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Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells. | LitMetric

Influence of Inosine Pranobex on Cell Viability in Normal Fibroblasts and Liver Cancer Cells.

J Vet Res

Department of Microbiology and Clinical Immunology, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, 10-957 Olsztyn, Poland.

Published: June 2018

AI Article Synopsis

  • * The study compared three cytotoxicity assays (MTT reduction, LHD release, NRU tests) on mouse embryo fibroblasts and liver cancer cells treated with varying concentrations of inosine pranobex.
  • * Findings indicated that inosine pranobex reduces cell viability, starting with damage to the cell membrane, followed by organelle disintegration in both BALB/3T3 and HepG2 cells.

Article Abstract

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 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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6200297PMC
http://dx.doi.org/10.2478/jvetres-2018-0031DOI Listing

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