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Lateralization of the serotonin-1A receptor distribution in language areas revealed by PET
Lateralization is a well described aspect of the human brain. A plethora of morphological, cytological and functional studies describes hemispheric asymmetry in auditory and language areas. However, no study has reported cortical lateralization in the healthy human brain in vivo on the level of neur...
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Published in: | NeuroImage (Orlando, Fla.) Fla.), 2009-04, Vol.45 (2), p.598-605 |
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description | Lateralization is a well described aspect of the human brain. A plethora of morphological, cytological and functional studies describes hemispheric asymmetry in auditory and language areas. However, no study has reported cortical lateralization in the healthy human brain in vivo on the level of neurotransmitter receptors and in relation to functional organization so far. In this study, we assessed the distribution of the main inhibitory serotonergic receptor (the 5-HT1A receptor) and analyzed its regional binding with regard to hemisphere, sex and plasma levels of sex steroid hormones (testosterone, estradiol, progesterone). We quantified the 5-HT1A receptor binding potential by positron emission tomography (PET) using the highly selective and specific radioligand [carbonyl-11C]WAY-100635 and measured hormone levels in thirty-four (16 females, 18 males) healthy right-handed subjects. The obtained data were analyzed in an automated region of interest (ROI) based approach investigating 14 auditory, language and limbic areas. We found significantly higher 5-HT1A receptor binding in the superior and middle frontal gyri of the right hemisphere, the triangular and orbital parts of the inferior frontal gyrus, the supramarginal gyrus, the superior gyrus of the temporal pole and the middle temporal gyrus. Regions of the primary and secondary auditory cortex (Heschl's gyrus and superior temporal gyrus) and the Rolandic operculum displayed significantly higher receptor binding in the left hemisphere. 5-HT1A receptor binding was 1.8–2.9% higher in right frontal ROIs and 2–3.6% higher in left primary and secondary auditory regions. There was no hemispheric difference in 5-HT1A receptor binding in the hippocampus, amygdala, and insula. Post-hoc testing suggested that lateralization of 5-HT1A receptor binding differed between the sexes in the triangular part of the inferior frontal gyrus. For the first time, this PET study shows lateralization of the main inhibitory receptor of the serotonergic system in functionally asymmetric organized regions of the healthy human brain in vivo. |
doi_str_mv | 10.1016/j.neuroimage.2008.11.033 |
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A plethora of morphological, cytological and functional studies describes hemispheric asymmetry in auditory and language areas. However, no study has reported cortical lateralization in the healthy human brain in vivo on the level of neurotransmitter receptors and in relation to functional organization so far. In this study, we assessed the distribution of the main inhibitory serotonergic receptor (the 5-HT1A receptor) and analyzed its regional binding with regard to hemisphere, sex and plasma levels of sex steroid hormones (testosterone, estradiol, progesterone). We quantified the 5-HT1A receptor binding potential by positron emission tomography (PET) using the highly selective and specific radioligand [carbonyl-11C]WAY-100635 and measured hormone levels in thirty-four (16 females, 18 males) healthy right-handed subjects. The obtained data were analyzed in an automated region of interest (ROI) based approach investigating 14 auditory, language and limbic areas. We found significantly higher 5-HT1A receptor binding in the superior and middle frontal gyri of the right hemisphere, the triangular and orbital parts of the inferior frontal gyrus, the supramarginal gyrus, the superior gyrus of the temporal pole and the middle temporal gyrus. Regions of the primary and secondary auditory cortex (Heschl's gyrus and superior temporal gyrus) and the Rolandic operculum displayed significantly higher receptor binding in the left hemisphere. 