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Possible involvement of μ-opioid receptors in effect of lithium on inhibitory avoidance response in mice
In the present study, effects of intracerebroventricular (i.c.v.) injections of μ-opioid receptor agonist and antagonist on lithium state-dependency were investigated. For memory assessment, a one-trial step-down inhibitory avoidance task was used in adult male NMRI mice. Intraperitoneal (i.p.) admi...
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Published in: | Journal of psychopharmacology (Oxford) 2008-11, Vol.22 (8), p.865-871 |
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description | In the present study, effects of intracerebroventricular (i.c.v.) injections of μ-opioid receptor agonist and antagonist on lithium state-dependency were investigated. For memory assessment, a one-trial step-down inhibitory avoidance task was used in adult male NMRI mice. Intraperitoneal (i.p.) administration of lithium (10 mg/kg) after training impaired memory when retrieval was tested 24 h later. The memory impairment was reversed by pretest administration of the same dose of lithium, suggesting state-dependency induced by lithium. In addition, i.c.v. administration of both lithium (2 and 4 μg/mouse, i.c.v.) and morphine (3 and 6 μg/mouse, i.c.v.) before the test reversed memory impairment induced by post-training lithium (10 mg/kg, i.p.). On the other hand, pretest administration of naloxone (1 and 2 mg/kg) which had no effects alone on inhibitory avoidance response, prevented the improving effects of both morphine (3 μg/mouse, i.c.v.) and lithium (2 μg/mouse, i.c.v.) on memory retrieval. The results suggest that the μ-opioid receptors in the central nervous system may be involved in the retrieval of lithium state-dependent learning. |
doi_str_mv | 10.1177/0269881107083848 |
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For memory assessment, a one-trial step-down inhibitory avoidance task was used in adult male NMRI mice. Intraperitoneal (i.p.) administration of lithium (10 mg/kg) after training impaired memory when retrieval was tested 24 h later. The memory impairment was reversed by pretest administration of the same dose of lithium, suggesting state-dependency induced by lithium. In addition, i.c.v. administration of both lithium (2 and 4 μg/mouse, i.c.v.) and morphine (3 and 6 μg/mouse, i.c.v.) before the test reversed memory impairment induced by post-training lithium (10 mg/kg, i.p.). On the other hand, pretest administration of naloxone (1 and 2 mg/kg) which had no effects alone on inhibitory avoidance response, prevented the improving effects of both morphine (3 μg/mouse, i.c.v.) and lithium (2 μg/mouse, i.c.v.) on memory retrieval. The results suggest that the μ-opioid receptors in the central nervous system may be involved in the retrieval of lithium state-dependent learning.</description><identifier>ISSN: 0269-8811</identifier><identifier>EISSN: 1461-7285</identifier><identifier>DOI: 10.1177/0269881107083848</identifier><identifier>PMID: 18208927</identifier><identifier>CODEN: JOPSEQ</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Animals ; Antimanic Agents - pharmacology ; Avoidance Learning - drug effects ; Biological and medical sciences ; Cognitive ability ; Lithium ; Lithium Chloride - pharmacology ; Male ; Medical sciences ; Memory ; Memory Disorders - chemically induced ; Mice ; Morphine - pharmacology ; Naloxone - pharmacology ; Narcotics ; Neuropharmacology ; Pharmacology. Drug treatments ; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer ; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) ; Psychology. Psychoanalysis. Psychiatry ; Psychopharmacology ; Receptors, Opioid, mu - physiology</subject><ispartof>Journal of psychopharmacology (Oxford), 2008-11, Vol.22 (8), p.865-871</ispartof><rights>2009 INIST-CNRS</rights><rights>Copyright Sage Publications Ltd. Nov 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-e5d69d7dee9b1dd69820928bf4f9e8b7e6aefb7ea825f3f389086f296ca87c8a3</citedby><cites>FETCH-LOGICAL-c392t-e5d69d7dee9b1dd69820928bf4f9e8b7e6aefb7ea825f3f389086f296ca87c8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904,79110</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20838726$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18208927$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zarrindast, M-R.</creatorcontrib><creatorcontrib>Lahmi, A.</creatorcontrib><creatorcontrib>Ahamadi, S.</creatorcontrib><title>Possible involvement of μ-opioid receptors in effect of lithium on inhibitory avoidance response in mice</title><title>Journal of psychopharmacology (Oxford)</title><addtitle>J Psychopharmacol</addtitle><description>In the present study, effects of intracerebroventricular (i.c.v.) injections of μ-opioid receptor agonist and antagonist on lithium state-dependency were investigated. For memory assessment, a one-trial step-down inhibitory avoidance task was used in adult male NMRI mice. Intraperitoneal (i.p.) administration of lithium (10 mg/kg) after training impaired memory when retrieval was tested 24 h later. The memory impairment was reversed by pretest administration of the same dose of lithium, suggesting state-dependency induced by lithium. In addition, i.c.v. administration of both lithium (2 and 4 μg/mouse, i.c.v.) and morphine (3 and 6 μg/mouse, i.c.v.) before the test reversed memory impairment induced by post-training lithium (10 mg/kg, i.p.). On the other hand, pretest administration of naloxone (1 and 2 mg/kg) which had no effects alone on inhibitory avoidance response, prevented the improving effects of both morphine (3 μg/mouse, i.c.v.) and lithium (2 μg/mouse, i.c.v.) on memory retrieval. The results suggest that the μ-opioid receptors in the central nervous system may be involved in the retrieval of lithium state-dependent learning.