Determination of [11C]PBR28 Binding Potential in vivo: A First Human TSPO Blocking Study
Positron emission tomography (PET) targeting the 18 kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed throughout the brain, and therefore a classical reference region approach cannot be used to estimate binding potential (BPND). Here, we used bl...
Saved in:
Published in | Journal of cerebral blood flow and metabolism Vol. 34; no. 6; pp. 989 - 994 |
---|---|
Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London, England
SAGE Publications
01.06.2014
Sage Publications Ltd Nature Publishing Group |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Positron emission tomography (PET) targeting the 18 kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed throughout the brain, and therefore a classical reference region approach cannot be used to estimate binding potential (BPND). Here, we used blockade of the TSPO radioligand [11C]PBR28 with the TSPO ligand XBD173, to determine the non-displaceable volume of distribution (VND), and hence estimate the BPND. A total of 26 healthy volunteers, 16 high-affinity binders (HABs) and 10 mixed affinity binders (MABs) underwent a [11C]PBR28 PET scan with arterial sampling. Six of the HABs received oral XBD173 (10 to 90 mg), 2 hours before a repeat scan. In XBD173-dosed subjects, VND was estimated via the occupancy plot. Values of BPND for all subjects were calculated using this VND estimate. Total volume of distribution (VT) of MABs (2.94 ± 0.31) was lower than VT of HABs (4.33 ± 0.29) (P<0.005). There was dose-dependent occupancy of TSPO by XBD173 (ED50 = 0.34 ± 0.13 mg/kg). The occupancy plot provided a VND estimate of 1.98 (1.69, 2.26). Based on these VND estimates, BPND for HABs is approximately twice that of MABs, consistent with predictions from in vitro data. Our estimates of [11C]PBR28 VND and hence BPND in the healthy human brain are consistent with in vitro predictions. XBD173 blockade provides a practical means of estimating VND for TSPO targeting radioligands. |
---|---|
AbstractList | Positron emission tomography (PET) targeting the 18 kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed throughout the brain, and therefore a classical reference region approach cannot be used to estimate binding potential (BPND). Here, we used blockade of the TSPO radioligand [(11)C]PBR28 with the TSPO ligand XBD173, to determine the non-displaceable volume of distribution (VND), and hence estimate the BPND. A total of 26 healthy volunteers, 16 high-affinity binders (HABs) and 10 mixed affinity binders (MABs) underwent a [(11)C]PBR28 PET scan with arterial sampling. Six of the HABs received oral XBD173 (10 to 90 mg), 2 hours before a repeat scan. In XBD173-dosed subjects, VND was estimated via the occupancy plot. Values of BPND for all subjects were calculated using this VND estimate. Total volume of distribution (VT) of MABs (2.94±0.31) was lower than VT of HABs (4.33±0.29) (P<0.005). There was dose-dependent occupancy of TSPO by XBD173 (ED50=0.34±0.13 mg/kg). The occupancy plot provided a VND estimate of 1.98 (1.69, 2.26). Based on these VND estimates, BPND for HABs is approximately twice that of MABs, consistent with predictions from in vitro data. Our estimates of [(11)C]PBR28 VND and hence BPND in the healthy human brain are consistent with in vitro predictions. XBD173 blockade provides a practical means of estimating VND for TSPO targeting radioligands. Positron emission tomography (PET) targeting the 18 kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed throughout the brain, and therefore a classical reference region approach cannot be used to estimate binding potential (BPND). Here, we used blockade of the TSPO radioligand [11C]PBR28 with the TSPO ligand XBD173, to determine the non-displaceable volume of distribution (VND), and hence estimate the BPND. A total of 26 healthy volunteers, 16 high-affinity binders (HABs) and 10 mixed affinity binders (MABs) underwent a [11C]PBR28 PET scan with arterial sampling. Six of the HABs received oral XBD173 (10 to 90 mg), 2 hours before a repeat scan. In XBD173-dosed subjects, VND was estimated via the occupancy plot. Values of BPND for all subjects were calculated using this VND estimate. Total volume of distribution (VT) of MABs (2.94 ± 0.31) was lower than VT of HABs (4.33 ± 0.29) (P<0.005). There was dose-dependent occupancy of TSPO by XBD173 (ED50 = 0.34 ± 0.13 mg/kg). The occupancy plot provided a VND estimate of 1.98 (1.69, 2.26). Based