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Pharmacological Dose-Effect Profiles of Various Concentrations of Humanised Primary Bile Acid in Encapsulated Cells
Bile acids (BA)s are known surfactants and well-documented to play a major role in food digestion and absorption. Recently, potential endocrinological and formulation-stabilisation effects of BAs have been explored and their pharmacological effects on supporting cell survival and functions have gain...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879575/ https://www.ncbi.nlm.nih.gov/pubmed/35214975 http://dx.doi.org/10.3390/nano12040647 |
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author | Mooranian, Armin Jones, Melissa Walker, Daniel Ionescu, Corina Mihaela Wagle, Susbin Raj Kovacevic, Bozica Chester, Jacqueline Foster, Thomas Johnston, Edan Kuthubutheen, Jafri Brown, Daniel Atlas, Marcus D. Mikov, Momir Al-Salami, Hani |
author_facet | Mooranian, Armin Jones, Melissa Walker, Daniel Ionescu, Corina Mihaela Wagle, Susbin Raj Kovacevic, Bozica Chester, Jacqueline Foster, Thomas Johnston, Edan Kuthubutheen, Jafri Brown, Daniel Atlas, Marcus D. Mikov, Momir Al-Salami, Hani |
author_sort | Mooranian, Armin |
collection | PubMed |
description | Bile acids (BA)s are known surfactants and well-documented to play a major role in food digestion and absorption. Recently, potential endocrinological and formulation-stabilisation effects of BAs have been explored and their pharmacological effects on supporting cell survival and functions have gained wide interest. Hence, this study aimed to explore the hyper-glycaemic dependent dose-effect of the BA chenodeoxycholic acid (CDCA) when encapsulated with pancreatic β-cells, allowing assessment of CDCA’s impacts when encapsulated. Four different concentrations of the BA were prepared, and viable cells were encapsulated and incubated for 2 days. Multiple analyses were carried out including confocal imaging, glucose-induced cellular mitochondrial viability indices, insulin production, inflammatory biomarker analyses and cellular bioenergetics measurements. There was a significant dose-effect with different concentrations of the BA, affecting cellular viability and antioxidant activities, cell functions and insulin release, inflammatory biomarkers, and cellular-bioenergetics at different oxidative stress levels. The results demonstrate that, when encapsulated, the BA CDCA exerts positive pharmacological effects at the cellular level, and such effects are concentration dependent. |
format | Online Article Text |
id | pubmed-8879575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88795752022-02-26 Pharmacological Dose-Effect Profiles of Various Concentrations of Humanised Primary Bile Acid in Encapsulated Cells Mooranian, Armin Jones, Melissa Walker, Daniel Ionescu, Corina Mihaela Wagle, Susbin Raj Kovacevic, Bozica Chester, Jacqueline Foster, Thomas Johnston, Edan Kuthubutheen, Jafri Brown, Daniel Atlas, Marcus D. Mikov, Momir Al-Salami, Hani Nanomaterials (Basel) Article Bile acids (BA)s are known surfactants and well-documented to play a major role in food digestion and absorption. Recently, potential endocrinological and formulation-stabilisation effects of BAs have been explored and their pharmacological effects on supporting cell survival and functions have gained wide interest. Hence, this study aimed to explore the hyper-glycaemic dependent dose-effect of the BA chenodeoxycholic acid (CDCA) when encapsulated with pancreatic β-cells, allowing assessment of CDCA’s impacts when encapsulated. Four different concentrations of the BA were prepared, and viable cells were encapsulated and incubated for 2 days. Multiple analyses were carried out including confocal imaging, glucose-induced cellular mitochondrial viability indices, insulin production, inflammatory biomarker analyses and cellular bioenergetics measurements. There was a significant dose-effect with different concentrations of the BA, affecting cellular viability and antioxidant activities, cell functions and insulin release, inflammatory biomarkers, and cellular-bioenergetics at different oxidative stress levels. The results demonstrate that, when encapsulated, the BA CDCA exerts positive pharmacological effects at the cellular level, and such effects are concentration dependent. MDPI 2022-02-15 /pmc/articles/PMC8879575/ /pubmed/35214975 http://dx.doi.org/10.3390/nano12040647 Text en © 2022 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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mooranian, Armin Jones, Melissa Walker, Daniel Ionescu, Corina Mihaela Wagle, Susbin Raj Kovacevic, Bozica Chester, Jacqueline Foster, Thomas Johnston, Edan Kuthubutheen, Jafri Brown, Daniel Atlas, Marcus D. Mikov, Momir Al-Salami, Hani Pharmacological Dose-Effect Profiles of Various Concentrations of Humanised Primary Bile Acid in Encapsulated Cells |
title | Pharmacological Dose-Effect Profiles of Various Concentrations of Humanised Primary Bile Acid in Encapsulated Cells |
title_full | Pharmacological Dose-Effect Profiles of Various Concentrations of Humanised Primary Bile Acid in Encapsulated Cells |
title_fullStr | Pharmacological Dose-Effect Profiles of Various Concentrations of Humanised Primary Bile Acid in Encapsulated Cells |
title_full_unstemmed | Pharmacological Dose-Effect Profiles of Various Concentrations of Humanised Primary Bile Acid in Encapsulated Cells |
title_short | Pharmacological Dose-Effect Profiles of Various Concentrations of Humanised Primary Bile Acid in Encapsulated Cells |
title_sort | pharmacological dose-effect profiles of various concentrations of humanised primary bile acid in encapsulated cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879575/ https://www.ncbi.nlm.nih.gov/pubmed/35214975 http://dx.doi.org/10.3390/nano12040647 |
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