Preview

Сибирский научный медицинский журнал

Advanced search

Cytoprotective effect of non-opiate leu-enkephalin analogues against the background of ornithine decarboxylase inhibitor exposure

https://doi.org/10.18699/SSMJ20240615

Abstract

The purpose of the study was to assess the involvement of the polyamine system in the implementation of the cytoprotective effect of non-opiate analogues of leu-enkephalin under conditions of oxidative stress. Material and methods. Rat pulmonary fibroblasts were incubated with the NALE peptide (Phe–D-Ala–Gly–Phe–Leu–Arg, 0.1 μM) and its structural analogue peptide G (Phe–D-Ala–Gly–Phe–Leu–Gly, 0. 1 µM), some series - with difluoromethylornithine (DFMO, 2 mM). Oxidative stress was modeled by adding H2O2 (100 μM) to the culture medium. The morphometric parameters of the nucleo-nucleolar apparatus of fibroblasts, the proliferative activity of cells, and the features of p53 expression were studied on monolayers. Results. Incubation of fibroblasts with hydrogen peroxide leads to a stress response of cells, as evidenced by the complete absence of mitotic activity, a significant decrease in cell culture density, an increase in the area of nuclei and an increase in the proportion of p53 + fibroblasts. Incubation with the ornithine decarboxylase synthesis blocker DFMO caused a deterioration in the condition of the cell culture: the mitotic index decreased, and the number of p53 + fibroblasts increased even more significantly. Pre-incubation (before adding H2O2) with NALE and G peptides reduced, but did not completely eliminate, the negative effect of hydrogen peroxide on cell culture. Preliminary co-incubation of cell monolayers with peptides and DFMO showed a more pronounced cytoprotective effect in OS. Thus, in the series with NALE, the indicators of the proportion of p53 + fibroblasts, culture density, and size of fibroblast nuclei did not differ from the control parameters; a significant increase in the total area of nucleoli in cell nuclei was recorded. In the series with peptide G, the indicators of the proportion of p53 + fibroblasts, the size of fibroblast nuclei, the number and total area of nucleoli were similar to the control indicators, and a significant increase in the cell culture density was revealed, compared to the control. Conclusions. The results of the study indicate a direct cytoprotective effect of peptides - non-opiate analogues of leu-enkephalin, including conditions of blockade of the polyamine system.

About the Authors

E. N. Sazonova
Far Eastern State Medical University of Minzdrav of Russia; Far Eastern Scientific Center for Physiology and Pathology of Respiration – Research Institute for the Protection of Motherhood and Childhood
Russian Federation

Elena N. Sazonova - doctor of medical sciences, professor.

680000, Khabarovsk, Murav’yeva-Amurskogo st., 35; 680022, Khabarovsk, Voronezhskaya st., 49



O. G. Repa
Territorial Consultative and Diagnostic Center
Russian Federation

Olga G. Repa.

681000, Komsomolsk-na-Amure, Dimitrova st., 12



Yu. B. Malofey
Far Eastern State Medical University of Minzdrav of Russia
Russian Federation

Yuliya B. Malofey - candidate of biological sciences.

680000, Khabarovsk, Murav’yeva-Amurskogo st., 35



References

1. Sazonova E.N., Lebed’ko O.A., Pinaeva O.G., Tsimbalist N.A., Kupriyanova D.A., Tarasov P.K., Malofey Yu.B. Role of amino acid arginine and nitric oxide in mechanisms of cytoprotective effect of non-opiate leu-enkephalin analogue in vitro. Bull. Exp. Biol. Med. 2021;172(2):270–275. doi: 10.1007/s10517-021-05374-2

2. Rider J.E., Hacker A., Mackintosh C.A., Pegg A.E., Woster P.M., Casero R.A.Jr. Spermine and spermidine mediate protection against oxidative damage caused by hydrogen peroxide. Amino Acids. 2007;33(2):231–240. doi: 10.1007/s00726-007-0513-4

3. Egorov O.S., Borisova N.Yu., Borisova E.Ya., Rezhabbaev M.L., Afanas’eva E.Yu., Arzamastsev E.V. Structure and biological action of analogs and derivatives of biogenic polyamines. Tonkiye khimicheskiye tekhnologii = Fine Chemical Technologies. 2021;16(4):287–306. [In Russian]. doi: 10.32362/2410-6593-2021-16-4-287-306