on these VND estimates, BPND for HABs is approximately twice that of MABs, consistent with predictions from in vitro data. Our estimates of [11C]PBR28 VND and hence BPND in the healthy human brain are consistent with in vitro predictions. XBD173 blockade provides a practical means of estimating VND for TSPO targeting radioligands. Positron emission tomography (PET) targeting the 18 kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed throughout the brain, and therefore a classical reference region approach cannot be used to estimate binding potential ( BP ND ). Here, we used blockade of the TSPO radioligand [ 11 C]PBR28 with the TSPO ligand XBD173, to determine the non-displaceable volume of distribution ( V ND ), and hence estimate the BP ND . A total of 26 healthy volunteers, 16 high-affinity binders (HABs) and 10 mixed affinity binders (MABs) underwent a [ 11 C]PBR28 PET scan with arterial sampling. Six of the HABs received oral XBD173 (10 to 90 mg), 2 hours before a repeat scan. In XBD173-dosed subjects, V ND was estimated via the occupancy plot. Values of BP ND for all subjects were calculated using this V ND estimate. Total volume of distribution ( V T ) of MABs (2.94 ± 0.31) was lower than V T of HABs (4.33 ± 0.29) ( P<0.005). There was dose-dependent occupancy of TSPO by XBD173 (ED50 = 0.34 ± 0.13 mg/kg). The occupancy plot provided a V ND estimate of 1.98 (1.69, 2.26). Based on these V ND estimates, BP ND for HABs is approximately twice that of MABs, consistent with predictions from in vitro data. Our estimates of [ 11 C]PBR28 V ND and hence BP ND in the healthy human brain are consistent with in vitro predictions. XBD173 blockade provides a practical means of estimating V ND for TSPO targeting radioligands. Positron emission tomography (PET) targeting the 18 kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed throughout the brain, and therefore a classical reference region approach cannot be used to estimate binding potential (BP sub(ND)). Here, we used blockade of the TSPO radioligand [ super(11)C]PBR28 with the TSPO ligand XBD173, to determine the non-displaceable volume of distribution (V sub(ND)), and hence estimate the BP sub(ND). A total of 26 healthy volunteers, 16 high-affinity binders (HABs) and 10 mixed affinity binders (MABs) underwent a [ super(11)C]PBR28 PET scan with arterial sampling. Six of the HABs received oral XBD173 (10 to 90 mg), 2 hours before a repeat scan. In XBD173-dosed subjects, V sub(ND) was estimated via the occupancy plot. Values of BP sub(ND) for all subjects were calculated using this V sub(ND) estimate. Total volume of distribution (V sub(T)) of MABs (2.94 plus or minus 0.31) was lower than V sub(T) of HABs (4.33 plus or minus 0.29) (P<0.005). There was dose-dependent occupancy of TSPO by XBD173 (ED50=0.34 plus or minus 0.13 mg/kg). The occupancy plot provided a V sub(ND) estimate of 1.98 (1.69, 2.26). Based on these V sub(ND) estimates, BP sub(ND) for HABs is approximately twice that of MABs, consistent with predictions from in vitro data. Our estimates of [ super(11)C]PBR28 V sub(ND) and hence BP sub(ND) in the healthy human brain are consistent with in vitro predictions. XBD173 blockade provides a practical means of estimating V sub(ND) for TSPO targeting radioligands. Positron emission tomography (PET) targeting the 18 kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed throughout the brain, and therefore a classical reference region approach cannot be used to estimate binding potential ( BP ND ). Here, we used blockade of the TSPO radioligand [ 11 C]PBR28 with the TSPO ligand XBD173, to determine the non-displaceable volume of distribution ( V ND ), and hence estimate the BP ND . A total of 26 healthy volunteers, 16 high-affinity binders (HABs) and 10 mixed affinity binders (MABs) underwent a [ 11 C]PBR28 PET scan with arterial sampling. Six of the HABs received oral XBD173 (10 to 90 mg), 2 hours before a repeat scan. In XBD173-dosed subjects, V ND was estimated via the occupancy plot. Values of BP ND for all subjects were calculated using this V ND estimate. Total volume of distribution ( V T ) of MABs (2.94±0.31) was lower than V T of HABs (4.33±0.29) ( P <0.005). There was dose-dependent occupancy of TSPO by XBD173 (ED50=0.34±0.13 mg/kg). The occupancy plot provided a V ND estimate of 1.98 (1.69, 2.26). Based on these V ND estimates, BP ND for HABs is approximately twice that of MABs, consistent with predictions from in vitro data. Our estimates of [ 11 C]PBR28 V ND