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In vivo dose–response analysis to acetylcholine: pharmacodynamic assessment by polarized reflectance spectroscopy

Transdermal iontophoresis offers an in vivo alternative to the strain-gauge model for measurement of vascular function but is limited due to lack of technical solutions for outcome assessment. The aims of this study were to, after measurement by polarized reflectance spectroscopy (PRS), use pharmaco...

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Autores principales: Henricson, Joakim, Sjöberg, Folke, Iredahl, Fredrik, Strömberg, Tomas, Wilhelms, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023454/
https://www.ncbi.nlm.nih.gov/pubmed/35449189
http://dx.doi.org/10.1038/s41598-022-10617-x
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author Henricson, Joakim
Sjöberg, Folke
Iredahl, Fredrik
Strömberg, Tomas
Wilhelms, Daniel
author_facet Henricson, Joakim
Sjöberg, Folke
Iredahl, Fredrik
Strömberg, Tomas
Wilhelms, Daniel
author_sort Henricson, Joakim
collection PubMed
description Transdermal iontophoresis offers an in vivo alternative to the strain-gauge model for measurement of vascular function but is limited due to lack of technical solutions for outcome assessment. The aims of this study were to, after measurement by polarized reflectance spectroscopy (PRS), use pharmacodynamic dose–response analysis on responses to different concentrations of acetylcholine (ACh); and to examine the effect of three consecutively administered iontophoretic current pulses. The vascular responses in 15 healthy volunteers to iontophorised ACh (5 concentrations, range 0.0001% to 1%, three consecutive pulses of 0.02 mA for 10 min each) were recorded using PRS. Data were fitted to a four-parameter logistic dose response model and compared. Vascular responses were quantifiable by PRS. Similar pharmacodynamic dose response curves could be generated irrespectively of the ACh concentration. Linearly increasing maximum vasodilatory responses were registered with increasing concentration of ACh. A limited linear dose effect of the concentration of ACh was seen between pulses. Polarized reflectance spectroscopy is well suited for measuring vascular responses to iontophoretically administrated ACh. The results of this study support further development of iontophoresis as a method to study vascular function and pharmacological responses in vivo.
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spelling pubmed-90234542022-04-25 In vivo dose–response analysis to acetylcholine: pharmacodynamic assessment by polarized reflectance spectroscopy Henricson, Joakim Sjöberg, Folke Iredahl, Fredrik Strömberg, Tomas Wilhelms, Daniel Sci Rep Article Transdermal iontophoresis offers an in vivo alternative to the strain-gauge model for measurement of vascular function but is limited due to lack of technical solutions for outcome assessment. The aims of this study were to, after measurement by polarized reflectance spectroscopy (PRS), use pharmacodynamic dose–response analysis on responses to different concentrations of acetylcholine (ACh); and to examine the effect of three consecutively administered iontophoretic current pulses. The vascular responses in 15 healthy volunteers to iontophorised ACh (5 concentrations, range 0.0001% to 1%, three consecutive pulses of 0.02 mA for 10 min each) were recorded using PRS. Data were fitted to a four-parameter logistic dose response model and compared. Vascular responses were quantifiable by PRS. Similar pharmacodynamic dose response curves could be generated irrespectively of the ACh concentration. Linearly increasing maximum vasodilatory responses were registered with increasing concentration of ACh. A limited linear dose effect of the concentration of ACh was seen between pulses. Polarized reflectance spectroscopy is well suited for measuring vascular responses to iontophoretically administrated ACh. The results of this study support further development of iontophoresis as a method to study vascular function and pharmacological responses in vivo. Nature Publishing Group UK 2022-04-21 /pmc/articles/PMC9023454/ /pubmed/35449189 http://dx.doi.org/10.1038/s41598-022-10617-x Text en © The Author(s) 2022 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 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
Henricson, Joakim
Sjöberg, Folke
Iredahl, Fredrik
Strömberg, Tomas
Wilhelms, Daniel
In vivo dose–response analysis to acetylcholine: pharmacodynamic assessment by polarized reflectance spectroscopy
title In vivo dose–response analysis to acetylcholine: pharmacodynamic assessment by polarized reflectance spectroscopy
title_full In vivo dose–response analysis to acetylcholine: pharmacodynamic assessment by polarized reflectance spectroscopy
title_fullStr In vivo dose–response analysis to acetylcholine: pharmacodynamic assessment by polarized reflectance spectroscopy
title_full_unstemmed In vivo dose–response analysis to acetylcholine: pharmacodynamic assessment by polarized reflectance spectroscopy
title_short In vivo dose–response analysis to acetylcholine: pharmacodynamic assessment by polarized reflectance spectroscopy
title_sort in vivo dose–response analysis to acetylcholine: pharmacodynamic assessment by polarized reflectance spectroscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023454/
https://www.ncbi.nlm.nih.gov/pubmed/35449189
http://dx.doi.org/10.1038/s41598-022-10617-x
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