Preview

Medicine and ecology

Advanced search

STATE OF BLOOD HOMEOSTASIS IN FEMALE RATS UNDER ISOLATED AND COMBINED EXPOSURE TO HEXAVALENT CHROMIUM AND GAMMA RADIATION

https://doi.org/10.59598/ME-2305-6053-2025-116-3-99-107

Abstract

Aim. Study of the state of blood homeostasis in female rats under isolated and combined exposure to hexavalent chromium and gamma radiation.

Materials and methods. The experiment included groups of rats exposed to gamma radiation, as well as combined exposure to gamma radiation and chromium. In the acute phase, peripheral blood parameters, markers of oxidative stress (MDA, SOD, CAT) and cytokine status (IL-1-beta, IL-6, IL-10, TNF-α) were evaluated.

Results and discussion. Gamma radiation significantly reduced antioxidant protection (SOD, CAT) and caused severe inflammation (increased the level of IL-1-beta). These changes were statistically significant, and the high correlation between the groups confirmed the reliability of the results. The mechanisms of induced mutagenesis under combined exposure are associated with increased free radical oxidation and depletion of the antioxidant system.

Conclusions. Combined exposure to hexavalent chromium and gamma radiation causes more severe homeostasis disorders compared to isolated use. The data suggest the need to develop chemoprophylaxis methods to reduce cancer risks, especially in cases where carcinogens have a combined effect.

About the Authors

M. K. Iztleuov
Department of Natural Sciences, West Kazakhstan Medical University named after Marat Ospanov NC JSC
Kazakhstan

030000, Aktobe c., Maresyeva str., 68



Ye. M. Iztleuov
Department of Radiology, West Kazakhstan Medical University named after Marat Ospanov NC JSC
Kazakhstan

030000, Aktobe c., Maresyeva str., 68



References

1. Abrahao R., Ribeiro R.C., Brunson A., Keegan T.H. The burden of second primary cancers among childhood cancer survivors. Ann. Cancer Epidem. 2020; 4: 7. https://doi.org/10.21037/ace-2020-01

2. Keikhaei B., Bahadoram M., Keikha A., Bahadoram S., Hassanzadeh S., Mahmoudian-Sani M.R. Late side effects of cancer treatment in childhood cancer survivors. J. Oncol. Pharm. Pract. 2023; 29 (4): 885-892. https://doi.org/10.1177/10781552221087611

3. Meistrich M. L. Effects of chemotherapy and radiotherapy on spermatogenesis in humans. Fertil. Steril. 2013; 100 (5): 1180-1186. https://doi.org/10.1016/j.fertnstert.2013.08.010

4. Long-term Side Effects of Cancer. American Cancer Society. https://www.cancer.net/survivorship/longterm-side-effects-cancer-treatment

5. Choi D.K., Helenowski I., Hijiya N. Secondary malignancies in pediatric cancer survivors: perspectives and review of the literature. Int. J. Cancer. 2014; 135 (8): 1764-1773. https://doi.org/10.1002/ijc.28991

6. Friedman D.L., Whitton J., Leisenring W., Mertens A.C., Hammond S., Stovall M., Donaldson S.S., Meadows AT., Robison L.L., Neglia J.P. Subsequent neoplasms in 5-year survivors of childhood cancer: the Childhood Cancer Survivor Study. J. Natl. Cancer Inst. 2010; 102 (14): 1083-1095. https://doi.org/10.1093/jnci/djq238

7. Linet M.S., Kazzi Z., Paulson J.A., COUNCIL ON ENVIRONMENTAL HEALTH. Pediatric Considerations Before, During, and After Radiological or Nuclear Emergencies. Pediatrics. 2018; 142 (6): e20183001. https://doi.org/10.1542/peds.2018-3001

8. Demina Je.A., Kljushin D.A., Petunin Ju.I., Pilinskaja M.A. Radiacionnaja citogenetika: Russko-anglijskij slovar'-spravochnik. K.: Zdorov'ja; 2009: 368.

9. Sun L., Wang X., Yao H., Li W., Son Y.O., Luo J., Liu J., Zhang Z. Reactive oxygen species mediate Cr (VI)-induced S phase arrest through p53 in human colon cancer cells. J. Environ. Pathol. Toxicol. Oncol. 2012; 31 (2): 95-107. https://doi.org/10.1615/jenvironpatholtoxicoloncol.v31.i2.20

10. Seidler A., Jähnichen S., Hegewald J., Fishta A., Krug O., Rüter L., Strik C., Hallier E., Straube S. Systematic review and quantification of respiratory cancer risk for occupational exposure to hexavalent chromium. Int. Arch. Occup. Environ. Health. 2013; 86 (8): 943-55. https://doi.org/10.1007/s00420-012-0822-0