and hence BP ND in the healthy human brain are consistent with in vitro predictions. XBD173 blockade provides a practical means of estimating V ND for TSPO targeting radioligands. Positron emission tomography (PET) targeting the 18kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed throughout the brain, and therefore a classical reference region approach cannot be used to estimate binding potential (BPND). Here, we used blockade of the TSPO radioligand [(11)C]PBR28 with the TSPO ligand XBD173, to determine the non-displaceable volume of distribution (VND), and hence estimate the BPND. A total of 26 healthy volunteers, 16 high-affinity binders (HABs) and 10 mixed affinity binders (MABs) underwent a [(11)C]PBR28 PET scan with arterial sampling. Six of the HABs received oral XBD173 (10 to 90mg), 2hours before a repeat scan. In XBD173-dosed subjects, VND was estimated via the occupancy plot. Values of BPND for all subjects were calculated using this VND estimate. Total volume of distribution (VT) of MABs (2.94±0.31) was lower than VT of HABs (4.33±0.29) (P<0.005). There was dose-dependent occupancy of TSPO by XBD173 (ED50=0.34±0.13mg/kg). The occupancy plot provided a VND estimate of 1.98 (1.69, 2.26). Based on these VND estimates, BPND for HABs is approximately twice that of MABs, consistent with predictions from in vitro data. Our estimates of [(11)C]PBR28 VND and hence BPND in the healthy human brain are consistent with in vitro predictions. XBD173 blockade provides a practical means of estimating VND for TSPO targeting radioligands. |
Author | Colasanti, Alessandro Barletta, Julien Kamalakaran, Aruloly Matthews, Paul M Gunn, Roger N Passchier, Jan Ramada-Magalhaes, Joaquim Nutt, David J Rabiner, Eugenii A Kalk, Nicola J Owen, David R Libri, Vincenzo Dimber, Rahul Kalogiannopoulou, Dimitra Lewis, Yvonne L Guo, Qi |
Author_xml | – sequence: 1 givenname: David R surname: Owen fullname: Owen, David R email: d.owen@imperial.ac.uk – sequence: 2 givenname: Qi surname: Guo fullname: Guo, Qi – sequence: 3 givenname: Nicola J surname: Kalk fullname: Kalk, Nicola J – sequence: 4 givenname: Alessandro surname: Colasanti fullname: Colasanti, Alessandro – sequence: 5 givenname: Dimitra surname: Kalogiannopoulou fullname: Kalogiannopoulou, Dimitra – sequence: 6 givenname: Rahul surname: Dimber fullname: Dimber, Rahul – sequence: 7 givenname: Yvonne L surname: Lewis fullname: Lewis, Yvonne L – sequence: 8 givenname: Vincenzo surname: Libri fullname: Libri, Vincenzo – sequence: 9 givenname: Julien surname: Barletta fullname: Barletta, Julien – sequence: 10 givenname: Joaquim surname: Ramada-Magalhaes fullname: Ramada-Magalhaes, Joaquim – sequence: 11 givenname: Aruloly surname: Kamalakaran fullname: Kamalakaran, Aruloly – sequence: 12 givenname: David J surname: Nutt fullname: Nutt, David J – sequence: 13 givenname: Jan surname: Passchier fullname: Passchier, Jan – sequence: 14 givenname: Paul M surname: Matthews fullname: Matthews, Paul M – sequence: 15 givenname: Roger N surname: Gunn fullname: Gunn, Roger N – sequence: 16 givenname: Eugenii A surname: Rabiner fullname: Rabiner, Eugenii A |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24643083$$D View this record in MEDLINE/PubMed |
BookMark | eNp1kd1rFDEUxYNU7Lb66KsEfBFh1nzPjA-F7mqtUOhiKxREQibJrFlnkjrJLPS_N9OtpRZ9Cpf87uGcew7Ang_eAvASozlGtHq30U3bzwnCbM7EEzDDnNdFibDYAzNESlyIsrraBwcxbhBCFeX8GdgnTDCahxm4-mCTHXrnVXLBw9DCbxgvv68WX0gFF84b59dwFZL1yakOOg-3bhvew2N44oaY4OnYKw8vL1bncNEF_XPCL9Jobp6Dp63qon1x9x6CrycfL5enxdn5p8_L47NCcyxSUXJBdKOM0UKYttGobtqKG6YMamlJaqIZzyMnDa5RRUxZYtRwbKmgbd02gh6Co53u9dj01uhsdFCdvB5cr4YbGZSTf_9490Ouw1YyxBFhNAu8uRMYwq_RxiR7F7XtOuVtGKPEnLKKlByxjL5-hG7COPgcb6Iw4jinydSrh47urfw5egaKHaCHEONg23sEIzmVKm9LlVOpkk0R6SNeu3TbVw7kuv9uvd1tRbW2D4z-E_4NIaeyeg |
CitedBy_id | crossref_primary_10_1073_pnas_1511003112 crossref_primary_10_1212_WNL_0000000000002485 crossref_primary_10_1111_bcp_15392 crossref_primary_10_1038_s41590_020_00812_1 crossref_primary_10_1177_0271678X15610585 crossref_primary_10_3390_diagnostics13061029 crossref_primary_10_1186_s13550_017_0334_8 crossref_primary_10_1007_s11307_020_01575_9 crossref_primary_10_2967_jnumed_116_178996 crossref_primary_10_1186_s41181_019_0058_3 crossref_primary_10_1038_s41467_020_15930_5 crossref_primary_10_1007_s40336_015_0155_6 crossref_primary_10_1002_syn_21970 crossref_primary_10_1038_s41582_019_0240_y crossref_primary_10_1002_glia_22978 crossref_primary_10_1016_j_biopha_2023_115582 crossref_primary_10_2967_jnumed_120_243717 