Affinity States of Striatal Dopamine D2 Receptors in Antipsychotic-Free Patients with Schizophrenia
BackgroundDopamine D2 receptors are reported to have high-affinity (D2High) and low-affinity (D2Low) states. Although an increased proportion of D2High has been demonstrated in animal models of schizophrenia, few clinical studies have investigated this alteration of D2High in schizophrenia in vivo.M...
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creator | Kubota, Manabu Nagashima, Tomohisa Takano, Harumasa Kodaka, Fumitoshi Fujiwara, Hironobu Takahata, Keisuke Moriguchi, Sho Kimura, Yasuyuki Higuchi, Makoto Okubo, Yoshiro Takahashi, Hidehiko Ito, Hiroshi Suhara, Tetsuya |
description | BackgroundDopamine D2 receptors are reported to have high-affinity (D2High) and low-affinity (D2Low) states. Although an increased proportion of D2High has been demonstrated in animal models of schizophrenia, few clinical studies have investigated this alteration of D2High in schizophrenia in vivo.MethodsEleven patients with schizophrenia, including 10 antipsychotic-naive and 1 antipsychotic-free individuals, and 17 healthy controls were investigated. Psychopathology was assessed by Positive and Negative Syndrome Scale, and a 5-factor model was used. Two radioligands, [11C]raclopride and [11C]MNPA, were employed to quantify total dopamine D2 receptor and D2High, respectively, in the striatum by measuring their binding potentials. Binding potential values of [11C]raclopride and [11C]MNPA and the binding potential ratio of [11C]MNPA to [11C]raclopride in the striatal subregions were statistically compared between the 2 diagnostic groups using multivariate analysis of covariance controlling for age, gender, and smoking. Correlations between binding potential and Positive and Negative Syndrome Scale scores were also examined.ResultsMultivariate analysis of covariance demonstrated a significant effect of diagnosis (schizophrenia and control) on the binding potential ratio (P=.018), although the effects of diagnosis on binding potential values obtained with either [11C]raclopride or [11C]MNPA were nonsignificant. Posthoc test showed that the binding potential ratio was significantly higher in the putamen of patients (P=.017). The Positive and Negative Syndrome Scale “depressed” factor in patients was positively correlated with binding potential values of both ligands in the caudate.ConclusionsThe present study indicates the possibilities of: (1) a higher proportion of D2High in the putamen despite unaltered amounts of total dopamine D2 receptors; and (2) associations between depressive symptoms and amounts of caudate dopamine D2 receptors in patients with schizophrenia. |
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Although an increased proportion of D2High has been demonstrated in animal models of schizophrenia, few clinical studies have investigated this alteration of D2High in schizophrenia in vivo.MethodsEleven patients with schizophrenia, including 10 antipsychotic-naive and 1 antipsychotic-free individuals, and 17 healthy controls were investigated. Psychopathology was assessed by Positive and Negative Syndrome Scale, and a 5-factor model was used. Two radioligands, [11C]raclopride and [11C]MNPA, were employed to quantify total dopamine D2 receptor and D2High, respectively, in the striatum by measuring their binding potentials. Binding potential values of [11C]raclopride and [11C]MNPA and the binding potential ratio of [11C]MNPA to [11C]raclopride in the striatal subregions were statistically compared between the 2 diagnostic groups using multivariate analysis of covariance controlling for age, gender, and smoking. Correlations between binding potential and Positive and Negative Syndrome Scale scores were also examined.ResultsMultivariate analysis of covariance demonstrated a significant effect of diagnosis (schizophrenia and control) on the binding potential ratio (P=.018), although the effects of diagnosis on binding potential values obtained with either [11C]raclopride or [11C]MNPA were nonsignificant. Posthoc test showed that the binding potential ratio was significantly higher in the putamen of patients (P=.017). The Positive and Negative Syndrome Scale “depressed” factor in patients was positively correlated with binding potential values of both ligands in the caudate.ConclusionsThe present study indicates the possibilities of: (1) a higher proportion of D2High in the putamen despite unaltered amounts of total dopamine D2 receptors; and (2) associations between depressive symptoms and amounts of caudate dopamine D2 receptors in patients with schizophrenia.