11. Thompson C.M., Kirman C.R., Proctor D.M., Haws L.C., Suh M., Hays S.M., Hixon J.G., Harris M.A. A chronic oral reference dose for hexavalent chromium-induced intestinal cancer. J. Appl. Toxicol. 2014; 34 (5): 525-536. https://doi.org/10.1002/jat.2907

12. Valko M., Morris H., Cronin M.T. Metals, toxicity and oxidative stress. Curr. Med. Chem. 2005; 12 (10): 1161-1208. https://doi.org/10.2174/0929867053764635

13. Reynolds M., Stoddard L., Bespalov I., Zhitkovich A. Ascorbate acts as a highly potent inducer of chromate mutagenesis and clastogenesis: linkage to DNA breaks in G2 phase by mismatch repair. Nucleic. Acids Res. 2007; 35 (2): 465-476. https://doi.org/10.1093/nar/gkl1069

14. Minaev Ju.L., Supil'nikov A.A., Zarubina E.G., Istratov P.A. Vlijanie malyh doz gamma-izluchenija na organizm cheloveka. Reabilitacija, Vrach i Zdorov'e. 2023; 13 (1): 64-70. https://doi.org/10.20340/vmi-rvz.2023.1.CLIN.7

15. Vorobcova I.E. Transgeneracionnaja peredacha radiacionno-inducirovannoj nestabil'nosti genoma i predraspolozhennosti k kancerogenezu. Voprosy onkologii. 2008; 4 (54): 490-493.

16. Little M.P, Goodhead D.T, Bridges B.A, Bouffler S.D. Evidence relevant to untargeted and transgenerational effects in the offspring of irradiated parents. Mutat. Res. 2013; 753 (1): 50-67. https://doi.org/10.1016/j.mrrev.2013.04.001

17. Vorobcova I.E., Kanaeva M.D., Semenov A.V., Dobrogorskaja M.V. Vozrast roditelej pri zachatii i risk kancerogeneza u detej. Voprosy onkologii. 2018; 1 (64).: 41-47.

18. Nomura T., Baleva L.S., Ryo H., Adachi S., Sipyagina A.E., Karakhan N.M. Transgenerational Effects of Radiation on Cancer and Other Disorders in Mice and Humans. J. Radiat. Cancer Res. 2017; 8 (3): 123-134.

19. Iztleuov M.K., Iztleuov E.M. Hrom men bor қosylystarynyң bіrlesken әserіnen indukcijalanғan reproduktivtіk funkcija bұzylystaryn baғalau zhәne korrekcijalau. Әdіstemelіk nұsқau. Aқtөbe; 2022: 34.

20. Andrews D., Walker B. «Erin Brockovich»Carcinogen in Tap Water of More than 200 Million Americans. Washington, D.C.; 2016: 13.

21. Dubey R, Verma P, Kumar S. Cr (III) genotoxicity and oxidative stress: An occupational health risk for leather tannery workers of South Asian developing countries. Toxicology and Industrial Health. 2022; 38 (2): 112-126. doi:10.1177/07482337211055131

22. Gaziev A.I. Nizkaja jeffektivnost' reparacii kriticheskih povrezhdenij DNK, vyzyvaemyh malymi dozami radiacii. Radiacionnaja biologija. Radiojekologija. 2011; 51 (5): 512-529.

23. Zhizhina G.P. Vlijanie malyh doz nizkointensivnoj ionizirujushhej radiacii na strukturu i funkcii DNK. Radiacionnaja biologija. Radiojekologija. 2011; 51 (2): 218-228.

24. Bashlykova L.A. Nasledovanie citogeneticheskih i molekuljarno-kletochnyh jeffektov v kletkah kostnogo mozga zhivotnyh pri hronicheskom vozdejstvii ionizirujushhego izluchenija. Izvestija Samarskogo nauchnogo centra RAN. 2017; 19 (2-3): 420-425.

25. Baleva L.S., Sipjagina A.E. Prediktory riska formirovanija radiacionno-inducirovannyh stohastich- M. K. Iztleuov1, Ye. M. Iztleuov2* eskih zabolevanij v pokolenijah detej iz semej obluchennyh roditelej – aktual'naja problema sovremennosti. Rossijskij vestnik perinatologii i pediatrii. 2019; 64 (1): 7-14. https://doi.org/10.21508/1027-4065-2019-64-17-14


Review

For citations:


Iztleuov M.K., Iztleuov Ye.M. STATE OF BLOOD HOMEOSTASIS IN FEMALE RATS UNDER ISOLATED AND COMBINED EXPOSURE TO HEXAVALENT CHROMIUM AND GAMMA RADIATION. Medicine and ecology. 2025;(3):99-107. (In Russ.) https://doi.org/10.59598/ME-2305-6053-2025-116-3-99-107

Views: 6


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


ISSN 2305-6045 (Print)
ISSN 2305-6053 (Online)