GABA mechanisms in the pedunculopontine tegmental nucleus influence particular aspects of nicotine self-administration selectively in the rat
The pedunculopontine tegmental nucleus (PPTg) is part of the neuronal circuit activated by self-administered nicotine. The cholinergic neurons of the PPTg comprise a prominent projection to midbrain dopamine neurons. However, anatomical studies of Fos expression suggest that nicotine targets primari...
Gespeichert in:
Veröffentlicht in: | Psychopharmacologia 2001-11, Vol.158 (2), p.190-197 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 197 |
---|---|
container_issue | 2 |
container_start_page | 190 |
container_title | Psychopharmacologia |
container_volume | 158 |
creator | CORRIGALL, William A COEN, Kathleen M JIANHUA ZHANG ADAMSON, K. Laurel |
description | The pedunculopontine tegmental nucleus (PPTg) is part of the neuronal circuit activated by self-administered nicotine. The cholinergic neurons of the PPTg comprise a prominent projection to midbrain dopamine neurons. However, anatomical studies of Fos expression suggest that nicotine targets primarily non-cholinergic neurons in the PPTg, especially GABAergic and glutamatergic neurons.
The objective of these experiments was to examine the role of GABA manipulations in the PPTg on nicotine self-administration.
Rats trained to self-administer nicotine or cocaine intravenously were prepared with brain microcannulae directed to the PPTg. Intra-PPTg microinfusions of the GABA agonists muscimol (10-50 ng) and baclofen (30-60 ng) reduced nicotine self-administration maintained on a fixed-ratio schedule of reinforcement (30 microg/kg per infusion); self-administration of cocaine (0.3 mg/kg per infusion) under an identical schedule was not affected. Muscimol and baclofen were also examined after intra-PPTg microinfusion in animals trained to self-administer nicotine on a progressive-ratio schedule (10 and 30 microg/kg per infusion). Progressive-ratio responding was sensitive to pharmacological manipulations such as a change in the nicotine dose available for self-administration, or intra-PPTg microinfusion of the nicotinic antagonist dihydro-beta-erythroidine (30 microg). However, nicotine self-administration on a progressive-ratio schedule was not altered by intra-PPTg microinfusions of GABA agonists.
These data confirm that the PPTg is involved in nicotine self-administration, a conclusion that is independent of the schedule of reinforcement that is used. GABAergic mechanisms in the PPTg play a selective role in nicotine reinforcement compared to cocaine, and that role is restricted to the characteristics of reinforcement measured by fixed-ratio responding. |
doi_str_mv | 10.1007/s002130100869 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72274309</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18234848</sourcerecordid><originalsourceid>FETCH-LOGICAL-c378t-b9ac0b0c962560f1199f84827f6bff580e5cdf54c575f2e4ea98203a55abbe9e3</originalsourceid><addsrcrecordid>eNqF0U9vFCEUAHBibOxaPXo1kxi9TfuAYYHj2mg1aeKlnicM-7A0DDPyx6Qfwu8sa9c0epELBH68B-8R8orCOQWQFxmAUQ5trbb6CdnQgbOegWRPyQaA855ToU7J85zvoI1BDc_IKaUSGGi-IT-vdu933Yz21kSf59z52JVb7Fbc12hrWNYlFh-xK_htxlhM6GK1AetBulAx2oZNKr5hkzqTV7Qld4vrorfL76sZg-vNfvYtQ0mm-CUe9przPzDc_0nZTl6QE2dCxpfH-Yx8_fjh5vJTf_3l6vPl7rq3XKrST9pYmMDqLRNbcJRq7dSgmHTbyTmhAIXdOzFYIYVjOKDRigE3QphpQo38jLx7iLum5XvFXMbZZ4shmIhLzaNkTA68Feh_kCrGW0lVg2_-gXdLTbF9YuSt2lK3F8im-gdl05JzQjeuyc8m3Y8UxkM7x7_a2fzrY9Q6zbh_1Mf-NfD2CEy2JrhkovX50Q0gBRea_wK34Kmo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3117799827</pqid></control><display><type>article</type><title>GABA mechanisms in the pedunculopontine tegmental nucleus influence particular aspects of nicotine self-administration selectively in the rat</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>CORRIGALL, William A ; COEN, Kathleen M ; JIANHUA ZHANG ; ADAMSON, K. Laurel</creator><creatorcontrib>CORRIGALL, William A ; COEN, Kathleen M ; JIANHUA ZHANG ; ADAMSON, K. Laurel</creatorcontrib><description>The pedunculopontine tegmental nucleus (PPTg) is part of the neuronal circuit activated by self-administered nicotine. The cholinergic neurons of the PPTg comprise a prominent projection to midbrain dopamine neurons. However, anatomical studies of Fos expression suggest that nicotine targets primarily non-cholinergic neurons in the PPTg, especially GABAergic and glutamatergic neurons.
