Effects of dopaminergic modulation on automatic semantic priming: a double-blind study
Background Enhanced automatic spreading of activation in the semantic network has been suggested to underlie formal thought disorder in patients with schizophrenia, but it is not clear how this relates to the dopaminergic dysfunction implicated in the disorder. Previous studies on dopaminergic modul...
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description | Background Enhanced automatic spreading of activation in the semantic network has been suggested to underlie formal thought disorder in patients with schizophrenia, but it is not clear how this relates to the dopaminergic dysfunction implicated in the disorder. Previous studies on dopaminergic modulation of priming in healthy volunteers have focused on controlled rather than automatic processes. The present study aimed to examine the effects of both a dopaminergic agonist and a dopaminergic antagonist on semantic priming while minimizing the contribution of controlled processes. Methods We investigated the effects of levodopa (L-Dopa; 100 mg), haloperidol (2 mg) and placebo on priming in healthy participants within a randomized, double-blind, crossover design. We used a pronunciation priming task with word triplets; the middle word was an ambiguous word, whereas the first word of the triplet served to provide either a congruent, incongruent or unbiased context for the target word. Two stimulus onset asynchronies (SOA) were used: 150 ms and 750 ms. Results The study involved 34 participants. At an SOA of 150 ms, L-Dopa accelerated responses to incongruent targets and subordinate targets of ambiguous words, whereas haloperidol was associated with faster responses in congruent contexts and dominant targets. At an SOA of 750 ms, haloperidol accelerated responses to subordinate targets. Limitations Modulations in the relative magnitude of priming according to substance and condition rather than absolute priming were assessed. Conclusion Effects of L-Dopa on automatic priming processes appear to be different than those on controlled processes. Our results are consistent with those of studies on semantic priming and the effects on antipsychotics in patients with schizophrenia. |
doi_str_mv | 10.1503/jpn.130035 |
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Previous studies on dopaminergic modulation of priming in healthy volunteers have focused on controlled rather than automatic processes. The present study aimed to examine the effects of both a dopaminergic agonist and a dopaminergic antagonist on semantic priming while minimizing the contribution of controlled processes. Methods We investigated the effects of levodopa (L-Dopa; 100 mg), haloperidol (2 mg) and placebo on priming in healthy participants within a randomized, double-blind, crossover design. We used a pronunciation priming task with word triplets; the middle word was an ambiguous word, whereas the first word of the triplet served to provide either a congruent, incongruent or unbiased context for the target word. Two stimulus onset asynchronies (SOA) were used: 150 ms and 750 ms. Results The study involved 34 participants. At an SOA of 150 ms, L-Dopa accelerated responses to incongruent targets and subordinate targets of ambiguous words, whereas haloperidol was associated with faster responses in congruent contexts and dominant targets. At an SOA of 750 ms, haloperidol accelerated responses to subordinate targets. Limitations Modulations in the relative magnitude of priming according to substance and condition rather than absolute priming were assessed. Conclusion Effects of L-Dopa on automatic priming processes appear to be different than those on controlled processes. Our results are consistent with those of studies on semantic priming and the effects on antipsychotics in patients with schizophrenia.