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...

Full description

Saved in:
Bibliographic Details
Published inJournal of cerebral blood flow and metabolism Vol. 34; no. 6; pp. 989 - 994
Main Authors Owen, David R, Guo, Qi, Kalk, Nicola J, Colasanti, Alessandro, Kalogiannopoulou, Dimitra, Dimber, Rahul, Lewis, Yvonne L, Libri, Vincenzo, Barletta, Julien, Ramada-Magalhaes, Joaquim, Kamalakaran, Aruloly, Nutt, David J, Passchier, Jan, Matthews, Paul M, Gunn, Roger N, Rabiner, Eugenii A
Format Journal Article
LanguageEnglish
Published London, England SAGE Publications 01.06.2014
Sage Publications Ltd
Nature Publishing Group
Subjects
Online AccessGet 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