Changes in the liver of Djungarian hamsters under conditions of a three-month supply of water-soluble silicon of various concentrations



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Abstract

Relevance. Silicon enters the human body through drinking water, air and food. Silicon nanoparticles used in the cosmetic, pharmaceutical and food industries are known to have biological activity. Taking into account the widespread prevalence of silicon compounds, the issue of the safety of its use is becoming more urgent.

Aim. To study the effect of water-soluble silicon on the morphological structure of the liver of Djungarian hamsters for three months.

Materials and methods. The experiment was carried out on Djungarian hamsters kept in normal vivarium conditions under natural light. The animals were divided into three groups: control, which received bottled drinking water; the first experimental group, which received the same water, but with the addition of sodium metasilicate nine-hydrate at a concentration of 10 mg/l in terms of silicon; the second experimental group, which also received the same water, but with the concentration of sodium metasilicate nine-hydrate doubled (up to 20 mg/l). After three months, the animals were removed from the experiment. Sections were processed by general histological (hematoxylin and eosin, Van Gieson method, toluidine blue), histochemical (MAO-positive cells) methods.

Results. In the liver of hamsters from the experimental groups, changes in the micromorphological structure were revealed, such as an increase in the nuclear area, nuclear-cytoplasmic ratio of hepatocytes, and the diameter of sinusoidal capillaries. Moreover, more pronounced changes were observed in the liver of hamsters of the second experimental group, such as polymorphic cell infiltration of the portal tracts, an increase in the number of eosinophils, deformation of hepatocyte nuclei and the appearance of apoptotic bodies. A decrease in the area of mast cells and an increase in their number, as well as the number of MAO-positive cells in the liver of hamsters of both experimental groups were recorded.

Conclusion. An increase in the concentration of silicon supplied with drinking water in both cases is reflected in the micromorphological structure of the liver of hamsters. Moreover these changes are more pronounced in the liver of hamsters of the second experimental group.

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About the authors

Evgeniia A. Grigoreva

IN Ulyanov Chuvash State University

Author for correspondence.
Email: shgrev@yandex.ru
ORCID iD: 0000-0003-3626-2750
SPIN-code: 9971-5435

assistant of the department of medical biology with a course of microbiology and virology

Russian Federation, 428015, Chuvash Republic, Cheboksary, Moskovsky Prospect, 15

Valentina S. Gordova

Immanuel Kant Baltic Federal University

Email: crataegi@rambler.ru
ORCID iD: 0000-0001-5109-9862
SPIN-code: 2527-1634

Cand. Sci. (Med.), Associate Professor, Department of Fundamental Medicine of the Medical Institute

Russian Federation, 236041, Russia, Kaliningrad, st. A. Nevsky, 14

Valentina E. Sergeeva

IN Ulyanov Chuvash State University

Email: kafedra-biology@yandex.ru
ORCID iD: 0000-0003-3471-5226
SPIN-code: 9827-3454

Dr. Sci. Biol., Professor, Department of Medical Biology with a course of Microbiology and Virology