crossref_primary_10_1007_s00259_021_05327_x crossref_primary_10_1007_s40336_015_0140_0 crossref_primary_10_1016_j_biopsych_2018_02_1171 crossref_primary_10_23736_S1824_4785_18_03105_9 crossref_primary_10_1016_j_dadm_2019_09_004 crossref_primary_10_1007_s40336_015_0141_z crossref_primary_10_1038_s41531_018_0057_1 crossref_primary_10_2967_jnumed_115_162461 crossref_primary_10_1177_0271678X19858003 crossref_primary_10_1073_pnas_2406005121 crossref_primary_10_1016_j_pbb_2019_01_007 crossref_primary_10_1093_brain_awy188 crossref_primary_10_1002_acn3_50837 crossref_primary_10_1016_j_neuroimage_2017_12_002 crossref_primary_10_1016_j_bbadis_2015_11_011 crossref_primary_10_1007_s13365_024_01200_3 crossref_primary_10_1093_brain_awae234 crossref_primary_10_2967_jnumed_117_202200 crossref_primary_10_1093_braincomms_fcad084 crossref_primary_10_2967_jnumed_114_146027 crossref_primary_10_1002_hbm_26491 crossref_primary_10_1186_s13550_017_0271_6 crossref_primary_10_1093_cei_uxab013 crossref_primary_10_3389_fmed_2022_812270 crossref_primary_10_1177_0271678X231205661 crossref_primary_10_1093_brain_awv184 crossref_primary_10_1016_j_ddtec_2017_11_009 crossref_primary_10_2967_jnumed_117_204453 crossref_primary_10_1038_jcbfm_2015_54 crossref_primary_10_1007_s00429_014_0970_y crossref_primary_10_1176_appi_ajp_2015_14101358 crossref_primary_10_2967_jnumed_115_156083 crossref_primary_10_3805_eands_12_40 crossref_primary_10_1016_j_neuroimage_2018_11_020 crossref_primary_10_4236_wjns_2018_81006 crossref_primary_10_1523_JNEUROSCI_2070_18_2019 crossref_primary_10_1016_j_schres_2017_08_063 crossref_primary_10_1186_s40658_021_00381_8 crossref_primary_10_1124_jpet_116_238568 crossref_primary_10_1109_TBME_2018_2874308 crossref_primary_10_1517_17460441_2015_1032240 crossref_primary_10_1002_syn_21890 crossref_primary_10_1055_s_0040_1713607 crossref_primary_10_1007_s40336_015_0138_7 crossref_primary_10_1186_s13550_016_0226_3 crossref_primary_10_1007_s11307_019_01323_8 crossref_primary_10_1007_s00259_015_3043_4 crossref_primary_10_1007_s00259_019_04349_w crossref_primary_10_1177_0271678X17748786 crossref_primary_10_1016_j_neuroimage_2022_119031 crossref_primary_10_1007_s00259_019_04403_7 crossref_primary_10_3389_fneur_2020_541377 crossref_primary_10_3390_diagnostics12051161 crossref_primary_10_1177_0271678X18771250 crossref_primary_10_1007_s00259_014_2955_8 crossref_primary_10_1038_s41531_024_00708_z crossref_primary_10_1097_QAI_0000000000002435 crossref_primary_10_2967_jnumed_115_165019 crossref_primary_10_1111_ejn_15613 crossref_primary_10_1016_j_bbi_2016_01_019 crossref_primary_10_1186_s40658_023_00591_2 crossref_primary_10_1017_S003329171800421X crossref_primary_10_1007_s11910_020_1025_9 crossref_primary_10_3389_fnimg_2023_1142463 crossref_primary_10_1053_j_semnuclmed_2015_09_001 crossref_primary_10_2967_jnumed_116_187161 crossref_primary_10_1007_s40336_015_0137_8 crossref_primary_10_1093_brain_awx339 crossref_primary_10_1007_s11481_018_9823_4 crossref_primary_10_1159_000499621 crossref_primary_10_1053_j_semnuclmed_2017_12_005 crossref_primary_10_1007_s00259_016_3444_z crossref_primary_10_1038_mp_2016_247 crossref_primary_10_1038_mp_2017_10 crossref_primary_10_1177_0271678X17699223 crossref_primary_10_1007_s00259_021_05309_z crossref_primary_10_1016_j_phrs_2023_106681 crossref_primary_10_1007_s11307_019_01433_3 crossref_primary_10_1186_s13550_020_00736_9 crossref_primary_10_1007_s00259_015_3149_8 |
Cites_doi | 10.1126/science.1175055 10.1093/brain/123.11.2321 10.2967/jnumed.113.121020 10.1002/syn.20884 10.1111/j.1365-2990.2008.01006.x 10.1212/01.wnl.0000222734.56412.17 10.1038/jcbfm.2011.147 10.1016/j.neuroimage.2010.06.044 10.2967/jnumed.112.118885 10.1038/jcbfm.2012.46 10.1016/S0969-8051(00)00115-3 10.1007/s00259-008-0908-9 10.1093/brain/awh161 10.1038/jcbfm.2009.190 10.1038/sj.jcbfm.9600493 10.1016/j.neuroimage.2007.11.011 10.1016/S0969-8051(00)00125-6 10.1038/jcbfm.2010.63 10.1016/j.neuroimage.2004.09.034 10.1016/j.nbd.2005.08.002 10.2967/jnumed.110.079459 10.1038/jcbfm.2012.131 |
ContentType | Journal Article |
Copyright | 2014 ISCBFM Copyright Nature Publishing Group Jun 2014 Copyright © 2014 International Society for Cerebral Blood Flow & Metabolism, Inc. 2014 International Society for Cerebral Blood Flow & Metabolism, Inc. |
