Incentive salience of cocaine across the postpartum period of the female rat
Rationale–Objectives Our prior conditioned place preference (CPP) work demonstrates that late (day16) postpartum female rats consistently prefer cocaine- over pup-associated chambers, whereas far fewer early postpartum (day8) females prefer the cocaine-associated chamber. The present study examines...
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description | Rationale–Objectives
Our prior conditioned place preference (CPP) work demonstrates that late (day16) postpartum female rats consistently prefer cocaine- over pup-associated chambers, whereas far fewer early postpartum (day8) females prefer the cocaine-associated chamber. The present study examines early and late postpartum females’ preference for a cocaine-associated chamber when contrasted with a chamber associated with saline (rather than pups).
Materials and methods
Postpartum females were tested for conditioned preference for chambers associated with cocaine (10 mg/kg subcutaneous (SC) or 0.5, 5, 10, or 20 mg/kg intraperitoneal (IP) injections) versus saline; preferences of virgin female and male rats for select cocaine stimuli (10mg/kg SC or IP) were also tested. Locomotion was recorded during CPP conditioning and testing.
Results
Early and late postpartum females expressed strikingly similar preference for the cocaine-associated chamber across all administration routes and doses. IP cocaine produced an orderly, inverted U-shaped dose-preference curve, with preference peaking at the 5 mg/kg dose (83% of females). While many postpartum females preferred 10mg/kg cocaine administered either SC or IP, both virgin females and males expressed strong aversion to SC cocaine and, while virgin females strongly preferred IP cocaine, males remained relatively indifferent. Across 10mg/kg IP cocaine-conditioning sessions, locomotor sensitization occurred exclusively in cocaine- but not saline-preferring postpartum females. Locomotor rate was lower in preferred versus nonpreferred chambers at CPP test.
Conclusions
Early and late postpartum females may be equally and uniquely susceptible to sampling and/or abuse of modestly salient doses of cocaine (10mg/kg SC; 5mg/kg IP) compared to virgin females and/or males. |
doi_str_mv | 10.1007/s00213-008-1140-9 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2574577</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20821080</sourcerecordid><originalsourceid>FETCH-LOGICAL-c528t-951b138912241d452693dd611e1579fe623077efd30d8b354228f163ea34c7383</originalsourceid><addsrcrecordid>eNp1kU1r3DAQhkVpaLbb_oBeiik0Nzcz-rDkSyGEfgQWcknPQmuPEwXbciU7kH9fubskbaG6CDHPvDOvXsbeIXxCAH2eADiKEsCUiBLK-gXboBS85KD5S7YBEKIUqMwpe53SPeQjjXzFTtFIDVVdbdjuamxonP0DFcn1nvKrCF3RhMb5kQrXxJBSMd9RMYU0Ty7Oy1BMFH1oV24tdDS4noro5jfspHN9orfHe8t-fP1yc_m93F1_u7q82JWN4mYua4V7FKZGziW2UvGqFm1bIRIqXXdUcQFaU9cKaM1eKMm56bAS5IRstDBiyz4fdKdlP1C7Goiut1P0g4uPNjhv_66M_s7ehgfLlZZK6yxwdhSI4edCabaDTw31vRspLMlyMBzBQAY__APehyWO2ZzlaGqldF52y_AA_f6sSN3TJgh2DcoegrI5KLsGZevc8_5PC88dx2Qy8PEIuNS4votubHx64jhIXSGXmeMHLuXSeEvxecP_T_8FfgCprg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>218955762</pqid></control><display><type>article</type><title>Incentive salience of cocaine across the postpartum period of the female rat</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Seip, Katharine M. ; Pereira, Mariana ; Wansaw, Michael P. ; Reiss, Jenny I. ; Dziopa, Eugenia I. ; Morrell, Joan I.</creator><creatorcontrib>Seip, Katharine M. ; Pereira, Mariana ; Wansaw, Michael P. ; Reiss, Jenny I. ; Dziopa, Eugenia I. ; Morrell, Joan I.</creatorcontrib><description>Rationale–Objectives
Our prior conditioned place preference (CPP) work demonstrates that late (day16) postpartum female rats consistently prefer cocaine- over pup-associated chambers, whereas far fewer early postpartum (day8) females prefer the cocaine-associated chamber. The present study examines early and late postpartum females’ preference for a cocaine-associated chamber when contrasted with a chamber associated with saline (rather than pups).
