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Spatiotemporal role of muscarinic signaling in early chick development: exposure to cholinomimetic agents by a mathematical model

Awareness is growing that, besides several neurotoxic effects, cholinomimetic drugs able to interfere the cholinergic neurotransmitter system may exert a teratogen effect in developing embryos of vertebrate and invertebrate organisms. Cholinomimetic substances exert their toxic activity on organisms...

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Autores principales: Paladino, Ombretta, Moranda, Arianna, Falugi, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425487/
https://www.ncbi.nlm.nih.gov/pubmed/36098822
http://dx.doi.org/10.1007/s10565-022-09770-w
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author Paladino, Ombretta
Moranda, Arianna
Falugi, Carla
author_facet Paladino, Ombretta
Moranda, Arianna
Falugi, Carla
author_sort Paladino, Ombretta
collection PubMed
description Awareness is growing that, besides several neurotoxic effects, cholinomimetic drugs able to interfere the cholinergic neurotransmitter system may exert a teratogen effect in developing embryos of vertebrate and invertebrate organisms. Cholinomimetic substances exert their toxic activity on organisms as they inhibit the functionality of the cholinergic system by completely or partially replacing the ACh molecule both at the level of the AChE active site and at the level of acetylcholine receptors. In this work, we focused the attention on the effects of muscarinic antagonist (atropine) and agonist (carbachol) drugs during the early development and ontogenesis of chick embryos. An unsteady-state mathematical model of the drug release and fate was developed, to synchronize exposure to a gradient of drug concentrations with the different developmental events. Since concentration measures in time and space cannot be taken without damaging the embryo itself, the diffusion model was the only way to establish at each time-step the exact concentration of drug at the different points of the embryo body (considered two-dimensional up to the 50 h stage). This concentration depends on the distance and position of the embryo with respect to the releasing source. The exposure to carbachol generally enhanced dimensions and stages of the embryos, while atropine mainly caused delay in development and small size of the embryos. Both the drugs were able to cause developmental anomalies, depending on the moment of development, in a time- and dose-dependent way, regardless the expression of genes driving each event. GRAPHICAL ABSTRACT: 1. Early chick embryos were exposed to muscarinic drugs in a spatial-temporal context. 2. Effects were stage-(time) dependent, according to distance and position of the source. 3. Atropine inhibited growth, mainly interfering with the cephalic process formation and heart differentiation; carbachol increased growth reducing differentiation. . 4. Interferences may be exerted by alteration of calcium responses to naturally occurring morphogen-driven mechanisms. . [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10565-022-09770-w.
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spelling pubmed-104254872023-08-16 Spatiotemporal role of muscarinic signaling in early chick development: exposure to cholinomimetic agents by a mathematical model Paladino, Ombretta Moranda, Arianna Falugi, Carla Cell Biol Toxicol Article Awareness is growing that, besides several neurotoxic effects, cholinomimetic drugs able to interfere the cholinergic neurotransmitter system may exert a teratogen effect in developing embryos of vertebrate and invertebrate organisms. Cholinomimetic substances exert their toxic activity on organisms as they inhibit the functionality of the cholinergic system by completely or partially replacing the ACh molecule both at the level of the AChE active site and at the level of acetylcholine receptors. In this work, we focused the attention on the effects of muscarinic antagonist (atropine) and agonist (carbachol) drugs during the early development and ontogenesis of chick embryos. An unsteady-state mathematical model of the drug release and fate was developed, to synchronize exposure to a gradient of drug concentrations with the different developmental events. Since concentration measures in time and space cannot be taken without damaging the embryo itself, the diffusion model was the only way to establish at each time-step the exact concentration of drug at the different points of the embryo body (considered two-dimensional up to the 50 h stage). This concentration depends on the distance and position of the embryo with respect to the releasing source. The exposure to carbachol generally enhanced dimensions and stages of the embryos, while atropine mainly caused delay in development and small size of the embryos. Both the drugs were able to cause developmental anomalies, depending on the moment of development, in a time- and dose-dependent way, regardless the expression of genes driving each event. GRAPHICAL ABSTRACT: 1. Early chick embryos were exposed to muscarinic drugs in a spatial-temporal context. 2. Effects were stage-(time) dependent, according to distance and position of the source. 3. Atropine inhibited growth, mainly interfering with the cephalic process formation and heart differentiation; carbachol increased growth reducing differentiation. . 4. Interferences may be exerted by alteration of calcium responses to naturally occurring morphogen-driven mechanisms. . [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10565-022-09770-w. Springer Netherlands 2022-09-13 2023 /pmc/articles/PMC10425487/ /pubmed/36098822 http://dx.doi.org/10.1007/s10565-022-09770-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Paladino, Ombretta
Moranda, Arianna
Falugi, Carla
Spatiotemporal role of muscarinic signaling in early chick development: exposure to cholinomimetic agents by a mathematical model
title Spatiotemporal role of muscarinic signaling in early chick development: exposure to cholinomimetic agents by a mathematical model
title_full Spatiotemporal role of muscarinic signaling in early chick development: exposure to cholinomimetic agents by a mathematical model
title_fullStr Spatiotemporal role of muscarinic signaling in early chick development: exposure to cholinomimetic agents by a mathematical model
title_full_unstemmed Spatiotemporal role of muscarinic signaling in early chick development: exposure to cholinomimetic agents by a mathematical model
title_short Spatiotemporal role of muscarinic signaling in early chick development: exposure to cholinomimetic agents by a mathematical model
title_sort spatiotemporal role of muscarinic signaling in early chick development: exposure to cholinomimetic agents by a mathematical model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425487/
https://www.ncbi.nlm.nih.gov/pubmed/36098822
http://dx.doi.org/10.1007/s10565-022-09770-w
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