Copyright_xml | – notice: 2014 ISCBFM – notice: Copyright Nature Publishing Group Jun 2014 – notice: Copyright © 2014 International Society for Cerebral Blood Flow & Metabolism, Inc. 2014 International Society for Cerebral Blood Flow & Metabolism, Inc. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7X7 7XB 88A 88E 8AO 8FE 8FH 8FI 8FJ 8FK ABUWG AFKRA AZQEC BBNVY BENPR BHPHI CCPQU DWQXO FYUFA GHDGH GNUQQ HCIFZ K9. LK8 M0S M1P M7P PHGZM PHGZT PJZUB PKEHL PPXIY PQEST PQGLB PQQKQ PQUKI PRINS 7TK 5PM |
DOI | 10.1038/jcbfm.2014.46 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Health & Medical Collection ProQuest Central (purchase pre-March 2016) Biology Database (Alumni Edition) Medical Database (Alumni Edition) ProQuest Pharma Collection ProQuest SciTech Collection ProQuest Natural Science Collection Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central Essentials Biological Science Collection ProQuest Central Natural Science Collection ProQuest One Community College ProQuest Central Korea Proquest Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Central Student SciTech Premium Collection ProQuest Health & Medical Complete (Alumni) ProQuest Biological Science Collection ProQuest Health & Medical Collection Medical Database Biological Science Database ProQuest Central Premium ProQuest One Academic (New) ProQuest Health & Medical Research Collection ProQuest One Academic Middle East (New) ProQuest One Health & Nursing ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Applied & Life Sciences ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China Neurosciences Abstracts PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Central Student ProQuest One Academic Middle East (New) ProQuest Central Essentials ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) SciTech Premium Collection ProQuest One Community College ProQuest One Health & Nursing ProQuest Natural Science Collection ProQuest Pharma Collection ProQuest Central China ProQuest Biology Journals (Alumni Edition) ProQuest Central ProQuest One Applied & Life Sciences ProQuest Health & Medical Research Collection Health Research Premium Collection Health and Medicine Complete (Alumni Edition) Natural Science Collection ProQuest Central Korea Health & Medical Research Collection Biological Science Collection ProQuest Central (New) ProQuest Medical Library (Alumni) ProQuest Biological Science Collection ProQuest One Academic Eastern Edition ProQuest Hospital Collection Health Research Premium Collection (Alumni) Biological Science Database ProQuest SciTech Collection ProQuest Hospital Collection (Alumni) ProQuest Health & Medical Complete ProQuest Medical Library ProQuest One Academic UKI Edition ProQuest One Academic ProQuest One Academic (New) ProQuest Central (Alumni) Neurosciences Abstracts |
DatabaseTitleList | MEDLINE CrossRef Neurosciences Abstracts ProQuest Central Student |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: BENPR name: ProQuest Central url: https://www.proquest.com/central sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Anatomy & Physiology Chemistry |
DocumentTitleAlternate | TSPO blockade study |
EISSN | 1559-7016 |
EndPage | 994 |
ExternalDocumentID | PMC4050243 3321669981 24643083 10_1038_jcbfm_2014_46 10.1038_jcbfm.2014.46 |
Genre | Clinical Trial Journal Article |
GrantInformation_xml | – fundername: Medical Research Council grantid: G0900897 – fundername: Parkinson's UK grantid: G-0909 – fundername: Medical Research Council grantid: MR/L01307X/1 |
GroupedDBID | --- -Q- -TM .55 .GJ 0R~ 29K 2WC 36B 39C 3O- 4.4 53G 54M 5GY 5RE 5VS 70F 7X7 88E 8AO 8FE 8FH 8FI 8FJ 8R4 8R5 AABMB AACKU AACMV AADUE AAEWN AAGGD AAGMC AAJIQ AAJPV AAKGS AANSI AAPEO AAQGT AAQXH AAQXI AARDL AARIX AATAA AATBZ AAUAS AAVDI AAXOT AAYTG AAZBJ ABAWP ABAWZ ABCCA ABCJG ABDWY ABEIX ABFWQ ABHKI ABJNI ABJZC ABKRH ABLUO ABNCE ABPGX ABPNF ABQKF ABQNX ABQXT ABRHV ABUJY ABUWG ABVFX ABXGC ABYTW ACARO ACDSZ ACDXX ACFEJ ACFMA ACGBL ACGFO ACGFS ACGZU ACJER ACJTF ACLFY ACLHI ACNXM ACOFE ACOXC ACPRK ACROE ACSIQ ACUAV ACUIR ACXKE ACXMB ADBBV ADEBD ADEIA ADMPF ADNON ADRRZ ADTBJ ADUKL ADVBO ADZZY AECGH AENEX AEPTA AEQLS AESZF AEUHG AEWDL AEWHI AEXFG AEXNY AFEET AFFNX AFFZS AFKRA AFKRG AFMOU AFOSN AFQAA AFUIA AFVCE AGHKR AGKLV AGNHF AGPXR AGWFA AHDMH AHMBA AIGRN AJABX AJEFB AJMMQ AJSCY AJUZI AJXAJ AJXGE ALIPV ALKWR ALMA_UNASSIGNED_HOLDINGS AMCVQ ANDLU AOIJS ARTOV AUTPY AYAKG B8M BAWUL BBNVY BBRGL BDDNI BENPR BHPHI BKIIM BKSCU BPACV BPHCQ BSEHC BVXVI BWJAD C45 CAG CBRKF CCPQU CDWPY CFDXU COF CORYS CQQTX CS3 CUTAK D-I DC- DC. DIK DOPDO DV7 E3Z EBS EE. EJD EMOBN F5P FHBDP FYUFA GROUPED_SAGE_PREMIER_JOURNAL_COLLECTION GX1 H13 HCIFZ HMCUK HYE HZ~ J8X JSO K.F KQ8 LK8 M1P M7P O9- OK1 OVD P2P P6G PHGZM PHGZT PQQKQ PROAC PSQYO Q1R Q2X RNS RNTTT ROL RPM SASJQ SAUOL SCNPE SFC SHG SPQ SPV TEORI TR2 UKHRP W2D X7M YFH YOC ZGI ZONMY ZPPRI ZRKOI ZSSAH ZXP AAYXX AJGYC CITATION AAEJI AAPII AJVBE CGR CUY CVF ECM EIF NPM PJZUB PPXIY PQGLB 3V. 7XB 88A 8FK AJHME AZQEC DWQXO GNUQQ K9. PKEHL PQEST PQUKI PRINS 7TK 5PM |