Materials and methods
Postpartum females were tested for conditioned preference for chambers associated with cocaine (10 mg/kg subcutaneous (SC) or 0.5, 5, 10, or 20 mg/kg intraperitoneal (IP) injections) versus saline; preferences of virgin female and male rats for select cocaine stimuli (10mg/kg SC or IP) were also tested. Locomotion was recorded during CPP conditioning and testing.
Results
Early and late postpartum females expressed strikingly similar preference for the cocaine-associated chamber across all administration routes and doses. IP cocaine produced an orderly, inverted U-shaped dose-preference curve, with preference peaking at the 5 mg/kg dose (83% of females). While many postpartum females preferred 10mg/kg cocaine administered either SC or IP, both virgin females and males expressed strong aversion to SC cocaine and, while virgin females strongly preferred IP cocaine, males remained relatively indifferent. Across 10mg/kg IP cocaine-conditioning sessions, locomotor sensitization occurred exclusively in cocaine- but not saline-preferring postpartum females. Locomotor rate was lower in preferred versus nonpreferred chambers at CPP test.
Conclusions
Early and late postpartum females may be equally and uniquely susceptible to sampling and/or abuse of modestly salient doses of cocaine (10mg/kg SC; 5mg/kg IP) compared to virgin females and/or males.</description><identifier>ISSN: 0033-3158</identifier><identifier>EISSN: 1432-2072</identifier><identifier>DOI: 10.1007/s00213-008-1140-9</identifier><identifier>PMID: 18470696</identifier><identifier>CODEN: PSYPAG</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Animal behavior ; Animals ; Biological and medical sciences ; Biomedical and Life Sciences ; Biomedicine ; Choice Behavior - drug effects ; Cocaine ; Cocaine - administration & dosage ; Conditioning, Classical ; Dose-Response Relationship, Drug ; Female ; Females ; Injections, Intraperitoneal ; Injections, Subcutaneous ; Male ; Maternal Behavior - drug effects ; Medical sciences ; Motivation ; Motor Activity - drug effects ; Neuropharmacology ; Neurosciences ; Original Investigation ; Pharmacology. Drug treatments ; Pharmacology/Toxicology ; Postpartum period ; Pregnancy ; Pregnancy, Animal ; Psychiatry ; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer ; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) ; Psychology. Psychoanalysis. Psychiatry ; Psychopharmacology ; Rats ; Rats, Sprague-Dawley ; Rodents ; Sex Factors ; Social Environment</subject><ispartof>Psychopharmacologia, 2008-07, Vol.199 (1), p.119-130</ispartof><rights>Springer-Verlag 2008</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-951b138912241d452693dd611e1579fe623077efd30d8b354228f163ea34c7383</citedby><cites>FETCH-LOGICAL-c528t-951b138912241d452693dd611e1579fe623077efd30d8b354228f163ea34c7383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00213-008-1140-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00213-008-1140-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20476124$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18470696$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Seip, Katharine M.</creatorcontrib><creatorcontrib>Pereira, Mariana</creatorcontrib><creatorcontrib>Wansaw, Michael P.</creatorcontrib><creatorcontrib>Reiss, Jenny I.</creatorcontrib><creatorcontrib>Dziopa, Eugenia I.</creatorcontrib><creatorcontrib>Morrell, Joan I.</creatorcontrib><title>Incentive salience of cocaine across the postpartum period of the female rat</title><title>Psychopharmacologia</title><addtitle>Psychopharmacology</addtitle><addtitle>Psychopharmacology (Berl)</addtitle><description>Rationale–Objectives
Our prior conditioned place preference (CPP) work demonstrates that late (day16) postpartum female rats consistently prefer cocaine- over pup-associated chambers, whereas far fewer early postpartum (day8) females prefer the cocaine-associated chamber. The present study examines early and late postpartum females’ preference for a cocaine-associated chamber when contrasted with a chamber associated with saline (rather than pups).
