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Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells
INTRODUCTION: Inosine pranobex (Isoprinosine) stimulates cell-mediated immune responses to viral infections in humans and might have also therapeutic use in animals. The aim of this study was to compare three in vitro cytotoxicity assays on mouse embryo fibroblasts and liver cancer cells and determi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sciendo
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200297/ https://www.ncbi.nlm.nih.gov/pubmed/30364913 http://dx.doi.org/10.2478/jvetres-2018-0031 |
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author | Tobólska, Sylwia Terpiłowska, Sylwia Jaroszewski, Jerzy Siwicki, Andrzej Krzysztof |
author_facet | Tobólska, Sylwia Terpiłowska, Sylwia Jaroszewski, Jerzy Siwicki, Andrzej Krzysztof |
author_sort | Tobólska, Sylwia |
collection | PubMed |
description | INTRODUCTION: Inosine pranobex (Isoprinosine) stimulates cell-mediated immune responses to viral infections in humans and might have also therapeutic use in animals. The aim of this study was to compare three in vitro cytotoxicity assays on mouse embryo fibroblasts and liver cancer cells and determine their ability to detect early cytotoxic effects for inosine pranobex. MATERIAL AND METHODS: BALB/3T3 clone A31and HepG2 cells were incubated with inosine pranobex at concentrations from 0.1 to 1,000 μg/mL. Cell viability was determined with the MTT reduction, the LHD release, and the NRU tests. RESULTS: A decrease in the cell viability was observed after incubating the BALB/3T3 clone A31and HepG2 cells with inosine pranobex. CONCLUSIONS: Based on the cytotoxicity endpoints measured in these investigations in BALB/3T3 clone A31cells, it can be concluded that the cell membrane may be the first part of the cell to be affected by inosine pranobex. The disintegration of lysosomes and mitochondria follows mitochondria damage. In HepG2 cells likewise, the cell membrane may be the first part of the cell to be affected by inosine pranobex. Also in liver cancer cells, the disintegration of mitochondria (assessed with the MTT reduction assay) and next of lysosomes (assessed with the NRU assay) follows mitochondria damage. |
format | Online Article Text |
id | pubmed-6200297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Sciendo |
record_format | MEDLINE/PubMed |
spelling | pubmed-62002972018-10-25 Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells Tobólska, Sylwia Terpiłowska, Sylwia Jaroszewski, Jerzy Siwicki, Andrzej Krzysztof J Vet Res Research Article INTRODUCTION: Inosine pranobex (Isoprinosine) stimulates cell-mediated immune responses to viral infections in humans and might have also therapeutic use in animals. The aim of this study was to compare three in vitro cytotoxicity assays on mouse embryo fibroblasts and liver cancer cells and determine their ability to detect early cytotoxic effects for inosine pranobex. MATERIAL AND METHODS: BALB/3T3 clone A31and HepG2 cells were incubated with inosine pranobex at concentrations from 0.1 to 1,000 μg/mL. Cell viability was determined with the MTT reduction, the LHD release, and the NRU tests. RESULTS: A decrease in the cell viability was observed after incubating the BALB/3T3 clone A31and HepG2 cells with inosine pranobex. CONCLUSIONS: Based on the cytotoxicity endpoints measured in these investigations in BALB/3T3 clone A31cells, it can be concluded that the cell membrane may be the first part of the cell to be affected by inosine pranobex. The disintegration of lysosomes and mitochondria follows mitochondria damage. In HepG2 cells likewise, the cell membrane may be the first part of the cell to be affected by inosine pranobex. Also in liver cancer cells, the disintegration of mitochondria (assessed with the MTT reduction assay) and next of lysosomes (assessed with the NRU assay) follows mitochondria damage. Sciendo 2018-10-24 /pmc/articles/PMC6200297/ /pubmed/30364913 http://dx.doi.org/10.2478/jvetres-2018-0031 Text en © 2018 Sylwia Tobólska et al., published by Sciendo http://creativecommons.org/licenses/by-nc-nd/3.0 This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License. |
spellingShingle | Research Article Tobólska, Sylwia Terpiłowska, Sylwia Jaroszewski, Jerzy Siwicki, Andrzej Krzysztof Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells |
title | Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells |
title_full | Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells |
title_fullStr | Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells |
title_full_unstemmed | Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells |
title_short | Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells |
title_sort | influence of inosine pranobex on cell viability in normal fibroblasts and liver cancer cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200297/ https://www.ncbi.nlm.nih.gov/pubmed/30364913 http://dx.doi.org/10.2478/jvetres-2018-0031 |
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