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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Veröffentlicht in:The international journal of neuropsychopharmacology 2017-11, Vol.20 (11), p.928-935
Hauptverfasser: 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
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container_end_page 935
container_issue 11
container_start_page 928
container_title The international journal of neuropsychopharmacology
container_volume 20
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.
doi_str_mv 10.1093/ijnp/pyx063
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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 &amp; 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. 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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><subject>Adult</subject><subject>Antipsychotic Agents - therapeutic use</subject><subject>Apomorphine - analogs &amp; 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 ; 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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.</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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source Oxford Journals Open Access Collection; MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
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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