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Direct Contraction Force Measurements of Engineered Cardiac Tissue Constructs With Inotropic Drug Exposure
Contractility is one of the most crucial functions of the heart because it is directly related to the maintenance of blood perfusion throughout the body. Both increase and decrease in contractility may cause fatal consequences. Therefore, drug discovery would benefit greatly from reliable testing of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110810/ https://www.ncbi.nlm.nih.gov/pubmed/35592423 http://dx.doi.org/10.3389/fphar.2022.871569 |
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author | Koivisto, Maria Mosallaei, Milad Toimela, Tarja Tuukkanen, Sampo Heinonen, Tuula |
author_facet | Koivisto, Maria Mosallaei, Milad Toimela, Tarja Tuukkanen, Sampo Heinonen, Tuula |
author_sort | Koivisto, Maria |
collection | PubMed |
description | Contractility is one of the most crucial functions of the heart because it is directly related to the maintenance of blood perfusion throughout the body. Both increase and decrease in contractility may cause fatal consequences. Therefore, drug discovery would benefit greatly from reliable testing of candidate molecule effects on contractility capacity. In this study, we further developed a dual-axis piezoelectric force sensor together with our human cell–based vascularized cardiac tissue constructs for cardiac contraction force measurements. The capability to detect drug-induced inotropic effects was tested with a set of known positive and negative inotropic compounds of isoprenaline, milrinone, omecamtiv mecarbil, propranolol, or verapamil in different concentrations. Both positive and negative inotropic effects were measurable, showing that our cardiac contraction force measurement system including a piezoelectric cantilever sensor and a human cell–based cardiac tissue constructs has the potential to be used for testing of inotropic drug effects. |
format | Online Article Text |
id | pubmed-9110810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91108102022-05-18 Direct Contraction Force Measurements of Engineered Cardiac Tissue Constructs With Inotropic Drug Exposure Koivisto, Maria Mosallaei, Milad Toimela, Tarja Tuukkanen, Sampo Heinonen, Tuula Front Pharmacol Pharmacology Contractility is one of the most crucial functions of the heart because it is directly related to the maintenance of blood perfusion throughout the body. Both increase and decrease in contractility may cause fatal consequences. Therefore, drug discovery would benefit greatly from reliable testing of candidate molecule effects on contractility capacity. In this study, we further developed a dual-axis piezoelectric force sensor together with our human cell–based vascularized cardiac tissue constructs for cardiac contraction force measurements. The capability to detect drug-induced inotropic effects was tested with a set of known positive and negative inotropic compounds of isoprenaline, milrinone, omecamtiv mecarbil, propranolol, or verapamil in different concentrations. Both positive and negative inotropic effects were measurable, showing that our cardiac contraction force measurement system including a piezoelectric cantilever sensor and a human cell–based cardiac tissue constructs has the potential to be used for testing of inotropic drug effects. Frontiers Media S.A. 2022-05-03 /pmc/articles/PMC9110810/ /pubmed/35592423 http://dx.doi.org/10.3389/fphar.2022.871569 Text en Copyright © 2022 Koivisto, Mosallaei, Toimela, Tuukkanen and Heinonen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Koivisto, Maria Mosallaei, Milad Toimela, Tarja Tuukkanen, Sampo Heinonen, Tuula Direct Contraction Force Measurements of Engineered Cardiac Tissue Constructs With Inotropic Drug Exposure |
title | Direct Contraction Force Measurements of Engineered Cardiac Tissue Constructs With Inotropic Drug Exposure |
title_full | Direct Contraction Force Measurements of Engineered Cardiac Tissue Constructs With Inotropic Drug Exposure |
title_fullStr | Direct Contraction Force Measurements of Engineered Cardiac Tissue Constructs With Inotropic Drug Exposure |
title_full_unstemmed | Direct Contraction Force Measurements of Engineered Cardiac Tissue Constructs With Inotropic Drug Exposure |
title_short | Direct Contraction Force Measurements of Engineered Cardiac Tissue Constructs With Inotropic Drug Exposure |
title_sort | direct contraction force measurements of engineered cardiac tissue constructs with inotropic drug exposure |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110810/ https://www.ncbi.nlm.nih.gov/pubmed/35592423 http://dx.doi.org/10.3389/fphar.2022.871569 |
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