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[(18)F]Fluorothymidine Uptake in the Porcine Pancreatic Elastase-Induced Model of Abdominal Aortic Aneurysm
The porcine pancreatic elastase (PPE) model is a common preclinical model of abdominal aortic aneurysms (AAA). Some notable characteristics of this model include the low aortic rupture rate, non-progressive disease course, and infra-renal AAA formation. Enhanced [(18)F]fluorothymidine ([(18)F]FLT) u...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404933/ https://www.ncbi.nlm.nih.gov/pubmed/34460766 http://dx.doi.org/10.3390/jimaging7080130 |
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author | Gandhi, Richa Koch-Paszkowski, Joanna Tsoumpas, Charalampos Bailey, Marc A. |
author_facet | Gandhi, Richa Koch-Paszkowski, Joanna Tsoumpas, Charalampos Bailey, Marc A. |
author_sort | Gandhi, Richa |
collection | PubMed |
description | The porcine pancreatic elastase (PPE) model is a common preclinical model of abdominal aortic aneurysms (AAA). Some notable characteristics of this model include the low aortic rupture rate, non-progressive disease course, and infra-renal AAA formation. Enhanced [(18)F]fluorothymidine ([(18)F]FLT) uptake on positron emission tomography/computed tomography (PET/CT) has previously been reported in the angiotensin II-induced murine model of AAA. Here, we report our preliminary findings of investigating [(18)F]FLT uptake in the PPE murine model of AAA. [(18)F]FLT uptake was found to be substantially increased in the abdominal areas recovering from the surgery, whilst it was not found to be significantly increased within the PPE-induced AAA, as confirmed using in vivo PET/CT and ex vivo whole-organ gamma counting (PPE, n = 7; controls, n = 3). This finding suggests that the [(18)F]FLT may not be an appropriate radiotracer for this specific AAA model, and further studies with larger sample sizes are warranted to elucidate the pathobiology contributing to the reduced uptake of [(18)F]FLT in this model. |
format | Online Article Text |
id | pubmed-8404933 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84049332021-10-28 [(18)F]Fluorothymidine Uptake in the Porcine Pancreatic Elastase-Induced Model of Abdominal Aortic Aneurysm Gandhi, Richa Koch-Paszkowski, Joanna Tsoumpas, Charalampos Bailey, Marc A. J Imaging Brief Report The porcine pancreatic elastase (PPE) model is a common preclinical model of abdominal aortic aneurysms (AAA). Some notable characteristics of this model include the low aortic rupture rate, non-progressive disease course, and infra-renal AAA formation. Enhanced [(18)F]fluorothymidine ([(18)F]FLT) uptake on positron emission tomography/computed tomography (PET/CT) has previously been reported in the angiotensin II-induced murine model of AAA. Here, we report our preliminary findings of investigating [(18)F]FLT uptake in the PPE murine model of AAA. [(18)F]FLT uptake was found to be substantially increased in the abdominal areas recovering from the surgery, whilst it was not found to be significantly increased within the PPE-induced AAA, as confirmed using in vivo PET/CT and ex vivo whole-organ gamma counting (PPE, n = 7; controls, n = 3). This finding suggests that the [(18)F]FLT may not be an appropriate radiotracer for this specific AAA model, and further studies with larger sample sizes are warranted to elucidate the pathobiology contributing to the reduced uptake of [(18)F]FLT in this model. MDPI 2021-08-04 /pmc/articles/PMC8404933/ /pubmed/34460766 http://dx.doi.org/10.3390/jimaging7080130 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Brief Report Gandhi, Richa Koch-Paszkowski, Joanna Tsoumpas, Charalampos Bailey, Marc A. [(18)F]Fluorothymidine Uptake in the Porcine Pancreatic Elastase-Induced Model of Abdominal Aortic Aneurysm |
title | [(18)F]Fluorothymidine Uptake in the Porcine Pancreatic Elastase-Induced Model of Abdominal Aortic Aneurysm |
title_full | [(18)F]Fluorothymidine Uptake in the Porcine Pancreatic Elastase-Induced Model of Abdominal Aortic Aneurysm |
title_fullStr | [(18)F]Fluorothymidine Uptake in the Porcine Pancreatic Elastase-Induced Model of Abdominal Aortic Aneurysm |
title_full_unstemmed | [(18)F]Fluorothymidine Uptake in the Porcine Pancreatic Elastase-Induced Model of Abdominal Aortic Aneurysm |
title_short | [(18)F]Fluorothymidine Uptake in the Porcine Pancreatic Elastase-Induced Model of Abdominal Aortic Aneurysm |
title_sort | [(18)f]fluorothymidine uptake in the porcine pancreatic elastase-induced model of abdominal aortic aneurysm |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404933/ https://www.ncbi.nlm.nih.gov/pubmed/34460766 http://dx.doi.org/10.3390/jimaging7080130 |
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