ID | FETCH-LOGICAL-c516t-7562cbaddc66dfbc09bf85d4ad0f37292c455d452b19082d7710b51e363f9fb63 |
IEDL.DBID | 7X7 |
ISSN | 0271-678X |
IngestDate | Thu Aug 21 14:14:00 EDT 2025 Fri Jul 11 10:55:56 EDT 2025 Wed Aug 13 11:09:22 EDT 2025 Mon Jul 21 05:53:15 EDT 2025 Tue Jul 01 05:20:04 EDT 2025 Thu Apr 24 22:51:39 EDT 2025 Tue Jun 17 22:39:19 EDT 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 6 |
Keywords | [11C]PBR28 TSPO specific binding rs6971 polymorphism emapunil XBD173 |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c516t-7562cbaddc66dfbc09bf85d4ad0f37292c455d452b19082d7710b51e363f9fb63 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
OpenAccessLink | https://journals.sagepub.com/doi/pdf/10.1038/jcbfm.2014.46 |
PMID | 24643083 |
PQID | 1531051562 |
PQPubID | 31524 |
PageCount | 6 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_4050243 proquest_miscellaneous_1534827504 proquest_journals_1531051562 pubmed_primary_24643083 crossref_primary_10_1038_jcbfm_2014_46 crossref_citationtrail_10_1038_jcbfm_2014_46 sage_journals_10_1038_jcbfm_2014_46 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2014-06-01 |
PublicationDateYYYYMMDD | 2014-06-01 |
PublicationDate_xml | – month: 06 year: 2014 text: 2014-06-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | London, England |
PublicationPlace_xml | – name: London, England – name: United States – name: London |
PublicationTitle | Journal of cerebral blood flow and metabolism |
PublicationTitleAlternate | J Cereb Blood Flow Metab |
PublicationYear | 2014 |
Publisher | SAGE Publications Sage Publications Ltd Nature Publishing Group |
Publisher_xml | – name: SAGE Publications – name: Sage Publications Ltd – name: Nature Publishing Group |
References | Innis, Cunningham, Delforge, Fujita, Gjedde, Gunn 2007; 27 Gunn, Lammertsma, Grasby 2000; 27 Yoder, Nho, Risacher, Kim, Shen, Saykin 2013; 54 Owen, Lewis, Reynolds, Rupprecht, Eser, Wilkins 2011; 65 Gerhard, Schwarz, Myers, Wise, Banati 2005; 24 Hilton, Yokoi, Dannals, Ravert, Szabo, Wong 2000; 27 Cunningham, Rabiner, Slifstein, Lamelle, Gunn 2010; 30 Rupprecht, Rammes, Eser, Baghai, Schule, Nothdurfter 2009; 325 Chen, Baidoo, Verina, Guilarte 2004; 127 Pavese, Gerhard, Tai, Ho, Turkheimer, Barker 2006; 66 Kreisl, Jenko, Hines, Lyoo, Corona, Morse 2013; 33 Owen, Yeo, Gunn, Song, Wadsworth, Lewis 2012; 32 Turkheimer, Edison, Pavese, Roncaroli, Anderson, Hammers 2007; 48 Banati, Newcombe, Gunn, Cagnin, Turkheimer, Heppner 2000; 123 Gerhard, Pavese, Hotton, Turkheimer, Es, Hammers 2006; 21 Guo, Colasanti, Owen, Onega, Kamalakaran, Bennacef 2013; 54 Mizrahi, Rusjan, Kennedy, Pollock, Mulsant, Suridjan 2012; 32 Tziortzi, Searle, Tzimopoulou, Salinas, Beaver, Jenkinson 2011; 54 Owen, Howell, Tang, Wells, Bennacef, Bergstrom 2010; 30 Cosenza-Nashat, Zhao, Suh, Morgan, Natividad, Morgello 2009; 35 Owen, Gunn, Rabiner, Bennacef, Fujita, Kreisl 2011; 52 Fujita, Imaizumi, Zoghbi, Fujimura, Farris, Suhara 2008; 40 Chauveau, Boutin, Van, Dolle, Tavitian 2008; 35 bibr18-jcbfm.2014.46 bibr4-jcbfm.2014.46 bibr12-jcbfm.2014.46 bibr20-jcbfm.2014.46 bibr13-jcbfm.2014.46 bibr3-jcbfm.2014.46 bibr17-jcbfm.2014.46 bibr14-jcbfm.2014.46 bibr8-jcbfm.2014.46 bibr16-jcbfm.2014.46 bibr21-jcbfm.2014.46 bibr9-jcbfm.2014.46 bibr1-jcbfm.2014.46 bibr15-jcbfm.2014.46 bibr6-jcbfm.2014.46 bibr2-jcbfm.2014.46 bibr7-jcbfm.2014.46 bibr23-jcbfm.2014.46 bibr5-jcbfm.2014.46 bibr11-jcbfm.2014.46 Turkheimer FE (bibr22-jcbfm.2014.46) 2007; 48 bibr10-jcbfm.2014.46 bibr19-jcbfm.2014.46 |
References_xml | – volume: 54 start-page: 1320 year: 2013 end-page: 1322 article-title: Influence of TSPO genotype on 11C-PBR28 standardized uptake values publication-title: J Nucl Med – volume: 27 start-page: 1533 year: 2007 end-page: 1539 article-title: Consensus nomenclature for in vivo imaging of reversibly binding radioligands publication-title: J Cereb Blood Flow Metab – volume: 35 start-page: 306 year: 2009 end-page: 328 article-title: Expression of the translocator protein of 18kDa by microglia, macrophages and astrocytes based on immunohistochemical localization in abnormal human brain publication-title: Neuropathol Appl Neurobiol – volume: 52 start-page: 24 year: 2011 end-page: 32 article-title: Mixed-affinity binding in humans with 18-kDa translocator protein ligands publication-title: J Nucl Med – volume: 33 start-page: 53 year: 2013 end-page: 58 article-title: A genetic polymorphism for translocator protein 18kDa affects both in vitro and in vivo radioligand binding in human brain to this putative biomarker of neuroinflammation publication-title: J Cereb Blood Flow Metab – volume: 27 start-page: 477 year: 2000 end-page: 482 article-title: Quantitative analysis of [carbonyl-(11)C]WAY-100635 PET studies publication-title: Nucl Med Biol – volume: 30 start-page: 46 year: 2010 end-page: 50 article-title: Measuring drug occupancy in the absence of a reference region: the Lassen plot re-visited publication-title: J Cereb Blood Flow Metab – volume: 27 start-page: 627 year: 2000 end-page: 630 article-title: Column-switching HPLC for the analysis of plasma in PET imaging studies publication-title: Nucl Med Biol – volume: 54 start-page: 1915 year: 2013 end-page: 1923 article-title: Quantification of the specific TSPO signal of [18F]PBR111 in healthy humans: a genetic polymorphism effect on in vivo binding publication-title: JNM – volume: 21 start-page: 404 year: 2006 end-page: 412 article-title: In vivo imaging of microglial activation with [11C](R)-PK11195 PET in idiopathic Parkinson's disease publication-title: Neurobiol Dis – volume: 66 start-page: 1638 year: 2006 end-page: 1643 article-title: Microglial activation correlates with severity in Huntington disease: a clinical and PET study publication-title: Neurology – volume: 32 start-page: 968 year: 2012 end-page: 972 article-title: Translocator protein (18 kDa) polymorphism (rs6971) explains in vivo brain binding affinity of the PET radioligand [(18)F]-FEPPA publication-title: J Cereb Blood Flow Metab – volume: 40 start-page: 43 year: 2008 end-page: 52 article-title: Kinetic analysis in healthy humans of a novel positron emission tomography radioligand to image the peripheral benzodiazepine receptor, a potential biomarker for inflammation publication-title: Neuroimage – volume: 32 start-page: 1 year: 2012 end-page: 5 article-title: An 18-kDa translocator protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28 publication-title: J Cereb Blood Flow Metab – volume: 30 start-page: 1608 year: 2010 end-page: 1618 article-title: Two binding sites for [(3)H]PBR28 in human brain: implications for TSPO PET imaging of neuroinflammation publication-title: J Cereb Blood Flow Metab – volume: 325 start-page: 490 year: 2009 end-page: 493 article-title: Translocator protein (18kD) as target for anxiolytics without benzodiazepine-like side effects publication-title: Science – volume: 123 start-page: 2321 year: 2000 end-page: 2337 article-title: The peripheral benzodiazepine binding site in the brain in multiple sclerosis: quantitative in vivo imaging of microglia as a measure of disease activity publication-title: Brain – volume: 24 start-page: 591 year: 2005 end-page: 595 article-title: Evolution of microglial activation in patients after ischemic stroke: a [11C](R)-PK11195 PET study publication-title: Neuroimage – volume: 65 start-page: 257 year: 2011 end-page: 259 article-title: Variation in binding affinity of the novel anxiolytic XBD173 for the 18 kDa translocator protein in human brain publication-title: Synapse – volume: 127 start-page: 1379 year: 2004 end-page: 1392 article-title: Peripheral benzodiazepine receptor imaging in CNS demyelination: functional implications of anatomical and cellular localization publication-title: Brain – volume: 48 start-page: 158 year: 2007 end-page: 167 article-title: Reference and target region modeling of [11C]-(R)-PK11195 brain studies publication-title: J Nucl Med – volume: 54 start-page: 264 year: 2011 end-page: 277 article-title: Imaging dopamine receptors in humans with [11C]-(+)-PHNO: dissection of D3 signal and anatomy publication-title: Neuroimage – volume: 35 start-page: 2304 year: 2008 end-page: 2319 article-title: Nuclear imaging of neuroinflammation: a comprehensive review of [11C]PK11195 challengers publication-title: Eur J Nucl Med Mol Imaging – ident: bibr16-jcbfm.2014.46 doi: 10.1126/science.1175055 – ident: bibr2-jcbfm.2014.46 doi: 10.1093/brain/123.11.2321 – ident: bibr10-jcbfm.2014.46 doi: 10.2967/jnumed.113.121020 – ident: bibr23-jcbfm.2014.46 doi: 10.1002/syn.20884 – ident: bibr1-jcbfm.2014.46 doi: 10.1111/j.1365-2990.2008.01006.x – ident: bibr4-jcbfm.2014.46 doi: 10.1212/01.wnl.0000222734.56412.17 – ident: bibr9-jcbfm.2014.46 