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Serotonergic component of neuroleptic receptors
BINDING studies performed in vitro with 3 H-haloperidol 1–3 , 3 H-spiperone 4–5 , 3 H-dopamine 1–3,6 and 3 H-apomorphine 7,8 showed that the specific neuroleptic binding sites in the striatum are dopaminergic. The frontal cortex, however, was much more labelled by 3 H-spiperone than by 3 H-haloperid...
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Published in: | Nature (London) 1978-03, Vol.272 (5649), p.168-171 |
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container_end_page | 171 |
container_issue | 5649 |
container_start_page | 168 |
container_title | Nature (London) |
container_volume | 272 |
creator | LEYSEN, JOSÉE E NIEMEGEERS, CARLOS J. E TOLLENAERE, JAN P LADURON, PIERRE M |
description | BINDING studies performed
in vitro
with
3
H-haloperidol
1–3
,
3
H-spiperone
4–5
,
3
H-dopamine
1–3,6
and
3
H-apomorphine
7,8
showed that the specific neuroleptic binding sites in the striatum are dopaminergic. The frontal cortex, however, was much more labelled by
3
H-spiperone than by
3
H-haloperidol
9,10
. The investigations reported here indicate that the neuroleptic receptor sites in the frontal cortex labelled by
3
H-spiperone are predominantly serotonergic and virtually identical to those labelled by
3
H-LSD. These conclusions were reached from a study of the relative binding affinities of a series of serotonin or dopamine agonists or antagonists for rat frontal cortex and striatal receptors. Significant correlations were obtained between the binding activities in the rat frontal cortex and
in vivo
potencies in the pharmacological anti-tryptamine test. Similarly, binding activities in the striatum were significantly correlated with the potencies in the anti-apomorphine test. We therefore suggest that serotonergic, as well as dopaminergic, receptors are involved in the mechanism of action of neuroleptic drugs. |
doi_str_mv | 10.1038/272168a0 |
format | article |
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in vitro
with
3
H-haloperidol
1–3
,
3
H-spiperone
4–5
,
3
H-dopamine
1–3,6
and
3
H-apomorphine
7,8
showed that the specific neuroleptic binding sites in the striatum are dopaminergic. The frontal cortex, however, was much more labelled by
3
H-spiperone than by
3
H-haloperidol
9,10
. The investigations reported here indicate that the neuroleptic receptor sites in the frontal cortex labelled by
3
H-spiperone are predominantly serotonergic and virtually identical to those labelled by
3
H-LSD. These conclusions were reached from a study of the relative binding affinities of a series of serotonin or dopamine agonists or antagonists for rat frontal cortex and striatal receptors. Significant correlations were obtained between the binding activities in the rat frontal cortex and
in vivo
potencies in the pharmacological anti-tryptamine test. Similarly, binding activities in the striatum were significantly correlated with the potencies in the anti-apomorphine test. We therefore suggest that serotonergic, as well as dopaminergic, receptors are involved in the mechanism of action of neuroleptic drugs.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/272168a0</identifier><identifier>PMID: 564466</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Animals ; Apomorphine - antagonists & inhibitors ; Binding, Competitive ; Corpus Striatum - metabolism ; Frontal Lobe - metabolism ; Haloperidol - metabolism ; Humanities and Social Sciences ; Humans ; In Vitro Techniques ; letter ; Lysergic Acid Diethylamide - metabolism ; multidisciplinary ; Rats ; Receptors, Dopamine - metabolism ; Receptors, Serotonin - metabolism ; Science ; Science (multidisciplinary) ; Seizures - chemically induced ; Spiperone - metabolism ; Stereotyped Behavior - drug effects ; Tranquilizing Agents - metabolism ; Tranquilizing Agents - pharmacology ; Tryptamines</subject><ispartof>Nature (London), 1978-03, Vol.272 (5649), p.168-171</ispartof><rights>Springer Nature Limited 1978</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c429t-634b054d94a0c90184651c4ccb064715c15605284bed5ec5588efd7940c6a5693</citedby><cites>FETCH-LOGICAL-c429t-634b054d94a0c90184651c4ccb064715c15605284bed5ec5588efd7940c6a5693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2725,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/564466$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>LEYSEN, JOSÉE E</creatorcontrib><creatorcontrib>NIEMEGEERS, CARLOS J. E</creatorcontrib><creatorcontrib>TOLLENAERE, JAN P</creatorcontrib><creatorcontrib>LADURON, PIERRE M</creatorcontrib><title>Serotonergic component of neuroleptic receptors</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>BINDING studies performed
in vitro
with
3
H-haloperidol
1–3
,
3
H-spiperone
4–5
,
3
H-dopamine
1–3,6
and
3
H-apomorphine
7,8
showed that the specific neuroleptic binding sites in the striatum are dopaminergic. The frontal cortex, however, was much more labelled by
3
H-spiperone than by
3
H-haloperidol
9,10
. The investigations reported here indicate that the neuroleptic receptor sites in the frontal cortex labelled by
3
H-spiperone are predominantly serotonergic and virtually identical to those labelled by
3
H-LSD. These conclusions were reached from a study of the relative binding affinities of a series of serotonin or dopamine agonists or antagonists for rat frontal cortex and striatal receptors. Significant correlations were obtained between the binding activities in the rat frontal cortex and
in vivo