The objective of these experiments was to examine the role of GABA manipulations in the PPTg on nicotine self-administration.
Rats trained to self-administer nicotine or cocaine intravenously were prepared with brain microcannulae directed to the PPTg. Intra-PPTg microinfusions of the GABA agonists muscimol (10-50 ng) and baclofen (30-60 ng) reduced nicotine self-administration maintained on a fixed-ratio schedule of reinforcement (30 microg/kg per infusion); self-administration of cocaine (0.3 mg/kg per infusion) under an identical schedule was not affected. Muscimol and baclofen were also examined after intra-PPTg microinfusion in animals trained to self-administer nicotine on a progressive-ratio schedule (10 and 30 microg/kg per infusion). Progressive-ratio responding was sensitive to pharmacological manipulations such as a change in the nicotine dose available for self-administration, or intra-PPTg microinfusion of the nicotinic antagonist dihydro-beta-erythroidine (30 microg). However, nicotine self-administration on a progressive-ratio schedule was not altered by intra-PPTg microinfusions of GABA agonists.
These data confirm that the PPTg is involved in nicotine self-administration, a conclusion that is independent of the schedule of reinforcement that is used. GABAergic mechanisms in the PPTg play a selective role in nicotine reinforcement compared to cocaine, and that role is restricted to the characteristics of reinforcement measured by fixed-ratio responding.</description><identifier>ISSN: 0033-3158</identifier><identifier>EISSN: 1432-2072</identifier><identifier>DOI: 10.1007/s002130100869</identifier><identifier>PMID: 11702093</identifier><identifier>CODEN: PSYPAG</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Agonists ; Animals ; Baclofen ; Biological and medical sciences ; Brain Stem - drug effects ; Brain Stem - physiology ; Cocaine ; Cocaine - administration & dosage ; Dopamine Uptake Inhibitors - administration & dosage ; Dose-Response Relationship, Drug ; Drug self-administration ; GABA Agonists - pharmacology ; Glutamatergic transmission ; Male ; Medical sciences ; Mesencephalon ; Muscimol ; Neurons ; Nicotine ; Nicotine - administration & dosage ; Nicotinic Agonists - administration & dosage ; pedunculopontine nucleus ; Pedunculopontine tegmental nucleus ; Rats ; Rats, Long-Evans ; Reinforcement Schedule ; Reinforcement schedules ; Self Administration ; Tegmentum Mesencephali - drug effects ; Tegmentum Mesencephali - physiology ; Tobacco, tobacco smoking ; Toxicology ; γ-Aminobutyric acid</subject><ispartof>Psychopharmacologia, 2001-11, Vol.158 (2), p.190-197</ispartof><rights>2002 INIST-CNRS</rights><rights>Springer-Verlag 2001.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c378t-b9ac0b0c962560f1199f84827f6bff580e5cdf54c575f2e4ea98203a55abbe9e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14075359$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11702093$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CORRIGALL, William A</creatorcontrib><creatorcontrib>COEN, Kathleen M</creatorcontrib><creatorcontrib>JIANHUA ZHANG</creatorcontrib><creatorcontrib>ADAMSON, K. Laurel</creatorcontrib><title>GABA mechanisms in the pedunculopontine tegmental nucleus influence particular aspects of nicotine self-administration selectively in the rat</title><title>Psychopharmacologia</title><addtitle>Psychopharmacology (Berl)</addtitle><description>The pedunculopontine tegmental nucleus (PPTg) is part of the neuronal circuit activated by self-administered nicotine. The cholinergic neurons of the PPTg comprise a prominent projection to midbrain dopamine neurons. However, anatomical studies of Fos expression suggest that nicotine targets primarily non-cholinergic neurons in the PPTg, especially GABAergic and glutamatergic neurons.
The objective of these experiments was to examine the role of GABA manipulations in the PPTg on nicotine self-administration.
Rats trained to self-administer nicotine or cocaine intravenously were prepared with brain microcannulae directed to the PPTg. Intra-PPTg microinfusions of the GABA agonists muscimol (10-50 ng) and baclofen (30-60 ng) reduced nicotine self-administration maintained on a fixed-ratio schedule of reinforcement (30 microg/kg per infusion); self-administration of cocaine (0.3 mg/kg per infusion) under an identical schedule was not affected. Muscimol and baclofen were also examined after intra-PPTg microinfusion in animals trained to self-administer nicotine on a progressive-ratio schedule (10 and 30 microg/kg per infusion). Progressive-ratio responding was sensitive to pharmacological manipulations such as a change in the nicotine dose available for self-administration, or intra-PPTg microinfusion of the nicotinic antagonist dihydro-beta-erythroidine (30 microg). However, nicotine self-administration on a progressive-ratio schedule was not altered by intra-PPTg microinfusions of GABA agonists.