doi: 10.1038/jcbfm.2011.147 – ident: bibr18-jcbfm.2014.46 doi: 10.1016/j.neuroimage.2010.06.044 – ident: bibr11-jcbfm.2014.46 doi: 10.2967/jnumed.112.118885 – ident: bibr12-jcbfm.2014.46 doi: 10.1038/jcbfm.2012.46 – ident: bibr20-jcbfm.2014.46 doi: 10.1016/S0969-8051(00)00115-3 – ident: bibr6-jcbfm.2014.46 doi: 10.1007/s00259-008-0908-9 – ident: bibr15-jcbfm.2014.46 doi: 10.1093/brain/awh161 – ident: bibr21-jcbfm.2014.46 doi: 10.1038/jcbfm.2009.190 – ident: bibr14-jcbfm.2014.46 doi: 10.1038/sj.jcbfm.9600493 – ident: bibr19-jcbfm.2014.46 doi: 10.1016/j.neuroimage.2007.11.011 – ident: bibr17-jcbfm.2014.46 doi: 10.1016/S0969-8051(00)00125-6 – ident: bibr7-jcbfm.2014.46 doi: 10.1038/jcbfm.2010.63 – ident: bibr5-jcbfm.2014.46 doi: 10.1016/j.neuroimage.2004.09.034 – ident: bibr3-jcbfm.2014.46 doi: 10.1016/j.nbd.2005.08.002 – ident: bibr8-jcbfm.2014.46 doi: 10.2967/jnumed.110.079459 – volume: 48 start-page: 158 year: 2007 ident: bibr22-jcbfm.2014.46 publication-title: J Nucl Med – ident: bibr13-jcbfm.2014.46 doi: 10.1038/jcbfm.2012.131 |
SSID | ssj0008355 |
Score | 2.4587183 |
Snippet | Positron emission tomography (PET) targeting the 18 kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed... Positron emission tomography (PET) targeting the 18 kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed... Positron emission tomography (PET) targeting the 18kDa translocator protein (TSPO) is used to quantify neuroinflammation. Translocator protein is expressed... |
SourceID | pubmedcentral proquest pubmed crossref sage |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 989 |
SubjectTerms | Acetamides - administration & dosage Adult Brain - diagnostic imaging Brain - metabolism Carbon Isotopes - administration & dosage Dose-Response Relationship, Drug Drug Delivery Systems Female Humans Male Original Positron-Emission Tomography Purines - administration & dosage Pyridines - administration & dosage Radiography Receptors, GABA - metabolism |
Title | Determination of [11C]PBR28 Binding Potential in vivo: A First Human TSPO Blocking Study |
URI | https://journals.sagepub.com/doi/full/10.1038/jcbfm.2014.46 https://www.ncbi.nlm.nih.gov/pubmed/24643083 https://www.proquest.com/docview/1531051562 https://www.proquest.com/docview/1534827504 https://pubmed.ncbi.nlm.nih.gov/PMC4050243 |
Volume | 34 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3fa9UwFD7o9qAvops_OueIKHsyrk2T_tiLbNeNITgvc4OCSEnaBCva3rm7gf_9zslt6x1TH0sPbch3mnxJTr8P4HUtKulEanmS1JrLSGue5cLy3Aib5i6MrLfz-XicHJ3JD4Uq-g23i76schgT_UBddxXtke_glxmRH0ki3s3OOblG0elqb6FxF1ZJuoyyOi3GBRexC1_CKNKI46Bc9BqbYZztfK-Mox_RI_mWuO_ynHSLaN6ul1wq-vLz0OFDeNATSLa3QPwR3LHtGqzvtbh4_vmbbTNf0un3ytfg3mSwc1uH4v1Q-EJQsM6xL1E0-TrdPxEZM43_uYXNujlVD-Hzm5ZdNVfdLtPMNcgQmTfzY6efp5-YwQmQdtiZ16Z9DGeHB6eTI97bKvBKRcmcp9iHlcFxrUJ8nKnC3LhM1VLXoaNDPERP4aUSJiI_9DpFEmIUgpbELncmiZ_AStu19hmwVIexVMbkyuYyiQ0u3mojtFAaJ71aiADeDB1bVr3mOFlf_Cj92XeclR6HknAoZRLA9hg-W4ht_Ctwc0Cp7L-5i_JPhgTwcryNvUxHILq13aWPId1TFcoAni5AHd8kJLIzzJkA0htwjwGkxH3zTtt884rcyHpJ2TGAV5QYS036W-M3_t_453CfAhflaJuwMv91aV8g8ZmbLZ_dW7C6f3A8PbkG3NECnA |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1bb9UwDLbGeBgvCDYuhQFBwJ4oa9OkFySExhnTGbswwZlUCaHStIkogvbAzob2p_iN2OmFMw1422OVNLViu7Zjxx_A45IXwvBIu2FY5q7w89yNE67dRHEdJcbztYXz2dsPx4fiTSrTBfjV34Whssr-n2h_1GVT0Bn5OmqmT3gkIX85_e4SahRlV3sIjVYsdvTpTwzZjl5sbyJ_n3C-9XoyGrsdqoBbSD-cuREuUShU6wLJM6rwEmViWYq89AzlsJB4iY-SK5_gwMsIbbCSSHMYmMSoMMB1L8FlNLweBXtROgR45M3Ykkke-S4agbTr6ekF8fqXQhm6-O6LZ-Rrz9vAc47t-frMuSIza_e2rsHVzmFlG62EXYcFXS_DykaNwfq3U7bGbAmpPZtfhqVRDx-3AulmX2hDrGeNYR98f_Tx4NU7HjNV2cs0bNrMqFoJ169qdlKdNM9ZzkyFHimz4IFs8v7gLVNocOlEn9leuDfg8EI2_CYs1k2tbwOLci8QUqlE6kSEgcJgsVQ85zJHI1ty7sDTfmOzoutxTlAbXzObaw_izPIhIz5kInRgbZg-bZt7_Gvias-lrNPxo-yPRDrwcBjGXaaUS17r5tjOoT6r0hMO3GqZOnyJC_QGUWYciM6we5hAnb_PjtTVZ9sBHL1s6iTpwCMSjDmS_kb8nf8T_wCWxpO93Wx3e3_nLlyhl9pSuFVYnP041vfQ6Zqp-1bSGXy6aNX6DVTbPgU |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Determination+of+%5B+super%2811%29C%5DPBR28+binding+potential+in+vivo%3A+a+first+human+TSPO+blocking+study&rft.jtitle=Journal+of+cerebral+blood+flow+and+metabolism&rft.au=Owen%2C+David+R&rft.au=Guo%2C+Qi&rft.au=Kalk%2C+Nicola+J&rft.au=Colasanti%2C+Alessandro&rft.date=2014-06-01&rft.issn=0271-678X&rft.volume=34&rft.issue=6&rft.spage=989&rft.epage=994&rft_id=info:doi/10.1038%2Fjcbfm.2014.46&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0271-678X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0271-678X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0271-678X&client=summon |