Skip to main content
Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging 12/2016

19.07.2016 | Original Article

Characterization of the radiolabeled metabolite of tau PET tracer 18F-THK5351

verfasst von: Ryuichi Harada, Shozo Furumoto, Tetsuro Tago, Furukawa Katsutoshi, Aiko Ishiki, Naoki Tomita, Ren Iwata, Manabu Tashiro, Hiroyuki Arai, Kazuhiko Yanai, Yukitsuka Kudo, Nobuyuki Okamura

Erschienen in: European Journal of Nuclear Medicine and Molecular Imaging | Ausgabe 12/2016

Einloggen, um Zugang zu erhalten

Abstract

Purpose

18F-THK5351 is a novel radiotracer developed for in vivo imaging of tau pathology in the brain. For the quantitative assessment of tau deposits in the brain, it is important that the radioactive metabolite does not enter the brain and that it does not bind to tau fibrils. The purpose of the study was to identify a radiolabeled metabolite of 18F-THK5351 in blood samples from human subjects and to characterize its pharmacological properties.

Methods

Venous blood samples were collected from three human subjects after injection of 18F-THK5351 and the plasma metabolite was measured by high performance thin layer chromatography. In addition, mass spectrometry analysis and enzymatic assays were used to identify this metabolite. Mice were used to investigate the blood–brain barrier permeability of the radioactive metabolite. Furthermore, the binding ability of the metabolite to tau aggregates was evaluated using autoradiography and binding assays using human brain samples.

Results

About 13 % of the unmetabolized radiotracer was detectable in human plasma at 60 min following the injection of 18F-THK5351. The isolated radiometabolite of 18F-THK5351 was the sulphoconjugate of THK5351. This metabolite could be produced in vitro by incubating THK5351 with liver but not brain homogenates. The metabolite did not penetrate the blood–brain barrier in mice, and exhibited little binding to tau protein aggregates in post-mortem human brain samples.

