Morphofunctional changes in the tissue of the brain, liver and kidneys of white rats under the influence of selenium nanocomposite encapsulated in the polymer matrix of arabinogalactan
https://doi.org/10.29413/ABS.2021-6.5.9
Abstract
Introduction. Due to their high biocompatibility, substances based on nanosized selenium particles, encapsulated in natural or synthetic polymer matrices, are promising materials for the creation of biomedical preparations of diagnostic and therapeutic value. Selenium nanoparticles are successfully used in the diagnosis of various types of cancer. In addition to the diagnostic value, selenium nanoparticles have their own prophylactic and oncological effect. This paper presents the results of a study of the toxicity of the Se nanocomposite encapsulated in the polymer matrix of arabinogalactan (SeAG). The emergence and development of the pathological process in the tissue of the brain, liver and kidneys during subacute administration of this nanocomposite was studied.
Materials and methods. Twenty white outbred male rats weighing 200–220 g were used in the work. Animals were orally administered a solution of the selenium nanocomposite at a dose of 500 μg per kilogram of animal body weight for 10 days. Then, using the methods of histological analysis, the severity of the biological response of the organism to the introduction of this nanocomposite was assessed. An analysis of the state of the tissue of the liver, kidneys and the sensorimotor cortex of the brain was carried out.
Results. With the intragastric administration of this drug, there is stasis of blood in the portal tracts, a pronounced macrophage reaction and diapedesis of leukocytes in the liver tissue. There is a decrease in the number of normal neurons per unit area, a decrease in the number of astroglia cells and an increase in the number of degeneratively altered neurons in the tissue of the sensorimotor cortex. There is also an increase in connective tissue in the cortex of the kidney, with the formation of fibrosis and a decrease in the area of the Shumlyansky – Bowman capsule.
Conclusion. The effect of the investigated nanocomposite is characterized by the development of a pronounced pathological process in the central nervous and hepatorenal systems of the body.
About the Authors
E. A. TitovRussian Federation
Cand. Sc. (Biol.), Senior Research Officer at the Laboratory of Biomodeling and Translational Medicine,
12a mikrorayon 3, Angarsk 665827
V. S. Rukavishnikov
Russian Federation
Corresponding Member of RAS, Chief Research Officer,
12a mikrorayon 3, Angarsk 665827
L. M. Sosedova
Russian Federation
Dr. Sc. (Med.), Leading Research Officer, Head of the Laboratory of Biomodeling and Translational Medicine,
12a mikrorayon 3, Angarsk 665827
M. A. Novikov
Russian Federation
Cand. Sc. (Biol.), Senior Research Officer at the Laboratory of Biomodelling and Translational Medicine,
12a mikrorayon 3, Angarsk 665827
E. V. Buynova
Russian Federation
Research Assistant at the Laboratory of Biomodelling and Translational Medicine,
12a mikrorayon 3, Angarsk 665827
References
1. Maiyo F, Singh M. Selenium nanoparticles: potential in cancer gene and drug delivery. Nanomedicine (Lond). 2017; 12(9): 1075-1089. doi: 10.2217/nnm-2017-0024
2. Hosnedlova B, Kepinska M, Skalickova S, Fernandez C, Ruttkay-Nedecky B, Peng Q, et al. Nano-selenium and its nanomedicine applications: A critical review. Int J Nanomedicine. 2018; 13: 2107-2128. doi: 10.2147/IJN.S157541
3. Shurygina IA, Shurygin MG. Selenium nanocomposites – prospects for application in oncology. Journal of new medical technologies. 2020; 1: 81-86. (In Russ.). doi: 10.20333/2500136-2018-4-31-37
4. Huang J, Huang W, Zhang Z, Lin X, Lin H, Peng L, et al. Highly uniform synthesis of selenium nanoparticles with EGFR targeting and tumor microenvironment-responsive ability for simultaneous diagnosis and therapy of nasopharyngeal carcinoma. ACS Appl Mater Interfaces. 2019; 11(12): 11177-11193. doi: 10.1021/acsami.8b22678
5. Zhao Y, Sun Q, Zhang X, Baeyens J, Su H. Selfassembled selenium nanoparticles and their application in the rapid diagnostic detection of small cell lung cancer biomarkers. Soft Matter. 2018; 14(4): 481-489. doi: 10.1039/c7sm01687e
6. Trukhan IS, Dremina NN, Lozovskaya EA, Shurygina IA. Evaluation of potential cytotoxicity in the framework of intravital observation on Biostation CT. Acta biomedica scientifica. 2018; 3(6): 48-53. (In Russ.). doi: 10.29413/ABS.2018-3.6.6
