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Assessment of brain beta-amyloid deposition in transgenic mouse models of Alzheimer’s disease with PET imaging agents (18)F-flutemetamol and (18)F-florbetaben

BACKGROUND: Although amyloid beta (Aβ) imaging is widely used for diagnosing and monitoring Alzheimer’s disease in clinical fields, paralleling comparison between (18)F-flutemetamol and (18)F-florbetaben was rarely attempted in AD mouse model. We performed a comparison of Aβ PET images between (18)F...

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Autores principales: Son, Hye Joo, Jeong, Young Jin, Yoon, Hyun Jin, Lee, Sang Yoon, Choi, Go-Eun, Park, Ji-Ae, Kim, Min Hwan, Lee, Kyo Chul, Lee, Yong Jin, Kim, Mun Ki, Cho, Kook, Kang, Do-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063010/
https://www.ncbi.nlm.nih.gov/pubmed/30053803
http://dx.doi.org/10.1186/s12868-018-0447-7
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author Son, Hye Joo
Jeong, Young Jin
Yoon, Hyun Jin
Lee, Sang Yoon
Choi, Go-Eun
Park, Ji-Ae
Kim, Min Hwan
Lee, Kyo Chul
Lee, Yong Jin
Kim, Mun Ki
Cho, Kook
Kang, Do-Young
author_facet Son, Hye Joo
Jeong, Young Jin
Yoon, Hyun Jin
Lee, Sang Yoon
Choi, Go-Eun
Park, Ji-Ae
Kim, Min Hwan
Lee, Kyo Chul
Lee, Yong Jin
Kim, Mun Ki
Cho, Kook
Kang, Do-Young
author_sort Son, Hye Joo
collection PubMed
description BACKGROUND: Although amyloid beta (Aβ) imaging is widely used for diagnosing and monitoring Alzheimer’s disease in clinical fields, paralleling comparison between (18)F-flutemetamol and (18)F-florbetaben was rarely attempted in AD mouse model. We performed a comparison of Aβ PET images between (18)F-flutemetamol and (18)F-florbetaben in a recently developed APPswe mouse model, C57BL/6-Tg (NSE-hAPPsw) Korl. RESULTS: After an injection (0.23 mCi) of (18)F-flutemetamol and (18)F-florbetaben at a time interval of 2–3 days, we compared group difference of SUVR and kinetic parameters between the AD (n = 7) and control (n = 7) mice, as well as between (18)F-flutemetamol and (18)F-florbetaben image. In addition, bio-distribution and histopathology were conducted. With visual image and VOI-based SUVR analysis, the AD group presented more prominent uptake than did the control group in both the (18)F-florbetaben and (18)F-flutemetamol images. With kinetic analysis, the (18)F-florbetaben images showed differences in K1 and k4 between the AD and control groups, although (18)F-flutemetamol images did not show significant difference. (18)F-florbetaben images showed more prominent cortical uptake and matched well to the thioflavin S staining images than did the (18)F-flutemetamol image. In contrast, (18)F-flutemetamol images presented higher K1, k4, K1/k2 values than those of (18)F-florbetaben images. Also, (18)F-flutemetamol images presented prominent uptake in the bowel and bladder, consistent with higher bio-distribution in kidney, lung, blood and heart. CONCLUSIONS: Compared with (18)F-flutemetamol images, (18)F-florbetaben images showed prominent visual uptake intensity, SUVR, and higher correlations with the pathology. In contrast, (18)F-flutemetamol was more actively metabolized than was (18)F-florbetaben (Son et al. in J Nucl Med 58(Suppl 1):S278, 2017]. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12868-018-0447-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-60630102018-07-31 Assessment of brain beta-amyloid deposition in transgenic mouse models of Alzheimer’s disease with PET imaging agents (18)F-flutemetamol and (18)F-florbetaben Son, Hye Joo Jeong, Young Jin Yoon, Hyun Jin Lee, Sang Yoon Choi, Go-Eun Park, Ji-Ae Kim, Min Hwan Lee, Kyo Chul Lee, Yong Jin Kim, Mun Ki Cho, Kook Kang, Do-Young BMC Neurosci Research Article BACKGROUND: Although amyloid beta (Aβ) imaging is widely used for diagnosing and monitoring Alzheimer’s disease in clinical fields, paralleling comparison between (18)F-flutemetamol and (18)F-florbetaben was rarely attempted in AD mouse model. We performed a comparison of Aβ PET images between (18)F-flutemetamol and (18)F-florbetaben in a recently developed APPswe mouse model, C57BL/6-Tg (NSE-hAPPsw) Korl. RESULTS: After an injection (0.23 mCi) of (18)F-flutemetamol and (18)F-florbetaben at a time interval of 2–3 days, we compared group difference of SUVR and kinetic parameters between the AD (n = 7) and control (n = 7) mice, as well as between (18)F-flutemetamol and (18)F-florbetaben image. In addition, bio-distribution and histopathology were conducted. With visual image and VOI-based SUVR analysis, the AD group presented more prominent uptake than did the control group in both the (18)F-florbetaben and (18)F-flutemetamol images. With kinetic analysis, the (18)F-florbetaben images showed differences in K1 and k4 between the AD and control groups, although (18)F-flutemetamol images did not show significant difference. (18)F-florbetaben images showed more prominent cortical uptake and matched well to the thioflavin S staining images than did the (18)F-flutemetamol image. In contrast, (18)F-flutemetamol images presented higher K1, k4, K1/k2 values than those of (18)F-florbetaben images. Also, (18)F-flutemetamol images presented prominent uptake in the bowel and bladder, consistent with higher bio-distribution in kidney, lung, blood and heart. CONCLUSIONS: Compared with (18)F-flutemetamol images, (18)F-florbetaben images showed prominent visual uptake intensity, SUVR, and higher correlations with the pathology. In contrast, (18)F-flutemetamol was more actively metabolized than was (18)F-florbetaben (Son et al. in J Nucl Med 58(Suppl 1):S278, 2017]. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12868-018-0447-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-27 /pmc/articles/PMC6063010/ /pubmed/30053803 http://dx.doi.org/10.1186/s12868-018-0447-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Son, Hye Joo
Jeong, Young Jin
Yoon, Hyun Jin
Lee, Sang Yoon
Choi, Go-Eun
Park, Ji-Ae
Kim, Min Hwan
Lee, Kyo Chul
Lee, Yong Jin
Kim, Mun Ki
Cho, Kook
Kang, Do-Young
Assessment of brain beta-amyloid deposition in transgenic mouse models of Alzheimer’s disease with PET imaging agents (18)F-flutemetamol and (18)F-florbetaben
title Assessment of brain beta-amyloid deposition in transgenic mouse models of Alzheimer’s disease with PET imaging agents (18)F-flutemetamol and (18)F-florbetaben
title_full Assessment of brain beta-amyloid deposition in transgenic mouse models of Alzheimer’s disease with PET imaging agents (18)F-flutemetamol and (18)F-florbetaben
title_fullStr Assessment of brain beta-amyloid deposition in transgenic mouse models of Alzheimer’s disease with PET imaging agents (18)F-flutemetamol and (18)F-florbetaben
title_full_unstemmed Assessment of brain beta-amyloid deposition in transgenic mouse models of Alzheimer’s disease with PET imaging agents (18)F-flutemetamol and (18)F-florbetaben
title_short Assessment of brain beta-amyloid deposition in transgenic mouse models of Alzheimer’s disease with PET imaging agents (18)F-flutemetamol and (18)F-florbetaben
title_sort assessment of brain beta-amyloid deposition in transgenic mouse models of alzheimer’s disease with pet imaging agents (18)f-flutemetamol and (18)f-florbetaben
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063010/
https://www.ncbi.nlm.nih.gov/pubmed/30053803
http://dx.doi.org/10.1186/s12868-018-0447-7
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