Conclusions

These results suggest that the sole metabolite detectable in plasma seems to be generated outside the brain and does not cross into the brain, which does not affect quantitative analysis of PET images.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
3.
Zurück zum Zitat Braak H, Braak E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol. 1991;82:239–59.CrossRefPubMed Braak H, Braak E. Neuropathological stageing of Alzheimer-related changes. Acta Neuropathol. 1991;82:239–59.CrossRefPubMed
4.
Zurück zum Zitat Delacourte A, David JP, Sergeant N, Buee L, Wattez A, Vermersch P, et al. The biochemical pathway of neurofibrillary degeneration in aging and Alzheimer’s disease. Neurology. 1999;52:1158–65.CrossRefPubMed Delacourte A, David JP, Sergeant N, Buee L, Wattez A, Vermersch P, et al. The biochemical pathway of neurofibrillary degeneration in aging and Alzheimer’s disease. Neurology. 1999;52:1158–65.CrossRefPubMed
6.
Zurück zum Zitat Villemagne VL, Furumoto S, Fodero-Tavoletti MT, Harada R, Mulligan RS, Kudo Y, et al. The challenges of Tau imaging. Future Neurol. 2012;7:409–21.CrossRef Villemagne VL, Furumoto S, Fodero-Tavoletti MT, Harada R, Mulligan RS, Kudo Y, et al. The challenges of Tau imaging. Future Neurol. 2012;7:409–21.CrossRef
9.
Zurück zum Zitat Chien DT, Bahri S, Szardenings AK, Walsh JC, Mu F, Su MY, et al. Early clinical PET imaging results with the novel PHF-tau radioligand [F-18]-T807. J Alzheimers Dis. 2013;34:457–68. doi:10.3233/JAD-122059.PubMed Chien DT, Bahri S, Szardenings AK, Walsh JC, Mu F, Su MY, et al. Early clinical PET imaging results with the novel PHF-tau radioligand [F-18]-T807. J Alzheimers Dis. 2013;34:457–68. doi:10.​3233/​JAD-122059.PubMed
10.
Zurück zum Zitat Chien DT, Szardenings AK, Bahri S, Walsh JC, Mu F, Xia C, et al. Early clinical PET imaging results with the novel PHF-tau radioligand [F18]-T808. J Alzheimers Dis. 2014;38:171–84. doi:10.3233/JAD-130098.PubMed Chien DT, Szardenings AK, Bahri S, Walsh JC, Mu F, Xia C, et al. Early clinical PET imaging results with the novel PHF-tau radioligand [F18]-T808. J Alzheimers Dis. 2014;38:171–84. doi:10.​3233/​JAD-130098.PubMed
13.
Zurück zum Zitat Tago T, Furumoto S, Okamura N, Harada R, Adachi H, Ishikawa Y, et al. Structure-activity relationship of 2-arylquinolines as PET imaging tracers for Tau pathology in Alzheimer’s disease. J Nucl Med. 2016;57:608–14. doi:10.2967/jnumed.115.166652.CrossRefPubMed Tago T, Furumoto S, Okamura N, Harada R, Adachi H, Ishikawa Y, et al. Structure-activity relationship of 2-arylquinolines as PET imaging tracers for Tau pathology in Alzheimer’s disease. J Nucl Med. 2016;57:608–14. doi:10.​2967/​jnumed.​115.​166652.CrossRefPubMed
15.
Zurück zum Zitat Harada R, Okamura N, Furumoto S, Furukawa K, Ishiki A, Tomita N, et al. [18F]THK-5117 PET for assessing neurofibrillary pathology in Alzheimer’s disease. Eur J Nucl Med Mol Imaging. 2015;42:1052–61. doi:10.1007/s00259-015-3035-4.CrossRefPubMed Harada R, Okamura N, Furumoto S, Furukawa K, Ishiki A, Tomita N, et al. [18F]THK-5117 PET for assessing neurofibrillary pathology in Alzheimer’s disease. Eur J Nucl Med Mol Imaging. 2015;42:1052–61. doi:10.​1007/​s00259-015-3035-4.CrossRefPubMed
16.
Zurück zum Zitat Okamura N, Furumoto S, Harada R, Tago T, Yoshikawa T, Fodero-Tavoletti M, et al. Novel 18F-labeled arylquinoline derivatives for noninvasive imaging of tau pathology in Alzheimer disease. J Nucl Med. 2013;54:1420–7. doi:10.2967/jnumed.112.117341.CrossRefPubMed Okamura N, Furumoto S, Harada R, Tago T, Yoshikawa T, Fodero-Tavoletti M, et al. Novel 18F-labeled arylquinoline derivatives for noninvasive imaging of tau pathology in Alzheimer disease. J Nucl Med. 2013;54:1420–7. doi:10.​2967/​jnumed.​112.​117341.CrossRefPubMed
17.
Zurück zum Zitat Sepe V, Ummarino R, D’Auria MV, Renga B, Fiorucci S, Zampella A. The first total synthesis of solomonsterol B, a marine pregnane X receptor agonist. Eur J Org Chem. 2012;2012:5187–94. doi:10.1002/ejoc.201200619.CrossRef Sepe V, Ummarino R, D’Auria MV, Renga B, Fiorucci S, Zampella A. The first total synthesis of solomonsterol B, a marine pregnane X receptor agonist. Eur J Org Chem. 2012;2012:5187–94. doi:10.​1002/​ejoc.​201200619.CrossRef