5-HT1A receptor binding was 1.8–2.9% higher in right frontal ROIs and 2–3.6% higher in left primary and secondary auditory regions. There was no hemispheric difference in 5-HT1A receptor binding in the hippocampus, amygdala, and insula. Post-hoc testing suggested that lateralization of 5-HT1A receptor binding differed between the sexes in the triangular part of the inferior frontal gyrus. For the first time, this PET study shows lateralization of the main inhibitory receptor of the serotonergic system in functionally asymmetric organized regions of the healthy human brain in vivo.</description><identifier>ISSN: 1053-8119</identifier><identifier>EISSN: 1095-9572</identifier><identifier>DOI: 10.1016/j.neuroimage.2008.11.033</identifier><identifier>PMID: 19103294</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>5-HT1A ; Adult ; Asymmetry ; Auditory Perception - physiology ; Brain ; Brain - diagnostic imaging ; Brain - physiology ; Brain asymmetry ; Brain research ; Carbon Radioisotopes - pharmacokinetics ; Female ; Females ; Functional Laterality - physiology ; Gender differences ; Humans ; Language ; Lateralization ; Male ; Menstruation ; Piperazines - pharmacokinetics ; Plasma ; Positron-Emission Tomography - methods ; Pyridines - pharmacokinetics ; Receptor, Serotonin, 5-HT1A - metabolism ; Serotonin ; Serotonin Antagonists - pharmacokinetics ; Sex hormones ; Studies ; Testosterone ; Tissue Distribution</subject><ispartof>NeuroImage (Orlando, Fla.), 2009-04, Vol.45 (2), p.598-605</ispartof><rights>2009</rights><rights>Copyright Elsevier Limited Apr 1, 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-851ee7e39653fb00c7e63b66350e375cb4deeb250364059ac2cfd4475cd29c9c3</citedby><cites>FETCH-LOGICAL-c431t-851ee7e39653fb00c7e63b66350e375cb4deeb250364059ac2cfd4475cd29c9c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19103294$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fink, Martin</creatorcontrib><creatorcontrib>Wadsak, Wolfgang</creatorcontrib><creatorcontrib>Savli, Markus</creatorcontrib><creatorcontrib>Stein, Patrycja</creatorcontrib><creatorcontrib>Moser, Ulrike</creatorcontrib><creatorcontrib>Hahn, Andreas</creatorcontrib><creatorcontrib>Mien, Leonhard-Key</creatorcontrib><creatorcontrib>Kletter, Kurt</creatorcontrib><creatorcontrib>Mitterhauser, Markus</creatorcontrib><creatorcontrib>Kasper, Siegfried</creatorcontrib><creatorcontrib>Lanzenberger, Rupert</creatorcontrib><title>Lateralization of the serotonin-1A receptor distribution in language areas revealed by PET</title><title>NeuroImage (Orlando, Fla.)</title><addtitle>Neuroimage</addtitle><description>Lateralization is a well described aspect of the human brain. A plethora of morphological, cytological and functional studies describes hemispheric asymmetry in auditory and language areas. However, no study has reported cortical lateralization in the healthy human brain in vivo on the level of neurotransmitter receptors and in relation to functional organization so far. In this study, we assessed the distribution of the main inhibitory serotonergic receptor (the 5-HT1A receptor) and analyzed its regional binding with regard to hemisphere, sex and plasma levels of sex steroid hormones (testosterone, estradiol, progesterone). We quantified the 5-HT1A receptor binding potential by positron emission tomography (PET) using the highly selective and specific radioligand [carbonyl-11C]WAY-100635 and measured hormone levels in thirty-four (16 females, 18 males) healthy right-handed subjects. The obtained data were analyzed in an automated region of interest (ROI) based approach investigating 14 auditory, language and limbic areas. We found significantly higher 5-HT1A receptor binding in the superior and middle frontal gyri of the right hemisphere, the triangular and orbital parts of the inferior frontal gyrus, the supramarginal gyrus, the superior gyrus of the temporal pole and the middle temporal gyrus. Regions of the primary and secondary auditory cortex (Heschl's gyrus and superior temporal gyrus) and the Rolandic operculum displayed significantly higher receptor binding in the left hemisphere. 