These data confirm that the PPTg is involved in nicotine self-administration, a conclusion that is independent of the schedule of reinforcement that is used. GABAergic mechanisms in the PPTg play a selective role in nicotine reinforcement compared to cocaine, and that role is restricted to the characteristics of reinforcement measured by fixed-ratio responding.</description><subject>Agonists</subject><subject>Animals</subject><subject>Baclofen</subject><subject>Biological and medical sciences</subject><subject>Brain Stem - drug effects</subject><subject>Brain Stem - physiology</subject><subject>Cocaine</subject><subject>Cocaine - administration & dosage</subject><subject>Dopamine Uptake Inhibitors - administration & dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug self-administration</subject><subject>GABA Agonists - pharmacology</subject><subject>Glutamatergic transmission</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mesencephalon</subject><subject>Muscimol</subject><subject>Neurons</subject><subject>Nicotine</subject><subject>Nicotine - administration & dosage</subject><subject>Nicotinic Agonists - administration & dosage</subject><subject>pedunculopontine nucleus</subject><subject>Pedunculopontine tegmental nucleus</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Reinforcement Schedule</subject><subject>Reinforcement schedules</subject><subject>Self Administration</subject><subject>Tegmentum Mesencephali - drug effects</subject><subject>Tegmentum Mesencephali - physiology</subject><subject>Tobacco, tobacco smoking</subject><subject>Toxicology</subject><subject>γ-Aminobutyric acid</subject><issn>0033-3158</issn><issn>1432-2072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</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>eNqF0U9vFCEUAHBibOxaPXo1kxi9TfuAYYHj2mg1aeKlnicM-7A0DDPyx6Qfwu8sa9c0epELBH68B-8R8orCOQWQFxmAUQ5trbb6CdnQgbOegWRPyQaA855ToU7J85zvoI1BDc_IKaUSGGi-IT-vdu933Yz21kSf59z52JVb7Fbc12hrWNYlFh-xK_htxlhM6GK1AetBulAx2oZNKr5hkzqTV7Qld4vrorfL76sZg-vNfvYtQ0mm-CUe9przPzDc_0nZTl6QE2dCxpfH-Yx8_fjh5vJTf_3l6vPl7rq3XKrST9pYmMDqLRNbcJRq7dSgmHTbyTmhAIXdOzFYIYVjOKDRigE3QphpQo38jLx7iLum5XvFXMbZZ4shmIhLzaNkTA68Feh_kCrGW0lVg2_-gXdLTbF9YuSt2lK3F8im-gdl05JzQjeuyc8m3Y8UxkM7x7_a2fzrY9Q6zbh_1Mf-NfD2CEy2JrhkovX50Q0gBRea_wK34Kmo</recordid><startdate>20011101</startdate><enddate>20011101</enddate><creator>CORRIGALL, William A</creator><creator>COEN, Kathleen M</creator><creator>JIANHUA ZHANG</creator><creator>ADAMSON, K. Laurel</creator><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>7X8</scope></search><sort><creationdate>20011101</creationdate><title>GABA mechanisms in the pedunculopontine tegmental nucleus influence particular aspects of nicotine self-administration selectively in the rat</title><author>CORRIGALL, William A ; COEN, Kathleen M ; JIANHUA ZHANG ; ADAMSON, K. Laurel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c378t-b9ac0b0c962560f1199f84827f6bff580e5cdf54c575f2e4ea98203a55abbe9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Agonists</topic><topic>Animals</topic><topic>Baclofen</topic><topic>Biological and medical sciences</topic><topic>Brain Stem - drug effects</topic><topic>Brain Stem - physiology</topic><topic>Cocaine</topic><topic>Cocaine - administration & dosage</topic><topic>Dopamine Uptake Inhibitors - administration & dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug self-administration</topic><topic>GABA Agonists - pharmacology</topic><topic>Glutamatergic transmission</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mesencephalon</topic><topic>Muscimol</topic><topic>Neurons</topic><topic>Nicotine</topic><topic>Nicotine - administration & dosage</topic><topic>Nicotinic Agonists - administration & dosage</topic><topic>pedunculopontine nucleus</topic><topic>Pedunculopontine tegmental nucleus</topic><topic>Rats</topic><topic>Rats, Long-Evans</topic><topic>Reinforcement Schedule</topic><topic>Reinforcement schedules</topic><topic>Self Administration</topic><topic>Tegmentum Mesencephali - drug effects</topic><topic>Tegmentum Mesencephali - physiology</topic><topic>Tobacco, tobacco smoking</topic><topic>Toxicology</topic><topic>γ-Aminobutyric acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CORRIGALL, William A</creatorcontrib><creatorcontrib>COEN, Kathleen M</creatorcontrib><creatorcontrib>JIANHUA ZHANG</creatorcontrib><creatorcontrib>ADAMSON, K. Laurel</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>Nursing & Allied Health Database</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>Psychology