</description><identifier>ISSN: 1180-4882</identifier><identifier>EISSN: 1488-2434</identifier><identifier>DOI: 10.1503/jpn.130035</identifier><identifier>PMID: 24099637</identifier><identifier>CODEN: JPNEEF</identifier><language>eng</language><publisher>Ottawa, ON: Canadian Medical Association</publisher><subject>Adult ; Antipsychotic drugs ; Biological and medical sciences ; Cross-Over Studies ; Design ; Dopamine - metabolism ; Dopamine Agents - pharmacology ; Dopamine Antagonists - pharmacology ; Dopaminergic mechanisms ; Dosage and administration ; Double-Blind Method ; Drug therapy ; Experimental design ; Female ; Fundamental and applied biological sciences. Psychology ; Haloperidol - pharmacology ; Humans ; Levodopa - pharmacology ; Male ; Medical Education ; Medical imaging ; Medical sciences ; Methods ; Pattern Recognition, Visual - drug effects ; Pattern Recognition, Visual - physiology ; Physiological aspects ; Priming (Psychology) ; Psychiatry ; Psychoanalysis ; Psychology. Psychoanalysis. Psychiatry ; Psychology. Psychophysiology ; Psychopathology. Psychiatry ; Reaction Time - drug effects ; Reading ; Repetition Priming - drug effects ; Repetition Priming - physiology ; Research Papers ; Schizophrenia ; Semantics ; Speech - drug effects ; Speech - physiology ; Studies ; Young Adult</subject><ispartof>Journal of psychiatry & neuroscience, 2014-03, Vol.39 (2), p.110-117</ispartof><rights>Canadian Medical Association</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2014 Joule Inc.</rights><rights>Copyright Canadian Medical Association Mar 2014</rights><rights>2014 Canadian Medical Association 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c722t-84a171cb910e01bd25baba254adb227418aa0906dc64c0aeff392329d8de1e003</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937279/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937279/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28765355$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24099637$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Andreou, Christina, MD, PhD</creatorcontrib><creatorcontrib>Veith, Kristina, MD, PhD</creatorcontrib><creatorcontrib>Moritz, Steffen</creatorcontrib><creatorcontrib>Bozikas, Vasilis P., PhD</creatorcontrib><creatorcontrib>Lincoln, Tania M., PhD</creatorcontrib><title>Effects of dopaminergic modulation on automatic semantic priming: a double-blind study</title><title>Journal of psychiatry & neuroscience</title><addtitle>J Psychiatry Neurosci</addtitle><description>Background Enhanced automatic spreading of activation in the semantic network has been suggested to underlie formal thought disorder in patients with schizophrenia, but it is not clear how this relates to the dopaminergic dysfunction implicated in the disorder. Previous studies on dopaminergic modulation of priming in healthy volunteers have focused on controlled rather than automatic processes. The present study aimed to examine the effects of both a dopaminergic agonist and a dopaminergic antagonist on semantic priming while minimizing the contribution of controlled processes. Methods We investigated the effects of levodopa (L-Dopa; 100 mg), haloperidol (2 mg) and placebo on priming in healthy participants within a randomized, double-blind, crossover design. We used a pronunciation priming task with word triplets; the middle word was an ambiguous word, whereas the first word of the triplet served to provide either a congruent, incongruent or unbiased context for the target word. Two stimulus onset asynchronies (SOA) were used: 150 ms and 750 ms. Results The study involved 34 participants. At an SOA of 150 ms, L-Dopa accelerated responses to incongruent targets and subordinate targets of ambiguous words, whereas haloperidol was associated with faster responses in congruent contexts and dominant targets. At an SOA of 750 ms, haloperidol accelerated responses to subordinate targets. Limitations Modulations in the relative magnitude of priming according to substance and condition rather than absolute priming were assessed. Conclusion Effects of L-Dopa on automatic priming processes appear to be different than those on controlled processes. Our results are consistent with those of studies on semantic priming and the effects on antipsychotics in patients with schizophrenia.