4. Tong F., Liu S., Yan B., Li X., Ruan S., Yang S. Endogenous ornithine decarboxylase/polyamine system mediated the antagonist role of insulin/PEG-CMCS preconditioning against heart ischemia/reperfusion injury in diabetes mellitus. Int. J. Nanomedicine. 2018;13:2507–2520. doi: 10.2147/ijn.s160848

5. Grossi M., Phanstiel O., Rippe C., Swärd K., Alajbegovic A., Albinsson S., Forte A., Persson L., Hellstrand P., Nilsson B.O. Inhibition of polyamine uptake potentiates the anti-proliferative effect of polyamine synthesis inhibition and preserves the contractile phenotype of vascular smooth muscle cells. J. Cell. Physiol. 2016;231(6):1334–1342. doi: 10.1002/jcp.25236

6. Samokhvalov V.A., Smetanina M.D., Museykina N.Yu., Melnikov G.V., Fedotova O.V., Ignatov V.V. The influence of low doses of hydrogen peroxide on metabolism of blood cells. Biomeditsinskaya khimiya = Biomedical Chemistry. 2003;49(2):122–127. [In Russian].

7. Morphological diagnosis. Preparation of material for histological examination and electron microscopy: a guide. Ed. D.Je. Korzhevsky. Saint-Petersburg: SpetsLit, 2013. 127 p. [In Russian].

8. Lewinska A., Wnuk M., Grzelak A., Bartosz G. Nucleolus as an oxidative stress sensor in the yeast Saccharomyces cerevisiae. Redox Rep. 2010;15(2):87–96. doi: 10.1179/174329210x12650506623366

9. Sazonova E.N., Kuznetsova M.S., Lebed’ko О.А., Tsimbalist N.A., Vasileva E.A., Mishchenko N.P. Cytoprotective effect of Echinochrome A in primary culture of pulmonary fibroblasts from albino rats under conditions of oxidative stress. Bull. Exp. Biol. Med. 2020;169(4):582–585. doi: 10.1007/s10517-020-04933-3

10. Sazonova E.N., Lebed’ko O.A., Denisyuk G.A., Zhmerenetskiy K.V., Dobrykh V.A. Cytoprotective effect of non-opioid leu-enkephalin analogue in primary culture of pulmonary fibroblasts in oxidative stress. Kazanskiy meditsinskiy zhurnal = Kazan Medical Journal. 2019;100(1):153–157. [In Russian]. doi: 110.17816/KMJ2019-153

11. Yoon K.B., Park K.R., Kim S.Y., Han S.Y. Induction of nuclear enlargement and senescence by sirtuin inhibitors in glioblastoma cells. Immune Netw. 2016;16(3):183–188. doi: 10.4110/in.2016.16.3.183

12. Zou C., Vlastos A.T., Yang L., Wang J., Nishioka K., Follen M. Effects of difluoromethylornithine on growth inhibition and apoptosis in human cervical epithelial and cancerous cell lines. Gynecol. Oncol. 2002;85(2):266–273. doi: 10.1006/gyno.2002.6599

13. Grossi M., Persson L., Swärd K., Turczyńska K.M., Forte A., Hellstrand P., Nilsson B.O. Inhibition of polyamine formation antagonizes vascular smooth muscle cell proliferation and preserves the contractile phenotype. Basic Clin. Pharmacol. Toxicol. 2014;115(5):379–388. doi: 10.1111/bcpt.12237

14. Brooks W.H. Viral impact in autoimmune diseases: expanding the “X Chromosome-Nucleolus Nexus” hypothesis. Front. Immunol. 2017;8:1657. doi: 10.3389/fimmu.2017.01657

15. Shim H.W., Moon M.S., Shin K.S., Cho H.J., Yoo B.S., Kim I.G. Alpha-difluoromethylornithine, ornithine decarboxylase inhibitor, antagonizes H2O2-induced cytotoxicity in HL-60 leukemia cells: regulation of iron-dependent lysosomal damage. Cell. Biol. Toxicol. 2003;19(6):393–405. doi: 10.1023/b:cbto.0000013355.63593.35


Review

For citations:


Sazonova E.N., Repa O.G., Malofey Yu.B. Cytoprotective effect of non-opiate leu-enkephalin analogues against the background of ornithine decarboxylase inhibitor exposure. Сибирский научный медицинский журнал. 2024;44(6):155-161. (In Russ.) https://doi.org/10.18699/SSMJ20240615

Views: 679


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


ISSN 2410-2512 (Print)
ISSN 2410-2520 (Online)