7. Wadhwani SA, Gorain M, Banerjee P, Shedbalkar UU, Singh R, Kundu GC, et al. Green synthesis of selenium nanoparticles using Acinetobacter sp. SW30: Optimization, characterization and its anticancer activity in breast cancer cells. Int J Nanomedicine. 2017; 12: 6841-6855. doi: 10.2147/IJN.S139212
8. Sonkusre P, Nanduri R, Gupta P, Cameotra SS. Improved extraction of intracellular biogenic selenium nanoparticles and their specificity for cancer chemoprevention. J Nanomed Nanotechnol. 2014; 5(2): 94-105. doi: 10.4172/2157-7439.1000194
9. El-Bayoumy K. The protective role of selenium on genetic damage and on cancer. Mutat Res. 2001; 475(1-2): 123-139. doi: 10.1016/s0027-5107(01)00075-6
10. Zeng H, Combs GF. Selenium as an anticancer nutrient: Roles in cell proliferation and tumor cell invasion. J Nutr Biochem. 2008; 19(1): 1-7. doi: 10.1016/j.jnutbio.2007.02.005
11. Zeng D, Zhao J, Luk KH, Cheung S.T, Wong KH, Chen T. Potentiation of in vivo anticancer efficacy of selenium nanoparticles by mushroom polysaccharides surface decoration. J Agric Food Chem. 2019; 67(10): 2865-2876. doi: 10.1021/acs.jafc.9b00193
12. Huang G, Liu Z, He L, Luk KH, Cheung ST, Wong KH, et al. Autophagy is an important action mode for functionalized selenium nanoparticles to exhibit anticolorectal cancer activity. Biomater Sci. 2018; 6(9): 2508-2517. doi: 10.1039/c8bm00670a
13. Ganther HE. Selenium metabolism, selenoproteins and mechanisms of cancer prevention: complexities with thioredoxin reductase. Carcinogenesis. 1999; 20(9): 1657-1666. doi: 10.1093/carcin/20.9.1657
14. Xia Y, Chen Y, Hua L, Zhao M, Xu T, Wang C, et al. Functionalized selenium nanoparticles for targeted delivery of doxorubicin to improve non-small-cell lung cancer therapy. Int J Nanomedicine. 2018; 13: 6929-6939. doi: 10.2147/IJN.S174909
15. Chen T, Wong YS, Zheng W, Bai Y., Huang L. Selenium nanoparticles fabricated in Undaria pinnatifida polysaccharide solutions induce mitochondria-mediated apoptosis in A375 human melanoma cells. Colloids Surf B: Biointerfaces. 2008; 67(1): 26-31. doi: 10.1016/j.colsurfb.2008.07.010
16. Titov EA, Sosedova LM, Novikov MA. Alteration of white rat brain tissue induced by exposure to silver nanocomposite encapsulated on a polymer matrix. Pathological physiology and experimental therapy. 2015; 59(4): 41-46. (In Russ.).
17. Korzhevsky DE. A brief summary of the basics of histological techniques for physicians and laboratory assistants-histologists. Saint Petersburg: Krof; 2005. (In Russ.).
18. Bogolepov NN, Koplik EV, Krivitskaya GN, Popova EN, Sudakov KV. Structural and functional characteristics of neurons in the sensorimotor cortex of the brain in rats with different resistance to emotional stress. Bulletin of Experimental Biology and Medicine. 2001; 132(8): 124-128. (In Russ.).
19. Naderi M, Puar P, Zonouzi-Marand M, Chivers DP, Niyogi S, Kwong R. A comprehensive review on the neuropathophysiology of selenium. Sci Total Environ. 2021; 767: 144329. doi: 10.1016/j.scitotenv.2020.144329
20. Powers M, Liu L, Deemer D, Chen S, Scholl A, Yoshinaga M, et al. Selenite inhibits notch signaling in cells and mice. Int J Mol Sci. 2021; 22(5): 2518. doi: 10.3390/ijms22052518
21. Pinto-Vidal F, Carvalho CDS, Abdalla FC, Ceschi-Bertoli L, Moraes Utsunomiya HS, Henrique da Silva R, et al. Metabolic, immunologic, and histopathologic responses on premetamorphic American bullfrog (Lithobates catesbeianus) following exposure to lithium and selenium. Environ Pollut. 2021; 270: 116086. doi: 10.1016/j.envpol.2020.116086
22. Hassan I, Ebaid H, Al-Tamimi J, Habila MA, Alhazza IM, Rady AM. Selenium nanoparticles mitigate diabetic nephropathy and pancreatopathy in rat offspring via inhibition of oxidative stress. J King Saud Univ Sci. 2021; 33(1): 101265. doi: 10.1016/j.jksus.2020.101265
23. Levitskaya ES. Mechanisms of renal fibrosis formation taking into account microvascular lesions. Medicinskij vestnik Yuga Rossii. 2017; 8(1): 21-27. (In Russ.). doi: 10.21886/2219-8075-2017-1-21-27
Review
For citations:
Titov E.A., Rukavishnikov V.S., Sosedova L.M., Novikov M.A., Buynova E.V. Morphofunctional changes in the tissue of the brain, liver and kidneys of white rats under the influence of selenium nanocomposite encapsulated in the polymer matrix of arabinogalactan. Acta Biomedica Scientifica. 2021;6(5):92-99. (In Russ.) https://doi.org/10.29413/ABS.2021-6.5.9