TIME DYNAMICS OF PRODUCTION OF REACTIVE OXYGEN SPECIES BY NEUTROPHILS AFTER TREATMENT UNDER HYPOMAGNETIC CONDITIONS
Abstract and keywords
Abstract (English):
. It was shown that incubation of a suspension of mouse peritoneal neutrophils for 30 minutes under hypomagnetic conditions obtained using permalloy magnetic screens (a constant magnetic field of not more than 20 nT, the level of variable man-made noise is reduced to a few nT) causes a significant decrease (about 48%) signal intensity of lucigenin-dependent chemiluminescence measured immediately after incubation. 20 minutes after magnetic treatment (followed by incubation in a geomagnetic field during this time, induction 44 μT, the level of magnetic interference at a frequency of 50 Hz was 15-50 nT), the differences between the control and experimental groups remain completely (the difference was about 49%). In 40 and 60 minutes after exposure to the "zero" field, followed by keeping the samples in the geomagnetic field for the specified time intervals, the difference between the control and experimental samples decreased to 32% and 22%, respectively. This effect was registered without additional activation of neutrophils by chemical agents initiating respiratory burst, such as N-formyl-Met-Leu-Phe formylated peptide or phorbol-12-meristat-13-acetate phorbol ester, and was not associated with effects on cellular systems, providing this explosion.

Keywords:
hypomagnetic field, geomagnetic field, neutrophils, reactive oxygen species, lucigenin, chemiluminescence
Text
Publication text (PDF): Read Download
References

1. Zhang H., Zhang Z., Mo W. et al. Shielding of the geomagnetic field reduces hydrogen peroxide production in human neuroblastoma cell and inhibits the activity of CuZn superoxide dismutase. Protein Cell, 2017, vol. 8, no. 7, pp. 527-537.

2. Martino C.F., Castello P.R. Modulation of hydrogen peroxide production in cellular systems by low level magnetic fields. PLoS ONE, 2011, vol. 6, no. 8, e22753.

3. Politanski P., Rajkowska E., Brodecki M. et al. Combined effect of X-ray radiation and static magnetic fields on reactive oxygen species in rat lymphocytes in vitro. Bioelectromagnetics, 2013, vol. 34, pp. 333-336.

4. Binhi V.N., Prato F.S. Biological effects of the hypomagnetic field: Analytical review of experiments and theories. PLoS ONE, 2017, vol. 12, no. 6, e0179340.

5. Zhang B., Tian L. Reactive oxygen species: potential regulatory molecules in response to hypomagnetic field exposure. Bioelectromagnetics, 2020, vol. 41, no. 8, pp. 573-580.

6. Novikov V.V., Yablokova E.V., Fesenko E.E. The effect of a «zero» magnetic field on the production of reactive oxygen species in neutrophils. Biophysics, 2018. vol. 63, no. 3, pp. 365-368. (In Russ.)

7. Novikov V.V., Yablokova E.V., Valeeva E.R., Fesenko E.E. On the molecular mechanisms of the effect of a zero magnetic field on the production of reactive oxygen species in inactivated neutrophils. Biophysics, 2019, vol. 64, no. 4, pp. 371-375. (In Russ.)

8. Novikov V.V., Yablokova E.V., Shaev I.A., Fesenko E.E. The effect of a weak static magnetic field in the range of magnitudes from a “Zero” Field (0.01 µT) to 100 µT on the production of reactive oxygen species in nonactivated neutrophils. Biophysics, 2020, vol. 65, no. 3, pp. 443-447. (In Russ.)

9. Aasen T.B., Bolann B., Glette J., Ulvik R.J., Schreiner A. Lucigenin-dependent chemiluminescence in mononuclear phagocytes. Role of superoxide anion. Scand. J. Clin. Lab. Invest., 1987, vol. 47, pp. 673-679.

10. Dzhatdoeva A.A., Proskurnina E.V., Nesterova A.M. et al. Mitochondria as a Source of Superoxide Anion Radical in Human Platelets. Biochemistry, 2018, vol. 12, pp. 43-49. (In Russ.)

11. Novikov V.V., Yablokova E.V., Shaev I.A., Fesenko E.E. Decreased production of the superoxide anion radical in neutrophils exposed to a near-null magnetic field. Biophysics, 2020, vol. 65, no. 4, pp. 625-630. (In Russ.)

12. Novikov V.V., Yablokova E.V., Fesenko E.E. A decrease of the respiratory burst in neutrophils after exposure to weak combined magnetic fields of a certain duration. Biophysics, 2020, vol. 65, no. 1, pp. 82-87. (In Russ.)

13. Barnes F., Kandala S. Effects of time delays on biological feedback systems and electromagnetic field exposures. Bioelectromagnetics, 2018, vol. 39, pp. 249-252.

14. Barnes F., Greenebaum B. Setting Guidelines for Electromagnetic Exposures and Research Needs. Bioelectromagnetics, 2020, vol. 41, pp. 392-397.

15. Osipenko M., Mezhevikina L., Krasts I., Yashin V., Novikov V., Fesenko E. Deterioration of murine embryonic fibroblasts and early embryos upon magnetic field deprivation. Biophysics, 2008, vol. 53, pp. 317-321.

16. Trukhanov K., Gur'eva T., Dadasheva O., Kruglov O., Lebedev V., Spasskii A. Embryogenesis of the Japanese quail in hypomagnetic conditions applied to deep space flights. Radiats Biol Radioecol, 2014, vol. 54, pp. 179-185.

17. Krylov V.V., Osipova E.A., Pankova N.A., Talikina M.G., Chebotareva Y.V., Izyumov Y.G., Nepomnyashchikh V.A., Batrakova A.A. The effect of a temporal shift in diurnal geomagnetic variation on roach Rutilus Rutilus L. embryos: a comparison with effects of simulated geomagnetic storms. Biophysics, 2017, vol. 62, no. 4, pp. 675-681. (In Russ.)

18. Novikov V.V., Sheiman I.M., Fesenko E.E. The effect of weak and superweak constant magnetic fields on the intensity of asexual reproduction of Dugesia tigrina planarians. Biophysics, 2007, vol. 52, iss. 5, pp. 912-915. (In Russ.)

19. Novikov V.V., Sheiman I.M., Fesenko E.E. Effect of weak static and low-frequency alternating magnetic fields on the fission and regeneration of the planarian Dugesia (Girardia) tigrine. Bioelectromagnetics, 2008, vol. 29, pp. 387-393.

20. Van Huizen A.V., Morton J.M., Kinsey L.J., Von Kannon D.G., Saad M.A., Birkholz T.R., Czajka J.M., Cyrus J., Barnes F.S., Beane W.S. Weak magnetic fields alter stem cell -mediated growth. Sci Adv, 2019, vol. 5, eaau7201.

21. Lednev V.V., Srebnitskaya L.K., Ilyasova E.N., Rozhdestvenskaya Z.E., Klimov A.A., Tiras Kh.P. A weak combined magnetic field tuned to the permetric resonance of nuclear spins of hydrogen atoms increases the proliferative activity of neoblasts in the regenerating planaria Dugesia tigrina. DAN, 1996, vol. 348, iss. 6, pp. 830-833 (In Russ.)

22. Tiras Kh.P., Petrova O.N., Myakisheva S.N., Aslanidi K.B. Biological effects of weak magnetic fields: a comparative analysis. Basic research, 2014, no. 12 (part 7), pp. 1442-1451. (In Russ.)

23. Zhang B., Lu H., Xi W., Zhou X., Xu S., Zhang K., Guo A. Exposure to hypomagnetic field space for multiple generations causes amnesia in Drosophila melanogaster. Neurosci Lett, 2004, vol. 371, pp. 190-195.

24. Binhi V.N., Sarimov R.M. Zero magnetic field effect observed in human cognitive processes. Electromagn Biol Med, 2009, vol. 28, pp. 310-315.

25. Barnes F., Greenebaum B. The effects of weak magnetic fields on radical pairs. Bioelectromagnetics, 2015, vol. 36, pp. 45-54.

26. Ponomarev V.O., Novikov V.V. Effect of low-frequency alternating magnetic fields on the rate of biochemical reactions proceeding with formation of reactive oxygen species. Biophysics, 2009, vol. 54, pp. 163-168.


Login or Create
* Forgot password?