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Assessment of TSPO in a Rat Experimental Autoimmune Myocarditis Model: A Comparison Study between [(18)F]Fluoromethyl-PBR28 and [(18)F]CB251

Overexpression of the 18-kDa translocator protein (TSPO) is closely linked to inflammatory responses in the heart, including myocarditis, which can lead to myocardial necrosis. In vivo assessment of inflammatory responses has enabled the precise diagnosis of myocarditis to improve clinical outcomes....

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Autores principales: Kim, Ga Ram, Paeng, Jin Chul, Jung, Jae Ho, Moon, Byung Seok, Lopalco, Antonio, Denora, Nunzio, Lee, Byung Chul, Kim, Sang Eun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796222/
https://www.ncbi.nlm.nih.gov/pubmed/29342117
http://dx.doi.org/10.3390/ijms19010276
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author Kim, Ga Ram
Paeng, Jin Chul
Jung, Jae Ho
Moon, Byung Seok
Lopalco, Antonio
Denora, Nunzio
Lee, Byung Chul
Kim, Sang Eun
author_facet Kim, Ga Ram
Paeng, Jin Chul
Jung, Jae Ho
Moon, Byung Seok
Lopalco, Antonio
Denora, Nunzio
Lee, Byung Chul
Kim, Sang Eun
author_sort Kim, Ga Ram
collection PubMed
description Overexpression of the 18-kDa translocator protein (TSPO) is closely linked to inflammatory responses in the heart, including myocarditis, which can lead to myocardial necrosis. In vivo assessment of inflammatory responses has enabled the precise diagnosis of myocarditis to improve clinical outcomes. Here, we evaluated TSPO overexpression in a rat model of experimental autoimmune myocarditis (EAM) compared to healthy rats using two TSPO radiotracers, [(18)F]fluoromethyl-PBR28 ([(18)F]1) and [(18)F]CB251 ([(18)F]2). All radiolabeling methods were successfully applied to an automated module for the reproducible preparation of TSPO radiotracers. Both radiotracers were directly compared in an EAM rat model, as well as in healthy rats to determine whether either radiotracer provides a more promising assessment of in vivo TSPO overexpression. [(18)F]2 provided more specific TSPO-uptake in the heart of the EAM rats (1.32-fold that of the heart-to-lung uptake ratio versus healthy controls), while [(18)F]1 did not show a significant difference between the two groups. Histopathological characterization revealed that a prominent positron emission tomography (PET) signal of [(18)F]2 in the EAM rats corresponded to the presence of a higher density of TSPO compared to the healthy controls. These results suggest that the imidazole[1,2-a]pyridine-based radiotracer [(18)F]2 is a sensitive tool for noninvasively diagnosing myocarditis related to inflammation of the heart muscle by assessing abnormal TSPO expression.
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spelling pubmed-57962222018-02-09 Assessment of TSPO in a Rat Experimental Autoimmune Myocarditis Model: A Comparison Study between [(18)F]Fluoromethyl-PBR28 and [(18)F]CB251 Kim, Ga Ram Paeng, Jin Chul Jung, Jae Ho Moon, Byung Seok Lopalco, Antonio Denora, Nunzio Lee, Byung Chul Kim, Sang Eun Int J Mol Sci Article Overexpression of the 18-kDa translocator protein (TSPO) is closely linked to inflammatory responses in the heart, including myocarditis, which can lead to myocardial necrosis. In vivo assessment of inflammatory responses has enabled the precise diagnosis of myocarditis to improve clinical outcomes. Here, we evaluated TSPO overexpression in a rat model of experimental autoimmune myocarditis (EAM) compared to healthy rats using two TSPO radiotracers, [(18)F]fluoromethyl-PBR28 ([(18)F]1) and [(18)F]CB251 ([(18)F]2). All radiolabeling methods were successfully applied to an automated module for the reproducible preparation of TSPO radiotracers. Both radiotracers were directly compared in an EAM rat model, as well as in healthy rats to determine whether either radiotracer provides a more promising assessment of in vivo TSPO overexpression. [(18)F]2 provided more specific TSPO-uptake in the heart of the EAM rats (1.32-fold that of the heart-to-lung uptake ratio versus healthy controls), while [(18)F]1 did not show a significant difference between the two groups. Histopathological characterization revealed that a prominent positron emission tomography (PET) signal of [(18)F]2 in the EAM rats corresponded to the presence of a higher density of TSPO compared to the healthy controls. These results suggest that the imidazole[1,2-a]pyridine-based radiotracer [(18)F]2 is a sensitive tool for noninvasively diagnosing myocarditis related to inflammation of the heart muscle by assessing abnormal TSPO expression. MDPI 2018-01-17 /pmc/articles/PMC5796222/ /pubmed/29342117 http://dx.doi.org/10.3390/ijms19010276 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Ga Ram
Paeng, Jin Chul
Jung, Jae Ho
Moon, Byung Seok
Lopalco, Antonio
Denora, Nunzio
Lee, Byung Chul
Kim, Sang Eun
Assessment of TSPO in a Rat Experimental Autoimmune Myocarditis Model: A Comparison Study between [(18)F]Fluoromethyl-PBR28 and [(18)F]CB251
title Assessment of TSPO in a Rat Experimental Autoimmune Myocarditis Model: A Comparison Study between [(18)F]Fluoromethyl-PBR28 and [(18)F]CB251
title_full Assessment of TSPO in a Rat Experimental Autoimmune Myocarditis Model: A Comparison Study between [(18)F]Fluoromethyl-PBR28 and [(18)F]CB251
title_fullStr Assessment of TSPO in a Rat Experimental Autoimmune Myocarditis Model: A Comparison Study between [(18)F]Fluoromethyl-PBR28 and [(18)F]CB251
title_full_unstemmed Assessment of TSPO in a Rat Experimental Autoimmune Myocarditis Model: A Comparison Study between [(18)F]Fluoromethyl-PBR28 and [(18)F]CB251
title_short Assessment of TSPO in a Rat Experimental Autoimmune Myocarditis Model: A Comparison Study between [(18)F]Fluoromethyl-PBR28 and [(18)F]CB251
title_sort assessment of tspo in a rat experimental autoimmune myocarditis model: a comparison study between [(18)f]fluoromethyl-pbr28 and [(18)f]cb251
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796222/
https://www.ncbi.nlm.nih.gov/pubmed/29342117
http://dx.doi.org/10.3390/ijms19010276
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