</description><identifier>ISSN: 1461-1457</identifier><identifier>EISSN: 1469-5111</identifier><identifier>DOI: 10.1093/ijnp/pyx063</identifier><identifier>PMID: 29016872</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Adult ; Antipsychotic Agents - therapeutic use ; Apomorphine - analogs & derivatives ; Apomorphine - pharmacokinetics ; Brain Mapping ; Corpus Striatum - diagnostic imaging ; Corpus Striatum - drug effects ; Corpus Striatum - metabolism ; Female ; Humans ; Male ; Positron-Emission Tomography ; Raclopride - pharmacokinetics ; Radioligand Assay ; Radiopharmaceuticals - pharmacokinetics ; Receptors, Dopamine D2 - metabolism ; Regular s ; Schizophrenia - drug therapy ; Schizophrenia - metabolism ; Schizophrenia - pathology ; Statistics as Topic ; Young Adult</subject><ispartof>The international journal of neuropsychopharmacology, 2017-11, Vol.20 (11), p.928-935</ispartof><rights>The Author 2017. Published by Oxford University Press on behalf of CINP. 2017</rights><rights>The Author 2017. Published by Oxford University Press on behalf of CINP.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-4f92e73a66104e83e74db1abeb74f323dac13e24498c3c1724e4e46d304d54803</citedby><cites>FETCH-LOGICAL-c456t-4f92e73a66104e83e74db1abeb74f323dac13e24498c3c1724e4e46d304d54803</cites><orcidid>0000-0002-7927-9483</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737675/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737675/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1598,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29016872$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kubota, Manabu</creatorcontrib><creatorcontrib>Nagashima, Tomohisa</creatorcontrib><creatorcontrib>Takano, Harumasa</creatorcontrib><creatorcontrib>Kodaka, Fumitoshi</creatorcontrib><creatorcontrib>Fujiwara, Hironobu</creatorcontrib><creatorcontrib>Takahata, Keisuke</creatorcontrib><creatorcontrib>Moriguchi, Sho</creatorcontrib><creatorcontrib>Kimura, Yasuyuki</creatorcontrib><creatorcontrib>Higuchi, Makoto</creatorcontrib><creatorcontrib>Okubo, Yoshiro</creatorcontrib><creatorcontrib>Takahashi, Hidehiko</creatorcontrib><creatorcontrib>Ito, Hiroshi</creatorcontrib><creatorcontrib>Suhara, Tetsuya</creatorcontrib><title>Affinity States of Striatal Dopamine D2 Receptors in Antipsychotic-Free Patients with Schizophrenia</title><title>The international journal of neuropsychopharmacology</title><addtitle>Int J Neuropsychopharmacol</addtitle><description>BackgroundDopamine D2 receptors are reported to have high-affinity (D2High) and low-affinity (D2Low) states. Although an increased proportion of D2High has been demonstrated in animal models of schizophrenia, few clinical studies have investigated this alteration of D2High in schizophrenia in vivo.MethodsEleven patients with schizophrenia, including 10 antipsychotic-naive and 1 antipsychotic-free individuals, and 17 healthy controls were investigated. Psychopathology was assessed by Positive and Negative Syndrome Scale, and a 5-factor model was used. Two radioligands, [11C]raclopride and [11C]MNPA, were employed to quantify total dopamine D2 receptor and D2High, respectively, in the striatum by measuring their binding potentials. Binding potential values of [11C]raclopride and [11C]MNPA and the binding potential ratio of [11C]MNPA to [11C]raclopride in the striatal subregions were statistically compared between the 2 diagnostic groups using multivariate analysis of covariance controlling for age, gender, and smoking. Correlations between binding potential and Positive and Negative Syndrome Scale scores were also examined.ResultsMultivariate analysis of covariance demonstrated a significant effect of diagnosis (schizophrenia and control) on the binding potential ratio (P=.018), although the effects of diagnosis on binding potential values obtained with either [11C]raclopride or [11C]MNPA were nonsignificant. Posthoc test showed that the binding potential ratio was significantly higher in the putamen of patients (P=.017). The Positive and Negative Syndrome Scale “depressed” factor in patients was positively correlated with binding potential values of both ligands in the caudate.ConclusionsThe present study indicates the possibilities of: (1) a higher proportion of D2High in the putamen despite unaltered amounts of total dopamine D2 receptors; and (2) associations between depressive symptoms and amounts of caudate dopamine D2 receptors in patients with schizophrenia.