Russian Federation, 428015, Chuvash Republic, Cheboksary, Moskovsky Prospect, 15

Roman D. Mikheikin

IN Ulyanov Chuvash State University

Email: mikheykin2002@mail.ru
ORCID iD: 0009-0002-6731-7224

4rd year Student, Medicine Faculty

Russian Federation, 428015, Chuvash Republic, Cheboksary, Moskovsky Prospect, 15

Valeriia S. Dedikina

IN Ulyanov Chuvash State University

Email: valary0d@gmail.com
ORCID iD: 0009-0005-5045-4291

6th year Student, Medicine Faculty

Russian Federation, 428015, Chuvash Republic, Cheboksary, Moskovsky Prospect, 15

Darya A. Braun

Immanuel Kant Baltic Federal University

Email: dashabraun1612@gmail.com
ORCID iD: 0009-0001-1809-1161

5th year Student, Graduate School of Medicine

Russian Federation, 236041, Russia, Kaliningrad, st. A. Nevsky, 14

References

  1. Martin KR. Silicon: the health benefits of a metalloid. Metal Ions in life Science. 2013; 13:451–473. doi: 10.1007/978-94-007-7500-8_14.
  2. Martin KR. The chemistry of silica and its potential health benefits. Journal of Nutrition, Health and Aging. 2007;11(2):94–97.
  3. Athinarayanan J, Alshatwi AA, Periasamy VS, Al-Warthan AA. Identification of nanoscale ingredients in commercial food products and their induction of mitochondrially mediated cytotoxic effects on human mesenchymal stem cells. Journal of Food Science. 2015;80(2):459–464. doi: 10.1111/1750-3841.12760.
  4. Lotfipour F, Shahi S, Farjami A, Salatin S. et al. Safety and toxicity issues of therapeutically used nanoparticles from the oral route. BioMed Research International. 2021;2021:e9322282. doi: 10.1155/2021/9322282.
  5. Martin KR. Dietary Silicon: Is. Biofortification Essential? Journal of nutrition and food science forecast. 2018:1(2):1006.
  6. Jugdaohsingh R, Anderson SHC, Tucker KL, Elliott H. et al. Dietary silicon intake and absorption. American Society for Clinical Nutrition. 2002;75:887–893. doi: 10.1093/ajcn/75.5.887
  7. Kamenetskaya DB. Silicon, Its Forms and Methods of Determination in Water Bodies: A Review. Public Health and Life Environment – PH&LE. 2022;(6):15-22. (In Russ.). doi: 10.35627/2219-5238/2022-30-6-15-22.
  8. Firouzamandi M, Hejazy M, Mohammadi A. et al. In Vivo Toxicity of Oral Administrated Nano-SiO2: Can Food Additives Increase Apoptosis? Biological trace element research. 2023;201(10):4769–4778. doi: 10.1007/s12011-022-03542-7.
  9. Joshi D., Keane D., Brind E. Hepatology at a Glance. Moscow: GEOTAR-Media, 2018. (In Russ.).
  10. Myadelets OD, Lebedeva EI. Funktsional'naya morfologiya i elementy obshchei patologii pecheni : monografiya. Vitebsk : VGMU, 2018. (In Russ.).
  11. Zaitseva NV, Zemlyanova MA, Zvezdin VN et al. Influence of silicon dioxide nanoparticles on the morphology of internal organs in rats after oral administration. Health risk analysis. 2016;4:80–94. (In Russ.). doi: 10.21668/health.risk/2016.4.10.
  12. Yukina GYu, Sukhorukova EG, Polovnikov IV, Kryzhanovskaya EA. Effect of Silicon Dioxide Nanoparticles on Liver Morphology of Rats in Parenteral Administration. Journal of Anatomy and Histopathology. 2021;10(4):85–88. (In Russ.) doi: 10.18499/2225-7357-2021-10-4-85-88.
  13. Tassinari R, Martinelli A, Valeri M. et al. Amorphous silica nanoparticles induced spleen and liver toxicity after acute intravenous exposure in male and female rats. Toxicology and Industrial Health. 2021;37(6):328–335. doi: 10.1177/07482337211010579.
  14. Azouz RA, Korany RMS. Toxic Impacts of Amorphous Silica Nanoparticles on Liver and Kidney of Male Adult Rats: an In Vivo Study. Biological trace element research. 2021;199(7):2653–2662. doi: 10.1007/s12011-020-02386-3.
  15. Liang Q, Sun M, Ma Y. et al. Adverse effects and underlying mechanism of amorphous silica nanoparticles in liver. Chemosphere. 2023;311(Pt 1):136955. doi: 10.1016/j.chemosphere.2022.136955.
  16. Badawy MM, Sayed-Ahmed MZ, Almoshari Y. et al. