Preview

Bulletin Physiology and Pathology of Respiration

Advanced search

Oxidative stress in peripheral blood leukocytes of patients with chronic obstructive pulmonary disease

https://doi.org/10.36604/1998-5029-2023-87-62-70

Abstract

Introduction. It is known that oxidative stress causes pathological changes in the tissues and organs of the human body and in many cases it can explain the disorders associated with chronic obstructive pulmonary disease (COPD).

Aim. The aim of the study was to investigate the degree of oxidative stress in peripheral blood leukocytes of COPD patients.

Materials and methods. We examined 23 patients with COPD of varying severity, 8 smokers without signs of bronchial obstruction and 9 healthy volunteers who had never smoked. All subjects underwent spirometry to assess lung function. The level of oxidative stress was determined using flow cytometry by adding 10 µM 2',7'-dichloro dihydrofluorescein diacetate to isolated peripheral blood leukocytes, in basal conditions and under pro-inflammatory stimulation with 0.1 ng/ml phorbol-12-myristate-13-acetate (PMA).

Results. Patients with COPD demonstrated elevated levels of intracellular oxidative stress compared with controls both under basal conditions and during PMA stimulation (p<0.05). When analyzed in subgroups, stimulation led to a significant increase in oxidative stress regardless of cell type (p<0.01). Smokers tend to have elevated measured values, occupying an intermediate position between non-smokers and COPD patients. The absolute increase in the oxidative stress index was higher in the cells of COPD patients; the values of the relative increase were almost identical in the studied groups. The dynamics of oxidative stress in the cells of smokers tended to be more pronounced than in non-smokers.

Conclusion. The obtained results indicate that the leukocytes of COPD patients are characterized by a higher level of intracellular oxidative stress. In addition, smoking has been found to be a factor of oxidative stress development in healthy individuals.

About the Authors

O. O. Kotova
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Olesya O. Kotova - PhD (Med.), Junior Staff Scientist, Laboratory of Molecular and Translational Research.

22 Kalinina Str., Blagoveshchensk, 675000



D. A. Gassan
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Dina A. Gassan - PhD (Med.), Staff Scientist, Laboratory of Molecular and Translational Research.

22 Kalinina Str., Blagoveshchensk, 675000



I. Yu. Sugaylo
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Ivana Yu. Sugaylo - Junior Staff Scientist, Laboratory of Molecular and Translational Research.

22 Kalinina Str., Blagoveshchensk, 675000



D. E. Naumov
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Denis E. Naumov - PhD (Med.), Head of Laboratory of Molecular and Translational Research.

22 Kalinina Str., Blagoveshchensk, 675000



Y. G. Gorchakova
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Yana G. Gorchakova - Research Laboratory Assistant, Laboratory of Molecular and Translational Research.

22 Kalinina Str., Blagoveshchensk, 675000



E. G. Sheludko
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Elizaveta G. Sheludko - PhD (Med.), Staff Scientist, Laboratory of Molecular and Translational Research.

22 Kalinina Str., Blagoveshchensk, 675000



References

1. Adeloye D., Song P., Zhu Y., Campbell H., Sheikh A., Rudan I.; NIHR RESPIRE Global Respiratory Health Unit. Global, regional, and national prevalence of, and risk factors for, chronic obstructive pulmonary disease (COPD) in 2019: a systematic review and modelling analysis. Lancet Respir. Med. 2022; 10(5):447–458. https://doi.org/10.1016/S22132600(21)00511-7

2. Herb M., Gluschko A., Schramm M. Reactive Oxygen Species: Not Omnipresent but Important in Many Locations. Front. Cell Dev. Biol. 2021; 9:716406. https://doi.org/10.3389/fcell.2021.716406

3. Herb M., Schramm M. Functions of ROS in Macrophages and Antimicrobial Immunity. Antioxidants (Basel) 2021; 10(2):313. https://doi.org/10.3390/antiox10020313

4. Mills E.L., Kelly B., Logan A., Costa A.S.H., Varma M., Bryant C.E., Tourlomousis P., Däbritz J.H.M., Gottlieb E., Latorre I., Corr S.C., McManus G., Ryan D., Jacobs H.T., Szibor M., Xavier R.J., Braun T., Frezza C., Murphy M.P., O'Neill L.A. Succinate Dehydrogenase Supports Metabolic Repurposing of Mitochondria to Drive Inflammatory Macrophages. Cell 2016; 167(2):457–470.e13. https://doi.org/10.1016/j.cell.2016.08.064

5. Rogers L.K., Cismowski M.J. Oxidative stress in the lung ‒ the essential paradox. Curr. Opin. Toxicol. 2018; 7:37– 43. https://doi.org/10.1016/j.cotox.2017.09.001

6. Liu X., Chen Z. The pathophysiological role of mitochondrial oxidative stress in lung diseases. J. Transl. Med. 2017; 15(1):207. https://doi.org/10.1186/s12967-017-1306-5

7. Bhandary B., Marahatta A., Kim H.R., Chae H.J. An involvement of oxidative stress in endoplasmic reticulum stress and its associated diseases. Int. J. Mol. Sci. 2012; 14(1):434–456. https://doi.org/10.3390/ijms14010434

8. Afanas'ev I. New nucleophilic mechanisms of ros-dependent epigenetic modifications: comparison of aging and cancer. Aging Dis. 2014; 5(1):52–62. https://doi.org/10.14336/AD.2014.050052

9. Richter K., Konzack A., Pihlajaniemi T., Heljasvaara R., Kietzmann T. Redox-fibrosis: impact of TGFβ1 on ROS generators, mediators and functional consequences. Redox Biol. 2015; 6:344–352. https://doi.org/10.1016/j.redox.2015.08.015

10. Shao M.X., Nadel J.A. Dual oxidase 1-dependent MUC5AC mucin expression in cultured human airway epithelial cells. Proc. Natl Acad. Sci. USA 2005; 102(3):767–772. https://doi.org/10.1073/pnas.0408932102

11. Barnes P.J. COPD 2020: new directions needed. Am. J. Physiol. Lung Cell. Mol. Physiol. 2020; 319(5):L884– L886. doi: 10.1152/ajplung.00473.2020

12. Barnes P.J. Oxidative Stress in Chronic Obstructive Pulmonary Disease. Antioxidants (Basel) 2022; 11(5):965. https://doi.org/10.3390/antiox11050965

13. Al-Azzawi M.A., Alaa A., Ghoneim A.H.A., Abozaid M.M.N. The effect of cigarette smoking on the oxidant–antioxidant imbalance in patients with chronic obstructive pulmonary disease. Egypt. J. Chest Dis. Tuberc. 2019. 68(4):462‒470. https://doi.org/10.4103/ejcdt.ejcdt_184_18

14. Zheng J.P., Wen F.Q., Bai C.X., Wan H.Y., Kang J., Chen P., Yao W.Z., Ma L.J., Xia Q.K., Gao Y., Zhong N.S.; PANTHEON study committee. High-dose N-acetylcysteine in the prevention of COPD exacerbations: rationale and design of the PANTHEON Study. COPD 2013; 10(2):164–171. https://doi.org/10.3109/15412555.2012.732628

15. Tse H.N., Raiteri L., Wong K.Y., Yee K.S., Ng L.Y., Wai K.Y., Loo C.K., Chan M.H. High-dose N-acetylcysteine in stable COPD: the 1-year, double-blind, randomized, placebo-controlled HIACE study. Chest 2013; 144(1):106–118. https://doi.org/10.1378/chest.12-2357

16. Paudel K.R., Panth N., Manandhar B., Singh S.K., Gupta G., Wich P.R., Nammi S., MacLoughlin R., Adams J., Warkiani M.E., Chellappan D.K., Oliver B.G., Hansbro P.M., Dua K. Attenuation of Cigarette-Smoke-Induced Oxidative Stress, Senescence, and Inflammation by Berberine-Loaded Liquid Crystalline Nanoparticles: In Vitro Study in 16HBE and RAW264.7 Cells. Antioxidants 2022; 11(5):873. https://doi.org/10.3390/antiox11050873


Review

For citations:


Kotova O.O., Gassan D.A., Sugaylo I.Yu., Naumov D.E., Gorchakova Y.G., Sheludko E.G. Oxidative stress in peripheral blood leukocytes of patients with chronic obstructive pulmonary disease. Bulletin Physiology and Pathology of Respiration. 2023;(87):62-70. (In Russ.) https://doi.org/10.36604/1998-5029-2023-87-62-70

Views: 194


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1998-5029 (Print)