</description><subject>Animals</subject><subject>Antimanic Agents - pharmacology</subject><subject>Avoidance Learning - drug effects</subject><subject>Biological and medical sciences</subject><subject>Cognitive ability</subject><subject>Lithium</subject><subject>Lithium Chloride - pharmacology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Memory</subject><subject>Memory Disorders - chemically induced</subject><subject>Mice</subject><subject>Morphine - pharmacology</subject><subject>Naloxone - pharmacology</subject><subject>Narcotics</subject><subject>Neuropharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer</subject><subject>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopharmacology</subject><subject>Receptors, Opioid, mu - physiology</subject><issn>0269-8811</issn><issn>1461-7285</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kM1KAzEUhYMotlb3rmQQXI4mmWl-llL8g4IudD1kMjc2ZWYyJtNC381n8JnM2GJBcHVD7nfOvfcgdE7wNSGc32DKpBCEYI5FJnJxgMYkZyTlVEwP0Xhop0N_hE5CWGJMWM6mx2hEBMVCUj5G9sWFYMsaEtuuXb2GBto-cSb5-kxdZ52tEg8aut75EJEEjAH9A9S2X9hVk7g2_i9saSOySdQ6SlSrIcpC59owGCeN1XCKjoyqA5zt6gS93d-9zh7T-fPD0-x2nupM0j6FacVkxSsAWZIqvuOqkorS5EaCKDkwBSYWJejUZCYTEgtmqGRaCa6FyibocuvbefexgtAXS7fybRxZUEKzHDPOIoS3kPbxfg-m6LxtlN8UBBdDtMXfaKPkYue7Khuo9oJdlhG42gEqaFUbH2Ow4Zejgw-nw-x0ywX1Dvvl_h38DeoCkBc</recordid><startdate>20081101</startdate><enddate>20081101</enddate><creator>Zarrindast, M-R.</creator><creator>Lahmi, A.</creator><creator>Ahamadi, S.</creator><general>SAGE Publications</general><general>Sage Publications</general><general>Sage Publications Ltd</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>7TK</scope></search><sort><creationdate>20081101</creationdate><title>Possible involvement of μ-opioid receptors in effect of lithium on inhibitory avoidance response in mice</title><author>Zarrindast, M-R. ; Lahmi, A. ; Ahamadi, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-e5d69d7dee9b1dd69820928bf4f9e8b7e6aefb7ea825f3f389086f296ca87c8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Antimanic Agents - pharmacology</topic><topic>Avoidance Learning - drug effects</topic><topic>Biological and medical sciences</topic><topic>Cognitive ability</topic><topic>Lithium</topic><topic>Lithium Chloride - pharmacology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Memory</topic><topic>Memory Disorders - chemically induced</topic><topic>Mice</topic><topic>Morphine - pharmacology</topic><topic>Naloxone - pharmacology</topic><topic>Narcotics</topic><topic>Neuropharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer</topic><topic>Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopharmacology</topic><topic>Receptors, Opioid, mu - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zarrindast, M-R.</creatorcontrib><creatorcontrib>Lahmi, A.</creatorcontrib><creatorcontrib>Ahamadi, S.</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>Neurosciences Abstracts</collection><jtitle>Journal of psychopharmacology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zarrindast, M-R.</au><au>Lahmi, A.</au><au>Ahamadi, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Possible involvement of μ-opioid receptors in effect of lithium on inhibitory avoidance response in mice</atitle><jtitle>Journal of psychopharmacology (Oxford)</jtitle><addtitle>J Psychopharmacol</addtitle><date>2008-11-01</date><risdate>2008</risdate><volume>22</volume><issue>8</issue><spage>865</spage><epage>871</epage><pages>865-871</pages><issn>0269-8811</issn><eissn>1461-7285</eissn><coden>JOPSEQ</coden><abstract>In the present study, effects of intracerebroventricular (i.c.v.) injections of μ-opioid receptor agonist and antagonist on lithium state-dependency were investigated. For memory assessment, a one-trial step-down inhibitory avoidance task was used in adult male NMRI mice. Intraperitoneal (i.p.) administration of lithium (10 mg/kg) after training impaired memory when retrieval was tested 24 h later. The memory impairment was reversed by pretest administration of the same dose of lithium, suggesting state-dependency induced by lithium. In addition, i.c.v. administration of both lithium (2 and 4 μg/mouse, i.c.v.) and morphine (3 and 6 μg/mouse, i.c.v.) before the test reversed memory impairment induced by post-training lithium (10 mg/kg, i.p.). On the other hand, pretest administration of naloxone (1 and 2 mg/kg) which had no effects alone on inhibitory avoidance response, prevented the improving effects of both morphine (3 μg/mouse, i.c.v.) and lithium (2 μg/mouse, i.c.v.) on memory retrieval. The results suggest that the μ-opioid receptors in the central nervous system may be involved in the retrieval of lithium state-dependent learning.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>18208927</pmid><doi>10.1177/0269881107083848</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Antimanic Agents - pharmacology Avoidance Learning - drug effects Biological and medical sciences Cognitive ability Lithium Lithium Chloride - pharmacology Male Medical sciences Memory Memory Disorders - chemically induced Mice Morphine - pharmacology Naloxone - pharmacology Narcotics Neuropharmacology Pharmacology. Drug treatments Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) Psychology. Psychoanalysis. Psychiatry Psychopharmacology Receptors, Opioid, mu - physiology |
title | Possible involvement of μ-opioid receptors in effect of lithium on inhibitory avoidance response in mice |
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