</description><subject>Adult</subject><subject>Antipsychotic Agents - therapeutic use</subject><subject>Apomorphine - analogs & derivatives</subject><subject>Apomorphine - pharmacokinetics</subject><subject>Brain Mapping</subject><subject>Corpus Striatum - diagnostic imaging</subject><subject>Corpus Striatum - drug effects</subject><subject>Corpus Striatum - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Positron-Emission Tomography</subject><subject>Raclopride - pharmacokinetics</subject><subject>Radioligand Assay</subject><subject>Radiopharmaceuticals - pharmacokinetics</subject><subject>Receptors, Dopamine D2 - metabolism</subject><subject>Regular s</subject><subject>Schizophrenia - drug therapy</subject><subject>Schizophrenia - metabolism</subject><subject>Schizophrenia - pathology</subject><subject>Statistics as Topic</subject><subject>Young Adult</subject><issn>1461-1457</issn><issn>1469-5111</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNp9kctrGzEQxkVJaB7tqfegUwiETfRayXspmLwh0FK3ZyFrZ7sKa0mR5DbOX59N7YT0EuYwA_Pjm4_5EPpCyQklDT91dz6extUDkfwD2qVCNlVNKd36N9OKilrtoL2c7whhoubyI9phDaFyotgustOuc96VFZ4VUyDj0I1TcqaYAZ-HaBbOAz5n-AdYiCWkjJ3HU19czCvbh-JsdZkA8HdTHPiS8V9XejyzvXsMsU_gnfmEtjszZPi86fvo1-XFz7Pr6vbb1c3Z9LayopalEl3DQHEjJSUCJhyUaOfUzGGuRMcZb42lHJgQzcRySxUTMJZsORFtLSaE76Ova924nC-gtaOdZAYdk1uYtNLBOP3_xrte_w5_dK24kqoeBY42AincLyEXvXDZwjAYD2GZNW3q8W-8YWxEj9eoTSHnBN3rGUr0cyz6ORa9jmWkD946e2VfchiBwzUQlvFdpSfSe5kh</recordid><startdate>20171101</startdate><enddate>20171101</enddate><creator>Kubota, Manabu</creator><creator>Nagashima, Tomohisa</creator><creator>Takano, Harumasa</creator><creator>Kodaka, Fumitoshi</creator><creator>Fujiwara, Hironobu</creator><creator>Takahata, Keisuke</creator><creator>Moriguchi, Sho</creator><creator>Kimura, Yasuyuki</creator><creator>Higuchi, Makoto</creator><creator>Okubo, Yoshiro</creator><creator>Takahashi, Hidehiko</creator><creator>Ito, Hiroshi</creator><creator>Suhara, Tetsuya</creator><general>Oxford University Press</general><scope>TOX</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7927-9483</orcidid></search><sort><creationdate>20171101</creationdate><title>Affinity States of Striatal Dopamine D2 Receptors in Antipsychotic-Free Patients with Schizophrenia</title><author>Kubota, Manabu ; Nagashima, Tomohisa ; Takano, Harumasa ; Kodaka, Fumitoshi ; Fujiwara, Hironobu ; Takahata, Keisuke ; Moriguchi, Sho ; Kimura, Yasuyuki ; Higuchi, Makoto ; Okubo, Yoshiro ; Takahashi, Hidehiko ; Ito, Hiroshi ; Suhara, Tetsuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-4f92e73a66104e83e74db1abeb74f323dac13e24498c3c1724e4e46d304d54803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Antipsychotic Agents - therapeutic use</topic><topic>Apomorphine - analogs & derivatives</topic><topic>Apomorphine - pharmacokinetics</topic><topic>Brain Mapping</topic><topic>Corpus Striatum - diagnostic imaging</topic><topic>Corpus Striatum - drug effects</topic><topic>Corpus Striatum - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Positron-Emission Tomography</topic><topic>Raclopride - pharmacokinetics</topic><topic>Radioligand Assay</topic><topic>Radiopharmaceuticals - pharmacokinetics</topic><topic>Receptors, Dopamine D2 - metabolism</topic><topic>Regular s</topic><topic>Schizophrenia - drug therapy</topic><topic>Schizophrenia - metabolism</topic><topic>Schizophrenia - pathology</topic><topic>Statistics as