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Permeability of the Cyanotoxin Microcystin-RR across a Caco-2 Cells Monolayer
Microcystins (MCs) are toxins produced by several cyanobacterial species found worldwide. While MCs have a common structure, the variation of two amino acids in their structure affects their toxicity. As toxicodynamics are very similar between the MC variants, their differential toxicity could rathe...
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/PMC7997155/ https://www.ncbi.nlm.nih.gov/pubmed/33673481 http://dx.doi.org/10.3390/toxins13030178 |
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author | Henri, Jérôme Lanceleur, Rachelle Delmas, Jean-Michel Fessard, Valérie Huguet, Antoine |
author_facet | Henri, Jérôme Lanceleur, Rachelle Delmas, Jean-Michel Fessard, Valérie Huguet, Antoine |
author_sort | Henri, Jérôme |
collection | PubMed |
description | Microcystins (MCs) are toxins produced by several cyanobacterial species found worldwide. While MCs have a common structure, the variation of two amino acids in their structure affects their toxicity. As toxicodynamics are very similar between the MC variants, their differential toxicity could rather be explained by toxicokinetic parameters. Microcystin-RR (MC-RR) is the second most abundant congener and induces toxicity through oral exposure. As intestinal permeability is a key parameter of oral toxicokinetics, the apparent permeability of MC-RR across a differentiated intestinal Caco-2 cell monolayer was investigated. We observed a rapid and large decrease of MC-RR levels in the donor compartment. However, irrespective of the loaded concentration and exposure time, the permeabilities were very low from apical to basolateral compartments (from 4 to 15 × 10(−8) cm·s(−1)) and from basolateral to apical compartments (from 2 to 37 × 10(−8) cm·s(−1)). Our results suggested that MC-RR would be poorly absorbed orally. As similar low permeability was reported for the most abundant congener microcystin-LR, and this variant presented a greater acute oral toxicity than MC-RR, we concluded that the intestinal permeability was probably not involved in the differential toxicity between them, in contrast to the hepatic uptake and metabolism. |
format | Online Article Text |
id | pubmed-7997155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79971552021-03-27 Permeability of the Cyanotoxin Microcystin-RR across a Caco-2 Cells Monolayer Henri, Jérôme Lanceleur, Rachelle Delmas, Jean-Michel Fessard, Valérie Huguet, Antoine Toxins (Basel) Article Microcystins (MCs) are toxins produced by several cyanobacterial species found worldwide. While MCs have a common structure, the variation of two amino acids in their structure affects their toxicity. As toxicodynamics are very similar between the MC variants, their differential toxicity could rather be explained by toxicokinetic parameters. Microcystin-RR (MC-RR) is the second most abundant congener and induces toxicity through oral exposure. As intestinal permeability is a key parameter of oral toxicokinetics, the apparent permeability of MC-RR across a differentiated intestinal Caco-2 cell monolayer was investigated. We observed a rapid and large decrease of MC-RR levels in the donor compartment. However, irrespective of the loaded concentration and exposure time, the permeabilities were very low from apical to basolateral compartments (from 4 to 15 × 10(−8) cm·s(−1)) and from basolateral to apical compartments (from 2 to 37 × 10(−8) cm·s(−1)). Our results suggested that MC-RR would be poorly absorbed orally. As similar low permeability was reported for the most abundant congener microcystin-LR, and this variant presented a greater acute oral toxicity than MC-RR, we concluded that the intestinal permeability was probably not involved in the differential toxicity between them, in contrast to the hepatic uptake and metabolism. MDPI 2021-02-27 /pmc/articles/PMC7997155/ /pubmed/33673481 http://dx.doi.org/10.3390/toxins13030178 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 (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Henri, Jérôme Lanceleur, Rachelle Delmas, Jean-Michel Fessard, Valérie Huguet, Antoine Permeability of the Cyanotoxin Microcystin-RR across a Caco-2 Cells Monolayer |
title | Permeability of the Cyanotoxin Microcystin-RR across a Caco-2 Cells Monolayer |
title_full | Permeability of the Cyanotoxin Microcystin-RR across a Caco-2 Cells Monolayer |
title_fullStr | Permeability of the Cyanotoxin Microcystin-RR across a Caco-2 Cells Monolayer |
title_full_unstemmed | Permeability of the Cyanotoxin Microcystin-RR across a Caco-2 Cells Monolayer |
title_short | Permeability of the Cyanotoxin Microcystin-RR across a Caco-2 Cells Monolayer |
title_sort | permeability of the cyanotoxin microcystin-rr across a caco-2 cells monolayer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997155/ https://www.ncbi.nlm.nih.gov/pubmed/33673481 http://dx.doi.org/10.3390/toxins13030178 |
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