5-HT1A receptor binding was 1.8–2.9% higher in right frontal ROIs and 2–3.6% higher in left primary and secondary auditory regions. There was no hemispheric difference in 5-HT1A receptor binding in the hippocampus, amygdala, and insula. Post-hoc testing suggested that lateralization of 5-HT1A receptor binding differed between the sexes in the triangular part of the inferior frontal gyrus. For the first time, this PET study shows lateralization of the main inhibitory receptor of the serotonergic system in functionally asymmetric organized regions of the healthy human brain in vivo.</description><subject>5-HT1A</subject><subject>Adult</subject><subject>Asymmetry</subject><subject>Auditory Perception - physiology</subject><subject>Brain</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - physiology</subject><subject>Brain asymmetry</subject><subject>Brain research</subject><subject>Carbon Radioisotopes - pharmacokinetics</subject><subject>Female</subject><subject>Females</subject><subject>Functional Laterality - physiology</subject><subject>Gender differences</subject><subject>Humans</subject><subject>Language</subject><subject>Lateralization</subject><subject>Male</subject><subject>Menstruation</subject><subject>Piperazines - pharmacokinetics</subject><subject>Plasma</subject><subject>Positron-Emission Tomography - methods</subject><subject>Pyridines - pharmacokinetics</subject><subject>Receptor, Serotonin, 5-HT1A - metabolism</subject><subject>Serotonin</subject><subject>Serotonin Antagonists - pharmacokinetics</subject><subject>Sex hormones</subject><subject>Studies</subject><subject>Testosterone</subject><subject>Tissue Distribution</subject><issn>1053-8119</issn><issn>1095-9572</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkU2L1TAUhoMozof-BQkI7lrPaZq0WY7D6AgXdDFu3IQ0PR1z6W2uSTow_npzvRcG3MwqgTznI-_DGEeoEVB93NYLrTH4nb2nugHoa8QahHjBzhG0rLTsmpeHuxRVj6jP2EVKWwDQ2Pav2RlqBNHo9pz93NhM0c7-j80-LDxMPP8iniiGHBa_VHjFIzna5xD56FOOflj_kX7hs13u17ICt5FsKtwD2ZlGPjzy7zd3b9iryc6J3p7OS_bj883d9W21-fbl6_XVpnKtwFz1Eok6ElpJMQ0AriMlBqWEBBKddEM7Eg2NBKFakNq6xk1j25aXsdFOO3HJPhz77mP4vVLKZueTo7lsR2FNRiktQYn2WbABoZsSXQHf_wduwxqX8gmDpVXXtyXTQvVHysWQUqTJ7GMxEh8NgjloMlvzpMkcNBlEUzSV0nenAeuwo_Gp8OSlAJ-OAJXgHjxFk5ynxdHoi41sxuCfn_IXDZ2oYA</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Fink, Martin</creator><creator>Wadsak, Wolfgang</creator><creator>Savli, Markus</creator><creator>Stein, Patrycja</creator><creator>Moser, Ulrike</creator><creator>Hahn, Andreas</creator><creator>Mien, Leonhard-Key</creator><creator>Kletter, Kurt</creator><creator>Mitterhauser, Markus</creator><creator>Kasper, Siegfried</creator><creator>Lanzenberger, Rupert</creator><general>Elsevier Inc</general><general>Elsevier Limited</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><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>20090401</creationdate><title>Lateralization of the serotonin-1A receptor distribution in language areas revealed by PET</title><author>Fink, Martin ; Wadsak, Wolfgang ; Savli, Markus ; Stein, Patrycja ; Moser, Ulrike ; Hahn, Andreas ; Mien, Leonhard-Key ; Kletter, Kurt ; Mitterhauser, Markus ; Kasper, Siegfried ; Lanzenberger, Rupert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-851ee7e39653fb00c7e63b66350e375cb4deeb250364059ac2cfd4475cd29c9c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>5-HT1A</topic><topic>Adult</topic><topic>Asymmetry</topic><topic>Auditory Perception - physiology</topic><topic>Brain</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - physiology</topic><topic>Brain asymmetry</topic><topic>Brain research</topic><topic>Carbon Radioisotopes - pharmacokinetics</topic><topic>Female</topic><topic>Females</topic><topic>Functional Laterality - physiology</topic><topic>Gender differences</topic><topic>Humans</topic><topic>Language</topic><topic>Lateralization</topic><topic>Male</topic><topic>Menstruation</topic><topic>Piperazines - pharmacokinetics</topic><topic>Plasma</topic><topic>Positron-Emission Tomography - methods</topic><topic>Pyridines - pharmacokinetics</topic><topic>Receptor, Serotonin, 5-HT1A - metabolism</topic><topic>Serotonin</topic><topic>Serotonin Antagonists - pharmacokinetics</topic><topic>Sex hormones</topic><topic>Studies</topic><topic>Testosterone</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fink, Martin</creatorcontrib><creatorcontrib>Wadsak, Wolfgang</creatorcontrib><creatorcontrib>Savli, Markus</creatorcontrib><creatorcontrib>Stein, Patrycja</creatorcontrib><creatorcontrib>Moser, Ulrike</creatorcontrib><creatorcontrib>Hahn, Andreas</creatorcontrib><creatorcontrib>Mien, Leonhard-Key</creatorcontrib><creatorcontrib>Kletter, Kurt</creatorcontrib><creatorcontrib>Mitterhauser, Markus</creatorcontrib><creatorcontrib>Kasper, Siegfried</creatorcontrib><creatorcontrib>Lanzenberger, Rupert</creatorcontrib><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>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>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Biological Science Database</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>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>NeuroImage (Orlando, Fla.