA1 region of the dorsal hippocampus were trained in an object recognition learning task involving exposure to two different stimulus objects. Memory retention was assessed at different times after training. In the test sessions, one of the objects presented during training was replaced by a novel one. When infused in the CA1 region immediately after training, the non-selective cannabinoid receptor agonist WIN-55,212-2 and the endocannabinoid membrane transporter inhibitor VDM-11 blocked long-term memory retention in a dose-dependent manner without affecting short-term memory, exploratory behavior, anxiety state or the functionality of the hippocampus. The amnesic effect of WIN-55,212-2 and VDM-11 was not due to state-dependency and was completely reversed by co-infusion of the CB1 receptor antagonist AM-251 and mimicked by the CB1 receptor agonist ACEA but not by the CB2 receptor agonists JWH-015 and palmitoylethanolamide. Our data indicate that activation of hippocampal CB1 receptors early after training hampers consolidation of object recognition memory.</description><subject>ACEA</subject><subject>AM251</subject><subject>Animals</subject><subject>Arachidonic Acids - pharmacology</subject><subject>Avoidance Learning - drug effects</subject><subject>Avoidance Learning - physiology</subject><subject>Behavioral psychophysiology</subject><subject>Benzoxazines - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cannabinoids</subject><subject>CB1</subject><subject>CB2</subject><subject>Consolidation</subject><subject>Dominance, Cerebral - drug effects</subject><subject>Dominance, Cerebral - physiology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Electroshock</subject><subject>Escape Reaction - drug effects</subject><subject>Escape Reaction - physiology</subject><subject>Exploratory Behavior - drug effects</subject><subject>Exploratory Behavior - physiology</subject><subject>Fear - drug effects</subject><subject>Fear - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - physiology</subject><subject>Inhibitor drugs</subject><subject>JWH-015</subject><subject>Learning</subject><subject>Male</subject><subject>Maze Learning - drug effects</subject><subject>Maze Learning - physiology</subject><subject>Memory</subject><subject>Memory, Short-Term - drug effects</subject><subject>Memory, Short-Term - physiology</subject><subject>Morpholines - pharmacology</subject><subject>Motor Activity - drug effects</subject><subject>Motor Activity - physiology</subject><subject>Naphthalenes - pharmacology</subject><subject>Neurology</subject><subject>Object recognition memory</subject><subject>Palmitoylethanolamide</subject><subject>Pattern Recognition, Visual - drug effects</subject><subject>Pattern Recognition, Visual - physiology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychology. Psychophysiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptor, Cannabinoid, CB1 - agonists</subject><subject>Receptor, Cannabinoid, CB1 - physiology</subject><subject>Retention, Psychology - drug effects</subject><subject>Retention, Psychology - physiology</subject><subject>Rodents</subject><subject>VDM-11</subject><subject>WIN-55,212-2</subject><issn>1074-7427</issn><issn>1095-9564</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc-O1SAUxhujccbRB3BjiInuej1ASyGuxhv_JZPoQteEAr1D00IFOsm8gw8t9TaauHAFOfy-7xzOV1XPMRwwYPZmPPhpPhAAfoDmACAeVJcYRFuLljUPt3vX1F1DuovqSUojAMat4I-rC8xb0jAqLqufX0PKOSrnnT8hpbO7U9kFj8KAju8w0sp71TsfnEHRarvkEBNyHuVbi47XuBRPO75VTHlVE7p1yxK0mpe1sPOiXNGEfrQ6bybh5N3vHlPwpzrbOKPZziHeP60eDWpK9tl-XlXfP7z_dvxU33z5-Pl4fVPrFtpcKzIo0hnom5YPhgprrIJeWWI0ETCAYErQFg90oL2hCrMOCAPW97jnxuqOXlWvz75LDD9Wm7KcXdJ2mpS3YU2SAOcd5aKAL_8Bx7BGX2aThDKCOet4gfAZ0jGkFO0gl-hmFe8lBrnlJEdZcpJbThIaWXIqmhe78drP1vxV7MEU4NUOqKTVNETltUt_OAIMM9ptX3l75mzZ152zUSbtrNfWuLLpLE1w_xnjF1drsq0</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Clarke, Julia R.</creator><creator>Rossato, Janine I.</creator><creator>Monteiro, Siomara</creator><creator>Bevilaqua, Lia R.M.</creator><creator>Izquierdo, Iván</creator><creator>Cammarota, Martín</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier BV</general><scope>IQODW</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>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20080901</creationdate><title>Posttraining activation of CB1 cannabinoid receptors in the CA1 region of the dorsal hippocampus impairs object recognition long-term memory</title><author>Clarke, Julia R. ; Rossato, Janine I. ; Monteiro, Siomara ; Bevilaqua, Lia R.M. ; Izquierdo, Iván ; Cammarota, Martín</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-a2fa27d0b458fd39edea0bae2dc290f096a9351f3f3bd3a16702606bb1b8dec73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>ACEA</topic><topic>AM251</topic><topic>Animals</topic><topic>Arachidonic Acids - pharmacology</topic><topic>Avoidance Learning - drug effects</topic><topic>Avoidance Learning - physiology</topic><topic>Behavioral psychophysiology</topic><topic>Benzoxazines - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cannabinoids</topic><topic>CB1</topic><topic>CB2</topic><topic>Consolidation</topic><topic>Dominance, Cerebral - drug effects</topic><topic>Dominance, Cerebral - physiology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Electroshock</topic><topic>Escape Reaction - drug effects</topic><topic>Escape Reaction - physiology</topic><topic>Exploratory Behavior - drug effects</topic><topic>Exploratory Behavior - physiology</topic><topic>Fear - drug effects</topic><topic>Fear - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hippocampus</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - physiology</topic><topic>Inhibitor drugs</topic><topic>JWH-015</topic><topic>Learning</topic><topic>Male</topic><topic>Maze Learning - drug effects</topic><topic>Maze Learning - physiology</topic><topic>Memory</topic><topic>Memory, Short-Term - drug effects</topic><topic>Memory, Short-Term - physiology</topic><topic>Morpholines - pharmacology</topic><topic>Motor Activity - drug effects</topic><topic>Motor Activity - physiology</topic><topic>Naphthalenes - pharmacology</topic><topic>Neurology</topic><topic>Object recognition memory</topic><topic>Palmitoylethanolamide</topic><topic>Pattern Recognition, Visual - drug effects</topic><topic>Pattern Recognition, Visual - physiology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychology. Psychophysiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptor, Cannabinoid, CB1 - agonists</topic><topic>Receptor, Cannabinoid, CB1 - physiology</topic><topic>Retention, Psychology - drug effects</topic><topic>Retention, Psychology - physiology</topic><topic>Rodents</topic><topic>VDM-11</topic><topic>WIN-55,212-2</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Clarke, Julia R.</creatorcontrib><creatorcontrib>Rossato, Janine I.</creatorcontrib><creatorcontrib>Monteiro, Siomara</creatorcontrib><creatorcontrib>Bevilaqua, Lia R.M.</creatorcontrib><creatorcontrib>Izquierdo, Iván</creatorcontrib><creatorcontrib>Cammarota, Martín</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Neurobiology of learning and memory</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clarke, Julia R.</au><au>Rossato, Janine I.</au><au>Monteiro, Siomara</au><au>Bevilaqua, Lia R.M.</au><au>Izquierdo, Iván</au><au>Cammarota, Martín</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Posttraining activation of CB1 cannabinoid receptors in the CA1 region of the dorsal hippocampus impairs object recognition long-term memory</atitle><jtitle>Neurobiology of learning and memory</jtitle><addtitle>Neurobiol Learn Mem</addtitle><date>2008-09-01</date><risdate>2008</risdate><volume>90</volume><issue>2</issue><spage>374</spage><epage>381</epage><pages>374-381</pages><issn>1074-7427</issn><eissn>1095-9564</eissn><abstract>Evidence indicates that brain endocannabinoids are involved in memory processing. However, the participation of CB1 and CB2 cannabinoid receptors in recognition memory has not been yet conclusively determined. Therefore, we evaluated the effect of the posttraining activation of hippocampal cannabinoid receptors on the consolidation of object recognition memory. Rats with infusion cannulae stereotaxically aimed to the CA1 region of the dorsal hippocampus were trained in an object recognition learning task involving exposure to two different stimulus objects. Memory retention was assessed at different times after training. In the test sessions, one of the objects presented during training was replaced by a novel one. When infused in the CA1 region immediately after training, the non-selective cannabinoid receptor agonist WIN-55,212-2 and the endocannabinoid membrane transporter inhibitor VDM-11 blocked long-term memory retention in a dose-dependent manner without affecting short-term memory, exploratory behavior, anxiety state or the functionality of the hippocampus. The amnesic effect of WIN-55,212-2 and VDM-11 was not due to state-dependency and was completely reversed by co-infusion of the CB1 receptor antagonist AM-251 and mimicked by the CB1 receptor agonist ACEA but not by the CB2 receptor agonists JWH-015 and palmitoylethanolamide. Our data indicate that activation of hippocampal CB1 receptors early after training hampers consolidation of object recognition memory.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>18524639</pmid><doi>10.1016/j.nlm.2008.04.009</doi><tpages>8</tpages></addata></record> |
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subjects | ACEA AM251 Animals Arachidonic Acids - pharmacology Avoidance Learning - drug effects Avoidance Learning - physiology Behavioral psychophysiology Benzoxazines - pharmacology Biological and medical sciences Cannabinoids CB1 CB2 Consolidation Dominance, Cerebral - drug effects Dominance, Cerebral - physiology Dose-Response Relationship, Drug Electroshock Escape Reaction - drug effects Escape Reaction - physiology Exploratory Behavior - drug effects Exploratory Behavior - physiology Fear - drug effects Fear - physiology Fundamental and applied biological sciences. Psychology Hippocampus Hippocampus - drug effects Hippocampus - physiology Inhibitor drugs JWH-015 Learning Male Maze Learning - drug effects Maze Learning - physiology Memory Memory, Short-Term - drug effects Memory, Short-Term - physiology Morpholines - pharmacology Motor Activity - drug effects Motor Activity - physiology Naphthalenes - pharmacology Neurology Object recognition memory Palmitoylethanolamide Pattern Recognition, Visual - drug effects Pattern Recognition, Visual - physiology Psychology. Psychoanalysis. Psychiatry Psychology. Psychophysiology Rats Rats, Wistar Receptor, Cannabinoid, CB1 - agonists Receptor, Cannabinoid, CB1 - physiology Retention, Psychology - drug effects Retention, Psychology - physiology Rodents VDM-11 WIN-55,212-2 |
title | Posttraining activation of CB1 cannabinoid receptors in the CA1 region of the dorsal hippocampus impairs object recognition long-term memory |
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