Topic</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kubota, Manabu</creatorcontrib><creatorcontrib>Nagashima, Tomohisa</creatorcontrib><creatorcontrib>Takano, Harumasa</creatorcontrib><creatorcontrib>Kodaka, Fumitoshi</creatorcontrib><creatorcontrib>Fujiwara, Hironobu</creatorcontrib><creatorcontrib>Takahata, Keisuke</creatorcontrib><creatorcontrib>Moriguchi, Sho</creatorcontrib><creatorcontrib>Kimura, Yasuyuki</creatorcontrib><creatorcontrib>Higuchi, Makoto</creatorcontrib><creatorcontrib>Okubo, Yoshiro</creatorcontrib><creatorcontrib>Takahashi, Hidehiko</creatorcontrib><creatorcontrib>Ito, Hiroshi</creatorcontrib><creatorcontrib>Suhara, Tetsuya</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The international journal of neuropsychopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kubota, Manabu</au><au>Nagashima, Tomohisa</au><au>Takano, Harumasa</au><au>Kodaka, Fumitoshi</au><au>Fujiwara, Hironobu</au><au>Takahata, Keisuke</au><au>Moriguchi, Sho</au><au>Kimura, Yasuyuki</au><au>Higuchi, Makoto</au><au>Okubo, Yoshiro</au><au>Takahashi, Hidehiko</au><au>Ito, Hiroshi</au><au>Suhara, Tetsuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Affinity States of Striatal Dopamine D2 Receptors in Antipsychotic-Free Patients with Schizophrenia</atitle><jtitle>The international journal of neuropsychopharmacology</jtitle><addtitle>Int J Neuropsychopharmacol</addtitle><date>2017-11-01</date><risdate>2017</risdate><volume>20</volume><issue>11</issue><spage>928</spage><epage>935</epage><pages>928-935</pages><issn>1461-1457</issn><eissn>1469-5111</eissn><abstract>BackgroundDopamine D2 receptors are reported to have high-affinity (D2High) and low-affinity (D2Low) states. Although an increased proportion of D2High has been demonstrated in animal models of schizophrenia, few clinical studies have investigated this alteration of D2High in schizophrenia in vivo.MethodsEleven patients with schizophrenia, including 10 antipsychotic-naive and 1 antipsychotic-free individuals, and 17 healthy controls were investigated. Psychopathology was assessed by Positive and Negative Syndrome Scale, and a 5-factor model was used. Two radioligands, [11C]raclopride and [11C]MNPA, were employed to quantify total dopamine D2 receptor and D2High, respectively, in the striatum by measuring their binding potentials. Binding potential values of [11C]raclopride and [11C]MNPA and the binding potential ratio of [11C]MNPA to [11C]raclopride in the striatal subregions were statistically compared between the 2 diagnostic groups using multivariate analysis of covariance controlling for age, gender, and smoking. Correlations between binding potential and Positive and Negative Syndrome Scale scores were also examined.ResultsMultivariate analysis of covariance demonstrated a significant effect of diagnosis (schizophrenia and control) on the binding potential ratio (P=.018), although the effects of diagnosis on binding potential values obtained with either [11C]raclopride or [11C]MNPA were nonsignificant. Posthoc test showed that the binding potential ratio was significantly higher in the putamen of patients (P=.017). The Positive and Negative Syndrome Scale “depressed” factor in patients was positively correlated with binding potential values of both ligands in the caudate.ConclusionsThe present study indicates the possibilities of: (1) a higher proportion of D2High in the putamen despite unaltered amounts of total dopamine D2 receptors; and (2) associations between depressive symptoms and amounts of caudate dopamine D2 receptors in patients with schizophrenia.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>29016872</pmid><doi>10.1093/ijnp/pyx063</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-7927-9483</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Antipsychotic Agents - therapeutic use Apomorphine - analogs & derivatives Apomorphine - pharmacokinetics Brain Mapping Corpus Striatum - diagnostic imaging Corpus Striatum - drug effects Corpus Striatum - metabolism Female Humans Male Positron-Emission Tomography Raclopride - pharmacokinetics Radioligand Assay Radiopharmaceuticals - pharmacokinetics Receptors, Dopamine D2 - metabolism Regular s Schizophrenia - drug therapy Schizophrenia - metabolism Schizophrenia - pathology Statistics as Topic Young Adult |
title | Affinity States of Striatal Dopamine D2 Receptors in Antipsychotic-Free Patients with Schizophrenia |
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