Database</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>MEDLINE - Academic</collection><jtitle>Psychopharmacologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CORRIGALL, William A</au><au>COEN, Kathleen M</au><au>JIANHUA ZHANG</au><au>ADAMSON, K. Laurel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GABA mechanisms in the pedunculopontine tegmental nucleus influence particular aspects of nicotine self-administration selectively in the rat</atitle><jtitle>Psychopharmacologia</jtitle><addtitle>Psychopharmacology (Berl)</addtitle><date>2001-11-01</date><risdate>2001</risdate><volume>158</volume><issue>2</issue><spage>190</spage><epage>197</epage><pages>190-197</pages><issn>0033-3158</issn><eissn>1432-2072</eissn><coden>PSYPAG</coden><abstract>The pedunculopontine tegmental nucleus (PPTg) is part of the neuronal circuit activated by self-administered nicotine. The cholinergic neurons of the PPTg comprise a prominent projection to midbrain dopamine neurons. However, anatomical studies of Fos expression suggest that nicotine targets primarily non-cholinergic neurons in the PPTg, especially GABAergic and glutamatergic neurons.
The objective of these experiments was to examine the role of GABA manipulations in the PPTg on nicotine self-administration.
Rats trained to self-administer nicotine or cocaine intravenously were prepared with brain microcannulae directed to the PPTg. Intra-PPTg microinfusions of the GABA agonists muscimol (10-50 ng) and baclofen (30-60 ng) reduced nicotine self-administration maintained on a fixed-ratio schedule of reinforcement (30 microg/kg per infusion); self-administration of cocaine (0.3 mg/kg per infusion) under an identical schedule was not affected. Muscimol and baclofen were also examined after intra-PPTg microinfusion in animals trained to self-administer nicotine on a progressive-ratio schedule (10 and 30 microg/kg per infusion). Progressive-ratio responding was sensitive to pharmacological manipulations such as a change in the nicotine dose available for self-administration, or intra-PPTg microinfusion of the nicotinic antagonist dihydro-beta-erythroidine (30 microg). However, nicotine self-administration on a progressive-ratio schedule was not altered by intra-PPTg microinfusions of GABA agonists.
These data confirm that the PPTg is involved in nicotine self-administration, a conclusion that is independent of the schedule of reinforcement that is used. GABAergic mechanisms in the PPTg play a selective role in nicotine reinforcement compared to cocaine, and that role is restricted to the characteristics of reinforcement measured by fixed-ratio responding.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>11702093</pmid><doi>10.1007/s002130100869</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0033-3158 |
ispartof | Psychopharmacologia, 2001-11, Vol.158 (2), p.190-197 |
issn | 0033-3158 1432-2072 |
language | eng |
recordid | cdi_proquest_miscellaneous_72274309 |
source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Agonists Animals Baclofen Biological and medical sciences Brain Stem - drug effects Brain Stem - physiology Cocaine Cocaine - administration & dosage Dopamine Uptake Inhibitors - administration & dosage Dose-Response Relationship, Drug Drug self-administration GABA Agonists - pharmacology Glutamatergic transmission Male Medical sciences Mesencephalon Muscimol Neurons Nicotine Nicotine - administration & dosage Nicotinic Agonists - administration & dosage pedunculopontine nucleus Pedunculopontine tegmental nucleus Rats Rats, Long-Evans Reinforcement Schedule Reinforcement schedules Self Administration Tegmentum Mesencephali - drug effects Tegmentum Mesencephali - physiology Tobacco, tobacco smoking Toxicology γ-Aminobutyric acid |
title | GABA mechanisms in the pedunculopontine tegmental nucleus influence particular aspects of nicotine self-administration selectively in the rat |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T15%3A54%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=GABA%20mechanisms%20in%20the%20pedunculopontine%20tegmental%20nucleus%20influence%20particular%20aspects%20of%20nicotine%20self-administration%20selectively%20in%20the%20rat&rft.jtitle=Psychopharmacologia&rft.au=CORRIGALL,%20William%20A&rft.date=2001-11-01&rft.volume=158&rft.issue=2&rft.spage=190&rft.epage=197&rft.pages=190-197&rft.issn=0033-3158&rft.eissn=1432-2072&rft.coden=PSYPAG&rft_id=info:doi/10.1007/s002130100869&rft_dat=%3Cproquest_cross%3E18234848%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3117799827&rft_id=info:pmid/11702093&rfr_iscdi=true |