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The intestinal permeability marker FITC-dextran 4kDa should be dosed according to lean body mass in obese mice
AIMS: To investigate the influence of the dose in the FITC-Dextran 4kDa (FD-4) permeability test in an obese mouse model, we tested the bodyweight dose regimen and a lean body mass-based dose regimen in high fat diet (HFD) mice and low fat diet (LFD) mice. We hypothesized that the FD-4 permeation re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816099/ https://www.ncbi.nlm.nih.gov/pubmed/36604407 http://dx.doi.org/10.1038/s41387-022-00230-2 |
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author | Voetmann, Louise M. Rolin, Bidda Kirk, Rikke K. Pyke, Charles Hansen, Axel K. |
author_facet | Voetmann, Louise M. Rolin, Bidda Kirk, Rikke K. Pyke, Charles Hansen, Axel K. |
author_sort | Voetmann, Louise M. |
collection | PubMed |
description | AIMS: To investigate the influence of the dose in the FITC-Dextran 4kDa (FD-4) permeability test in an obese mouse model, we tested the bodyweight dose regimen and a lean body mass-based dose regimen in high fat diet (HFD) mice and low fat diet (LFD) mice. We hypothesized that the FD-4 permeation result would be dose-dependent. METHODS: The two dose regimens were compared in HFD and LFD mice. Furthermore, we conducted a dose-response study to test the effect of a low or high dose of FD-4 in weight-stratified lean mice. Gene analysis of tight junctions was also carried out. RESULTS: The FD-4 intestinal permeability test was dose-dependent as we found a significant increase in plasma levels of FD-4 in obese mice with the bodyweight dose regimen. However, this difference was not detectable with the lean body mass dose regimen, even with variability-adjusted group sizes. However, the qPCR analysis revealed a decrease in tight junction gene expression in obese mice. Furthermore, we found a dose-dependent significant increase in FD-4 measured in plasma samples in lean mice. No significant difference in intestinal weight was observed between lean and obese mice. CONCLUSION: Evaluation of the intestinal permeability by FD-4 with the typical bodyweight dose regimen in obese mice will be confounded by the significant difference in dose given when compared to a lean control group. If the test dose is based on lean body mass, no significant difference in intestinal permeability is observed, even with large group sizes. Furthermore, we showed a dose-dependent difference in plasma FD-4 levels in lean mice. Therefore, we conclude that the dose should be based on lean body mass for the FD-4 permeability test if mice with considerable obesity differences are to be compared or to use another test with fixed doses. [Image: see text] |
format | Online Article Text |
id | pubmed-9816099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98160992023-01-07 The intestinal permeability marker FITC-dextran 4kDa should be dosed according to lean body mass in obese mice Voetmann, Louise M. Rolin, Bidda Kirk, Rikke K. Pyke, Charles Hansen, Axel K. Nutr Diabetes Technical Report AIMS: To investigate the influence of the dose in the FITC-Dextran 4kDa (FD-4) permeability test in an obese mouse model, we tested the bodyweight dose regimen and a lean body mass-based dose regimen in high fat diet (HFD) mice and low fat diet (LFD) mice. We hypothesized that the FD-4 permeation result would be dose-dependent. METHODS: The two dose regimens were compared in HFD and LFD mice. Furthermore, we conducted a dose-response study to test the effect of a low or high dose of FD-4 in weight-stratified lean mice. Gene analysis of tight junctions was also carried out. RESULTS: The FD-4 intestinal permeability test was dose-dependent as we found a significant increase in plasma levels of FD-4 in obese mice with the bodyweight dose regimen. However, this difference was not detectable with the lean body mass dose regimen, even with variability-adjusted group sizes. However, the qPCR analysis revealed a decrease in tight junction gene expression in obese mice. Furthermore, we found a dose-dependent significant increase in FD-4 measured in plasma samples in lean mice. No significant difference in intestinal weight was observed between lean and obese mice. CONCLUSION: Evaluation of the intestinal permeability by FD-4 with the typical bodyweight dose regimen in obese mice will be confounded by the significant difference in dose given when compared to a lean control group. If the test dose is based on lean body mass, no significant difference in intestinal permeability is observed, even with large group sizes. Furthermore, we showed a dose-dependent difference in plasma FD-4 levels in lean mice. Therefore, we conclude that the dose should be based on lean body mass for the FD-4 permeability test if mice with considerable obesity differences are to be compared or to use another test with fixed doses. [Image: see text] Nature Publishing Group UK 2023-01-05 /pmc/articles/PMC9816099/ /pubmed/36604407 http://dx.doi.org/10.1038/s41387-022-00230-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Technical Report Voetmann, Louise M. Rolin, Bidda Kirk, Rikke K. Pyke, Charles Hansen, Axel K. The intestinal permeability marker FITC-dextran 4kDa should be dosed according to lean body mass in obese mice |
title | The intestinal permeability marker FITC-dextran 4kDa should be dosed according to lean body mass in obese mice |
title_full | The intestinal permeability marker FITC-dextran 4kDa should be dosed according to lean body mass in obese mice |
title_fullStr | The intestinal permeability marker FITC-dextran 4kDa should be dosed according to lean body mass in obese mice |
title_full_unstemmed | The intestinal permeability marker FITC-dextran 4kDa should be dosed according to lean body mass in obese mice |
title_short | The intestinal permeability marker FITC-dextran 4kDa should be dosed according to lean body mass in obese mice |
title_sort | intestinal permeability marker fitc-dextran 4kda should be dosed according to lean body mass in obese mice |
topic | Technical Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816099/ https://www.ncbi.nlm.nih.gov/pubmed/36604407 http://dx.doi.org/10.1038/s41387-022-00230-2 |
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