</description><subject>Adult</subject><subject>Antipsychotic drugs</subject><subject>Biological and medical sciences</subject><subject>Cross-Over Studies</subject><subject>Design</subject><subject>Dopamine - metabolism</subject><subject>Dopamine Agents - pharmacology</subject><subject>Dopamine Antagonists - pharmacology</subject><subject>Dopaminergic mechanisms</subject><subject>Dosage and administration</subject><subject>Double-Blind Method</subject><subject>Drug therapy</subject><subject>Experimental design</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Haloperidol - pharmacology</subject><subject>Humans</subject><subject>Levodopa - pharmacology</subject><subject>Male</subject><subject>Medical Education</subject><subject>Medical imaging</subject><subject>Medical sciences</subject><subject>Methods</subject><subject>Pattern Recognition, Visual - drug effects</subject><subject>Pattern Recognition, Visual - physiology</subject><subject>Physiological aspects</subject><subject>Priming (Psychology)</subject><subject>Psychiatry</subject><subject>Psychoanalysis</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychology. Psychophysiology</subject><subject>Psychopathology. Psychiatry</subject><subject>Reaction Time - drug effects</subject><subject>Reading</subject><subject>Repetition Priming - drug effects</subject><subject>Repetition Priming - physiology</subject><subject>Research Papers</subject><subject>Schizophrenia</subject><subject>Semantics</subject><subject>Speech - drug effects</subject><subject>Speech - physiology</subject><subject>Studies</subject><subject>Young Adult</subject><issn>1180-4882</issn><issn>1488-2434</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqVk11v0zAUhiMEYmNwww9AERMIkFL8kQ-HC6RpGjBpAokBt9aJc5K6OHYXJxP99zi0rC3qDYql2MlzXtvnvCeKnlIyoxnhbxdLO6OcEJ7di45pKkTCUp7eD3MqSBLW7Ch65P2CEMIIzR5GRywlZZnz4jj6cdE0qAYfuyau3RI6bbFvtYo7V48GBu1sHAaMg-vCSsUeO7DTZNnrALfvYgiBY2UwqYy2deyHsV49jh40YDw-2bxPou8fLr6df0quvny8PD-7SlTB2JCIFGhBVVVSgoRWNcsqqIBlKdQVY0VKBQApSV6rPFUEsGl4yTgra1EjxXDjk-j9Wnc5Vh3WCu3Qg5HT2aBfSQda7v-xei5bdyt5yQtWlEHg1Uagdzcj-kF22is0Biy60cspwVlaFoIH9PQfdOHG3obrTZQoBM1FsaVaMCi1bVzYV02i8oznvCShUpNWcoBqMSQfjLPY6PB5j39-gFdLfSN3odkBKDw1dlodVH29FxCYAX8NLYzey8vrr__Bft5nX-6wcwQzzL0z4-Qmvw--WYOqd9732NxVjpI_qZfB23Lt7QA_2631HfrXzAF4sQHAKzBND1Zpv-VEkWc8y7amweDMW429VMG5OoT8xBX6bVWlZ5LI66mNpi6iaTZ1EOG_AUp-EO0</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Andreou, Christina, MD, PhD</creator><creator>Veith, Kristina, MD, PhD</creator><creator>Moritz, Steffen</creator><creator>Bozikas, Vasilis P., PhD</creator><creator>Lincoln, Tania M., PhD</creator><general>Canadian Medical Association</general><general>Joule Inc</general><general>CMA Impact, Inc</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>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>8FV</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M3G</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140301</creationdate><title>Effects of dopaminergic modulation on automatic semantic priming: a double-blind study</title><author>Andreou, Christina, MD, PhD ; Veith, Kristina, MD, PhD ; Moritz, Steffen ; Bozikas, Vasilis P., PhD ; Lincoln, Tania M., PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c722t-84a171cb910e01bd25baba254adb227418aa0906dc64c0aeff392329d8de1e003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Antipsychotic drugs</topic><topic>Biological and medical sciences</topic><topic>Cross-Over Studies</topic><topic>Design</topic><topic>Dopamine - metabolism</topic><topic>Dopamine Agents - pharmacology</topic><topic>Dopamine Antagonists - pharmacology</topic><topic>Dopaminergic mechanisms</topic><topic>Dosage and administration</topic><topic>Double-Blind Method</topic><topic>Drug therapy</topic><topic>Experimental design</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Haloperidol - pharmacology</topic><topic>Humans</topic><topic>Levodopa - pharmacology</topic><topic>Male</topic><topic>Medical Education</topic><topic>Medical imaging</topic><topic>Medical sciences</topic><topic>Methods</topic><topic>Pattern Recognition, Visual - drug effects</topic><topic>Pattern Recognition, Visual - physiology</topic><topic>Physiological aspects</topic><topic>Priming (Psychology)</topic><topic>Psychiatry</topic><topic>Psychoanalysis</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychology. Psychophysiology</topic><topic>Psychopathology. Psychiatry</topic><topic>Reaction Time - drug effects</topic><topic>Reading</topic><topic>Repetition Priming - drug effects</topic><topic>Repetition Priming - physiology</topic><topic>Research Papers</topic><topic>Schizophrenia</topic><topic>Semantics</topic><topic>Speech - drug effects</topic><topic>Speech - physiology</topic><topic>Studies</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andreou, Christina, MD, PhD</creatorcontrib><creatorcontrib>Veith, Kristina, MD, PhD</creatorcontrib><creatorcontrib>Moritz, Steffen</creatorcontrib><creatorcontrib>Bozikas, Vasilis