Materials and methods
Postpartum females were tested for conditioned preference for chambers associated with cocaine (10 mg/kg subcutaneous (SC) or 0.5, 5, 10, or 20 mg/kg intraperitoneal (IP) injections) versus saline; preferences of virgin female and male rats for select cocaine stimuli (10mg/kg SC or IP) were also tested. Locomotion was recorded during CPP conditioning and testing.
Results
Early and late postpartum females expressed strikingly similar preference for the cocaine-associated chamber across all administration routes and doses. IP cocaine produced an orderly, inverted U-shaped dose-preference curve, with preference peaking at the 5 mg/kg dose (83% of females). While many postpartum females preferred 10mg/kg cocaine administered either SC or IP, both virgin females and males expressed strong aversion to SC cocaine and, while virgin females strongly preferred IP cocaine, males remained relatively indifferent. Across 10mg/kg IP cocaine-conditioning sessions, locomotor sensitization occurred exclusively in cocaine- but not saline-preferring postpartum females. Locomotor rate was lower in preferred versus nonpreferred chambers at CPP test.
Conclusions
Early and late postpartum females may be equally and uniquely susceptible to sampling and/or abuse of modestly salient doses of cocaine (10mg/kg SC; 5mg/kg IP) compared to virgin females and/or males.</description><subject>Animal behavior</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Choice Behavior - drug effects</subject><subject>Cocaine</subject><subject>Cocaine - administration & dosage</subject><subject>Conditioning, Classical</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Females</subject><subject>Injections, Intraperitoneal</subject><subject>Injections, Subcutaneous</subject><subject>Male</subject><subject>Maternal Behavior - drug effects</subject><subject>Medical sciences</subject><subject>Motivation</subject><subject>Motor Activity - drug effects</subject><subject>Neuropharmacology</subject><subject>Neurosciences</subject><subject>Original Investigation</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacology/Toxicology</subject><subject>Postpartum period</subject><subject>Pregnancy</subject><subject>Pregnancy, Animal</subject><subject>Psychiatry</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>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Rodents</subject><subject>Sex Factors</subject><subject>Social Environment</subject><issn>0033-3158</issn><issn>1432-2072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kU1r3DAQhkVpaLbb_oBeiik0Nzcz-rDkSyGEfgQWcknPQmuPEwXbciU7kH9fubskbaG6CDHPvDOvXsbeIXxCAH2eADiKEsCUiBLK-gXboBS85KD5S7YBEKIUqMwpe53SPeQjjXzFTtFIDVVdbdjuamxonP0DFcn1nvKrCF3RhMb5kQrXxJBSMd9RMYU0Ty7Oy1BMFH1oV24tdDS4noro5jfspHN9orfHe8t-fP1yc_m93F1_u7q82JWN4mYua4V7FKZGziW2UvGqFm1bIRIqXXdUcQFaU9cKaM1eKMm56bAS5IRstDBiyz4fdKdlP1C7Goiut1P0g4uPNjhv_66M_s7ehgfLlZZK6yxwdhSI4edCabaDTw31vRspLMlyMBzBQAY__APehyWO2ZzlaGqldF52y_AA_f6sSN3TJgh2DcoegrI5KLsGZevc8_5PC88dx2Qy8PEIuNS4votubHx64jhIXSGXmeMHLuXSeEvxecP_T_8FfgCprg</recordid><startdate>20080701</startdate><enddate>20080701</enddate><creator>Seip, Katharine M.</creator><creator>Pereira, Mariana</creator><creator>Wansaw, Michael P.</creator><creator>Reiss, Jenny I.</creator><creator>Dziopa, Eugenia I.</creator><creator>Morrell, Joan I.</creator><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7QG</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>20080701</creationdate><title>Incentive salience of cocaine across the postpartum period of the female rat</title><author>Seip, Katharine M. ; Pereira, Mariana ; Wansaw, Michael P. ; Reiss, Jenny I. ; Dziopa, Eugenia I. ; Morrell, Joan I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-951b138912241d452693dd611e1579fe623077efd30d8b354228f163ea34c7383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animal behavior</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Choice Behavior - drug effects</topic><topic>Cocaine</topic><topic>Cocaine - administration & dosage</topic><topic>Conditioning, Classical</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Females</topic><topic>Injections, Intraperitoneal</topic><topic>Injections, Subcutaneous</topic><topic>Male</topic><topic>Maternal Behavior - drug effects</topic><topic>Medical sciences</topic><topic>Motivation</topic><topic>Motor Activity - drug effects</topic><topic>Neuropharmacology</topic><topic>Neurosciences</topic><topic>Original Investigation</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacology/Toxicology</topic><topic>Postpartum period</topic><topic>Pregnancy</topic><topic>Pregnancy, Animal</topic><topic>Psychiatry</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>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Rodents</topic><topic>Sex Factors</topic><topic>Social Environment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seip, Katharine M.