The Effects of Different Respiratory Viruses on the Oxidative Stress Marker Levels in an In Vitro Model: A Pilot Study
- 1Faculty of Veterinary Medicine, Department of Pathology, Division of Microbiology, Wrocław University of Environmental and Life Sciences, 50-375 Wrocław, Poland.
- 2Department of Physiology in Zabrze, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, 40-055 Katowice, Poland.
- 3Department of Natural Sciences, Institute of Biology, Biotechnology and Environmental Protection, University of Silesia in Katowice, 40-007 Katowice, Poland.
- 4Department of Medical Statistics, Faculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia, 40-055 Katowice, Poland.
- 5Department of Internal Medicine and Geriatrics, Faculty of Medicine, Jagiellonian University Medical College, 31-688 Kraków, Poland.
- 6Department of Endoscopy, University Hospital, 30-688 Kraków, Poland.
- 0Faculty of Veterinary Medicine, Department of Pathology, Division of Microbiology, Wrocław University of Environmental and Life Sciences, 50-375 Wrocław, Poland.
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View abstract on PubMed
Summary
This summary is machine-generated.Respiratory viral infections impact oxidative stress differently in normal versus tumor lung cells. Tumor cells showed greater changes in non-enzymatic markers, while normal cells exhibited broader alterations.
Area Of Science
- Biochemistry
- Cell Biology
- Virology
Background
- Respiratory viruses are common causes of human infections.
- Oxidative stress alterations are significant in viral infections.
- Understanding these changes is crucial for treatment and therapeutics.
Purpose Of The Study
- To compare oxidative stress markers in normal (MRC-5) and tumor (A549) lung cells.
- To investigate the effects of human coronaviruses (HCoV) OC43 and 229E, human adenovirus type 5 (HAdV5), and human rhinovirus A (HRV A).
- To analyze total oxidative status (TOS), total antioxidant capacity (TAC), oxidative stress index (OSI), glutathione peroxidase (GPx), and glutathione reductase (GR).
Main Methods
- Infection of MRC-5 and A549 cell lines with HCoV OC43, HCoV 229E, HAdV5, and HRV A.
- Measurement of TOS, TAC, and OSI levels.
- Assay of GPx and GR enzyme activities.
Main Results
- Respiratory viral infections differentially affected oxidative stress markers in lung cell lines.
- A549 (tumor) cells showed more significant alterations in non-enzymatic oxidative stress markers.
- MRC-5 (normal) cells displayed changes in both enzymatic and non-enzymatic oxidative stress markers.
Conclusions
- Viral infections induce distinct oxidative stress responses in normal and cancerous lung cells.
- Lung adenocarcinoma cells (A549) are more sensitive to non-enzymatic oxidative stress changes.
- Further research is needed to elucidate these differential responses.
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