P., PhD</creatorcontrib><creatorcontrib>Lincoln, Tania M., PhD</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>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</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>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Canadian Business & Current Affairs Database</collection><collection>Canadian Business & Current Affairs Database (Alumni Edition)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>CBCA Reference & Current Events</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of psychiatry & neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andreou, Christina, MD, PhD</au><au>Veith, Kristina, MD, PhD</au><au>Moritz, Steffen</au><au>Bozikas, Vasilis P., PhD</au><au>Lincoln, Tania M., PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of dopaminergic modulation on automatic semantic priming: a double-blind study</atitle><jtitle>Journal of psychiatry & neuroscience</jtitle><addtitle>J Psychiatry Neurosci</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>39</volume><issue>2</issue><spage>110</spage><epage>117</epage><pages>110-117</pages><issn>1180-4882</issn><eissn>1488-2434</eissn><coden>JPNEEF</coden><abstract>Background Enhanced automatic spreading of activation in the semantic network has been suggested to underlie formal thought disorder in patients with schizophrenia, but it is not clear how this relates to the dopaminergic dysfunction implicated in the disorder. Previous studies on dopaminergic modulation of priming in healthy volunteers have focused on controlled rather than automatic processes. The present study aimed to examine the effects of both a dopaminergic agonist and a dopaminergic antagonist on semantic priming while minimizing the contribution of controlled processes. Methods We investigated the effects of levodopa (L-Dopa; 100 mg), haloperidol (2 mg) and placebo on priming in healthy participants within a randomized, double-blind, crossover design. We used a pronunciation priming task with word triplets; the middle word was an ambiguous word, whereas the first word of the triplet served to provide either a congruent, incongruent or unbiased context for the target word. Two stimulus onset asynchronies (SOA) were used: 150 ms and 750 ms. Results The study involved 34 participants. At an SOA of 150 ms, L-Dopa accelerated responses to incongruent targets and subordinate targets of ambiguous words, whereas haloperidol was associated with faster responses in congruent contexts and dominant targets. At an SOA of 750 ms, haloperidol accelerated responses to subordinate targets. Limitations Modulations in the relative magnitude of priming according to substance and condition rather than absolute priming were assessed. Conclusion Effects of L-Dopa on automatic priming processes appear to be different than those on controlled processes. Our results are consistent with those of studies on semantic priming and the effects on antipsychotics in patients with schizophrenia.</abstract><cop>Ottawa, ON</cop><pub>Canadian Medical Association</pub><pmid>24099637</pmid><doi>10.1503/jpn.130035</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Antipsychotic drugs Biological and medical sciences Cross-Over Studies Design Dopamine - metabolism Dopamine Agents - pharmacology Dopamine Antagonists - pharmacology Dopaminergic mechanisms Dosage and administration Double-Blind Method Drug therapy Experimental design Female Fundamental and applied biological sciences. Psychology Haloperidol - pharmacology Humans Levodopa - pharmacology Male Medical Education Medical imaging Medical sciences Methods Pattern Recognition, Visual - drug effects Pattern Recognition, Visual - physiology Physiological aspects Priming (Psychology) Psychiatry Psychoanalysis Psychology. Psychoanalysis. Psychiatry Psychology. Psychophysiology Psychopathology. Psychiatry Reaction Time - drug effects Reading Repetition Priming - drug effects Repetition Priming - physiology Research Papers Schizophrenia Semantics Speech - drug effects Speech - physiology Studies Young Adult |
title | Effects of dopaminergic modulation on automatic semantic priming: a double-blind study |
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