</creatorcontrib><creatorcontrib>Pereira, Mariana</creatorcontrib><creatorcontrib>Wansaw, Michael P.</creatorcontrib><creatorcontrib>Reiss, Jenny I.</creatorcontrib><creatorcontrib>Dziopa, Eugenia I.</creatorcontrib><creatorcontrib>Morrell, Joan I.</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>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Psychopharmacologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seip, Katharine M.</au><au>Pereira, Mariana</au><au>Wansaw, Michael P.</au><au>Reiss, Jenny I.</au><au>Dziopa, Eugenia I.</au><au>Morrell, Joan I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Incentive salience of cocaine across the postpartum period of the female rat</atitle><jtitle>Psychopharmacologia</jtitle><stitle>Psychopharmacology</stitle><addtitle>Psychopharmacology (Berl)</addtitle><date>2008-07-01</date><risdate>2008</risdate><volume>199</volume><issue>1</issue><spage>119</spage><epage>130</epage><pages>119-130</pages><issn>0033-3158</issn><eissn>1432-2072</eissn><coden>PSYPAG</coden><abstract>Rationale–Objectives
Our prior conditioned place preference (CPP) work demonstrates that late (day16) postpartum female rats consistently prefer cocaine- over pup-associated chambers, whereas far fewer early postpartum (day8) females prefer the cocaine-associated chamber. The present study examines early and late postpartum females’ preference for a cocaine-associated chamber when contrasted with a chamber associated with saline (rather than pups).
Materials and methods
Postpartum females were tested for conditioned preference for chambers associated with cocaine (10 mg/kg subcutaneous (SC) or 0.5, 5, 10, or 20 mg/kg intraperitoneal (IP) injections) versus saline; preferences of virgin female and male rats for select cocaine stimuli (10mg/kg SC or IP) were also tested. Locomotion was recorded during CPP conditioning and testing.
Results
Early and late postpartum females expressed strikingly similar preference for the cocaine-associated chamber across all administration routes and doses. IP cocaine produced an orderly, inverted U-shaped dose-preference curve, with preference peaking at the 5 mg/kg dose (83% of females). While many postpartum females preferred 10mg/kg cocaine administered either SC or IP, both virgin females and males expressed strong aversion to SC cocaine and, while virgin females strongly preferred IP cocaine, males remained relatively indifferent. Across 10mg/kg IP cocaine-conditioning sessions, locomotor sensitization occurred exclusively in cocaine- but not saline-preferring postpartum females. Locomotor rate was lower in preferred versus nonpreferred chambers at CPP test.
Conclusions
Early and late postpartum females may be equally and uniquely susceptible to sampling and/or abuse of modestly salient doses of cocaine (10mg/kg SC; 5mg/kg IP) compared to virgin females and/or males.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>18470696</pmid><doi>10.1007/s00213-008-1140-9</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal behavior Animals Biological and medical sciences Biomedical and Life Sciences Biomedicine Choice Behavior - drug effects Cocaine Cocaine - administration & dosage Conditioning, Classical Dose-Response Relationship, Drug Female Females Injections, Intraperitoneal Injections, Subcutaneous Male Maternal Behavior - drug effects Medical sciences Motivation Motor Activity - drug effects Neuropharmacology Neurosciences Original Investigation Pharmacology. Drug treatments Pharmacology/Toxicology Postpartum period Pregnancy Pregnancy, Animal Psychiatry Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease) Psychology. Psychoanalysis. Psychiatry Psychopharmacology Rats Rats, Sprague-Dawley Rodents Sex Factors Social Environment |
title | Incentive salience of cocaine across the postpartum period of the female rat |
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