potencies in the pharmacological anti-tryptamine test. Similarly, binding activities in the striatum were significantly correlated with the potencies in the anti-apomorphine test. We therefore suggest that serotonergic, as well as dopaminergic, receptors are involved in the mechanism of action of neuroleptic drugs.</description><subject>Animals</subject><subject>Apomorphine - antagonists & inhibitors</subject><subject>Binding, Competitive</subject><subject>Corpus Striatum - metabolism</subject><subject>Frontal Lobe - metabolism</subject><subject>Haloperidol - metabolism</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>letter</subject><subject>Lysergic Acid Diethylamide - metabolism</subject><subject>multidisciplinary</subject><subject>Rats</subject><subject>Receptors, Dopamine - metabolism</subject><subject>Receptors, Serotonin - metabolism</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Seizures - chemically induced</subject><subject>Spiperone - metabolism</subject><subject>Stereotyped Behavior - drug effects</subject><subject>Tranquilizing Agents - metabolism</subject><subject>Tranquilizing Agents - pharmacology</subject><subject>Tryptamines</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1978</creationdate><recordtype>article</recordtype><recordid>eNptj01Lw0AQhhfxK1bBHyDSox5iZ5PZyeZYil9Q8KCeQ7KZlJY2G3aTg__elWhOnuaF5-FlXiGuJTxISPUiyRJJuoQjEUnMKEbS2bGIABIdg07pXFx4vwMAJTM8E6eKEIkisXhnZ3vbsttszdzYQxdy289tM295cHbPXR-AYxOCdf5SnDTl3vPV752Jz6fHj9VLvH57fl0t17HBJO9jSrEChXWOJZgcpEZS0qAxFRBmUhmpCFSiseJasVFKa27qLEcwVCrK05m4G3uNs947borObQ-l-yokFD-Li7_FQb0Z1W6oDlxP4jgx4PsR-wDaDbtiZwfXhuf_q7od3bbsB8dT1SR8A_vTZm4</recordid><startdate>19780309</startdate><enddate>19780309</enddate><creator>LEYSEN, JOSÉE E</creator><creator>NIEMEGEERS, CARLOS J. E</creator><creator>TOLLENAERE, JAN P</creator><creator>LADURON, PIERRE M</creator><general>Nature Publishing Group UK</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19780309</creationdate><title>Serotonergic component of neuroleptic receptors</title><author>LEYSEN, JOSÉE E ; NIEMEGEERS, CARLOS J. E ; TOLLENAERE, JAN P ; LADURON, PIERRE M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c429t-634b054d94a0c90184651c4ccb064715c15605284bed5ec5588efd7940c6a5693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1978</creationdate><topic>Animals</topic><topic>Apomorphine - antagonists & inhibitors</topic><topic>Binding, Competitive</topic><topic>Corpus Striatum - metabolism</topic><topic>Frontal Lobe - metabolism</topic><topic>Haloperidol - metabolism</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>letter</topic><topic>Lysergic Acid Diethylamide - metabolism</topic><topic>multidisciplinary</topic><topic>Rats</topic><topic>Receptors, Dopamine - metabolism</topic><topic>Receptors, Serotonin - metabolism</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Seizures - chemically induced</topic><topic>Spiperone - metabolism</topic><topic>Stereotyped Behavior - drug effects</topic><topic>Tranquilizing Agents - metabolism</topic><topic>Tranquilizing Agents - pharmacology</topic><topic>Tryptamines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LEYSEN, JOSÉE E</creatorcontrib><creatorcontrib>NIEMEGEERS, CARLOS J. E</creatorcontrib><creatorcontrib>TOLLENAERE, JAN P</creatorcontrib><creatorcontrib>LADURON, PIERRE M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LEYSEN, JOSÉE E</au><au>NIEMEGEERS, CARLOS J. E</au><au>TOLLENAERE, JAN P</au><au>LADURON, PIERRE M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serotonergic component of neuroleptic receptors</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>1978-03-09</date><risdate>1978</risdate><volume>272</volume><issue>5649</issue><spage>168</spage><epage>171</epage><pages>168-171</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><abstract>BINDING studies performed
in vitro
with
3
H-haloperidol
1–3
,
3
H-spiperone
4–5
,
3
H-dopamine
1–3,6
and
3
H-apomorphine
7,8
showed that the specific neuroleptic binding sites in the striatum are dopaminergic. The frontal cortex, however, was much more labelled by
3
H-spiperone than by
3
H-haloperidol
9,10
. The investigations reported here indicate that the neuroleptic receptor sites in the frontal cortex labelled by
3
H-spiperone are predominantly serotonergic and virtually identical to those labelled by
3
H-LSD. These conclusions were reached from a study of the relative binding affinities of a series of serotonin or dopamine agonists or antagonists for rat frontal cortex and striatal receptors. Significant correlations were obtained between the binding activities in the rat frontal cortex and
in vivo
potencies in the pharmacological anti-tryptamine test. Similarly, binding activities in the striatum were significantly correlated with the potencies in the anti-apomorphine test. We therefore suggest that serotonergic, as well as dopaminergic, receptors are involved in the mechanism of action of neuroleptic drugs.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>564466</pmid><doi>10.1038/272168a0</doi><tpages>4</tpages></addata></record> |
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language | eng |
recordid | cdi_crossref_primary_10_1038_272168a0 |
source | Nature |
subjects | Animals Apomorphine - antagonists & inhibitors Binding, Competitive Corpus Striatum - metabolism Frontal Lobe - metabolism Haloperidol - metabolism Humanities and Social Sciences Humans In Vitro Techniques letter Lysergic Acid Diethylamide - metabolism multidisciplinary Rats Receptors, Dopamine - metabolism Receptors, Serotonin - metabolism Science Science (multidisciplinary) Seizures - chemically induced Spiperone - metabolism Stereotyped Behavior - drug effects Tranquilizing Agents - metabolism Tranquilizing Agents - pharmacology Tryptamines |
title | Serotonergic component of neuroleptic receptors |
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