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fink, Martin</au><au>Wadsak, Wolfgang</au><au>Savli, Markus</au><au>Stein, Patrycja</au><au>Moser, Ulrike</au><au>Hahn, Andreas</au><au>Mien, Leonhard-Key</au><au>Kletter, Kurt</au><au>Mitterhauser, Markus</au><au>Kasper, Siegfried</au><au>Lanzenberger, Rupert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lateralization of the serotonin-1A receptor distribution in language areas revealed by PET</atitle><jtitle>NeuroImage (Orlando, Fla.)</jtitle><addtitle>Neuroimage</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>45</volume><issue>2</issue><spage>598</spage><epage>605</epage><pages>598-605</pages><issn>1053-8119</issn><eissn>1095-9572</eissn><abstract>Lateralization is a well described aspect of the human brain. A plethora of morphological, cytological and functional studies describes hemispheric asymmetry in auditory and language areas. However, no study has reported cortical lateralization in the healthy human brain in vivo on the level of neurotransmitter receptors and in relation to functional organization so far. In this study, we assessed the distribution of the main inhibitory serotonergic receptor (the 5-HT1A receptor) and analyzed its regional binding with regard to hemisphere, sex and plasma levels of sex steroid hormones (testosterone, estradiol, progesterone). We quantified the 5-HT1A receptor binding potential by positron emission tomography (PET) using the highly selective and specific radioligand [carbonyl-11C]WAY-100635 and measured hormone levels in thirty-four (16 females, 18 males) healthy right-handed subjects. The obtained data were analyzed in an automated region of interest (ROI) based approach investigating 14 auditory, language and limbic areas. We found significantly higher 5-HT1A receptor binding in the superior and middle frontal gyri of the right hemisphere, the triangular and orbital parts of the inferior frontal gyrus, the supramarginal gyrus, the superior gyrus of the temporal pole and the middle temporal gyrus. Regions of the primary and secondary auditory cortex (Heschl's gyrus and superior temporal gyrus) and the Rolandic operculum displayed significantly higher receptor binding in the left hemisphere. 5-HT1A receptor binding was 1.8–2.9% higher in right frontal ROIs and 2–3.6% higher in left primary and secondary auditory regions. There was no hemispheric difference in 5-HT1A receptor binding in the hippocampus, amygdala, and insula. Post-hoc testing suggested that lateralization of 5-HT1A receptor binding differed between the sexes in the triangular part of the inferior frontal gyrus. For the first time, this PET study shows lateralization of the main inhibitory receptor of the serotonergic system in functionally asymmetric organized regions of the healthy human brain in vivo.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19103294</pmid><doi>10.1016/j.neuroimage.2008.11.033</doi><tpages>8</tpages></addata></record> |
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subjects | 5-HT1A Adult Asymmetry Auditory Perception - physiology Brain Brain - diagnostic imaging Brain - physiology Brain asymmetry Brain research Carbon Radioisotopes - pharmacokinetics Female Females Functional Laterality - physiology Gender differences Humans Language Lateralization Male Menstruation Piperazines - pharmacokinetics Plasma Positron-Emission Tomography - methods Pyridines - pharmacokinetics Receptor, Serotonin, 5-HT1A - metabolism Serotonin Serotonin Antagonists - pharmacokinetics Sex hormones Studies Testosterone Tissue Distribution |
title | Lateralization of the serotonin-1A receptor distribution in language areas revealed by PET |
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