19.
Zurück zum Zitat Villemagne VL, Fodero-Tavoletti MT, Masters CL, Rowe CC. Tau imaging: early progress and future directions. Lancet Neurol. 2015;14:114–24.CrossRefPubMed Villemagne VL, Fodero-Tavoletti MT, Masters CL, Rowe CC. Tau imaging: early progress and future directions. Lancet Neurol. 2015;14:114–24.CrossRefPubMed
20.
Zurück zum Zitat Zhang W, Arteaga J, Cashion DK, Chen G, Gangadharmath U, Gomez LF, et al. A highly selective and specific PET tracer for imaging of tau pathologies. J Alzheimers Dis. 2012;31:601–12. doi:10.3233/JAD-2012-120712.PubMed Zhang W, Arteaga J, Cashion DK, Chen G, Gangadharmath U, Gomez LF, et al. A highly selective and specific PET tracer for imaging of tau pathologies. J Alzheimers Dis. 2012;31:601–12. doi:10.​3233/​JAD-2012-120712.PubMed
22.
Zurück zum Zitat Hashimoto H, Kawamura K, Igarashi N, Takei M, Fujishiro T, Aihara Y, et al. Radiosynthesis, photoisomerization, biodistribution, and metabolite analysis of 11C-PBB3 as a clinically useful PET probe for imaging of tau pathology. J Nucl Med. 2014;55:1532–8. doi:10.2967/jnumed.114.139550.CrossRefPubMed Hashimoto H, Kawamura K, Igarashi N, Takei M, Fujishiro T, Aihara Y, et al. Radiosynthesis, photoisomerization, biodistribution, and metabolite analysis of 11C-PBB3 as a clinically useful PET probe for imaging of tau pathology. J Nucl Med. 2014;55:1532–8. doi:10.​2967/​jnumed.​114.​139550.CrossRefPubMed
26.
Zurück zum Zitat Normandin M, Collier T, Wooten D, Kolnick A, Yokell D, Shoup T, et al. Pharmacokinetic evaluation of the tau radiotracer [F-18]T807 and cerebral binding in a subject with traumatic brain injury. J Nucl Med. 2014;55. Normandin M, Collier T, Wooten D, Kolnick A, Yokell D, Shoup T, et al. Pharmacokinetic evaluation of the tau radiotracer [F-18]T807 and cerebral binding in a subject with traumatic brain injury. J Nucl Med. 2014;55.
27.
Zurück zum Zitat Jonasson M, Wall A, Chiotis K, Saint-Aubert L, Wilking H, Sprycha M, et al. Tracer kinetic analysis of (S)-18F-THK5117 as a PET tracer for assessing tau pathology. J Nucl Med. 2016. doi:10.2967/jnumed.115.158519.PubMed Jonasson M, Wall A, Chiotis K, Saint-Aubert L, Wilking H, Sprycha M, et al. Tracer kinetic analysis of (S)-18F-THK5117 as a PET tracer for assessing tau pathology. J Nucl Med. 2016. doi:10.​2967/​jnumed.​115.​158519.PubMed
28.
30.
31.
Zurück zum Zitat Falany CN, Krasnykh V, Falany JL. Bacterial expression and characterization of a cDNA for human liver estrogen sulfotransferase. J Steroid Biochem Mol Biol. 1995;52:529–39.CrossRefPubMed Falany CN, Krasnykh V, Falany JL. Bacterial expression and characterization of a cDNA for human liver estrogen sulfotransferase. J Steroid Biochem Mol Biol. 1995;52:529–39.CrossRefPubMed
32.
Zurück zum Zitat Mathis CA, Holt D, Wang YM, Huang GF, Debnath M, Shao L, et al. Species-dependent formation and identification of the brain metabolites of the amyloid imaging agent [C-11]PIB. Neurobiol Aging. 2004;25:S277–S8. doi:10.1016/S0197-4580(04)80924-2.CrossRef Mathis CA, Holt D, Wang YM, Huang GF, Debnath M, Shao L, et al. Species-dependent formation and identification of the brain metabolites of the amyloid imaging agent [C-11]PIB. Neurobiol Aging. 2004;25:S277–S8. doi:10.​1016/​S0197-4580(04)80924-2.CrossRef
Metadaten
Titel
Characterization of the radiolabeled metabolite of tau PET tracer 18F-THK5351
verfasst von
Ryuichi Harada
Shozo Furumoto
Tetsuro Tago
Furukawa Katsutoshi
Aiko Ishiki
Naoki Tomita
Ren Iwata
Manabu Tashiro
Hiroyuki Arai
Kazuhiko Yanai
Yukitsuka Kudo
Nobuyuki Okamura
Publikationsdatum
19.07.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
European Journal of Nuclear Medicine and Molecular Imaging / Ausgabe 12/2016
Print ISSN: 1619-7070
Elektronische ISSN: 1619-7089
DOI
https://doi.org/10.1007/s00259-016-3453-y

Weitere Artikel der Ausgabe 12/2016

European Journal of Nuclear Medicine and Molecular Imaging 12/2016 Zur Ausgabe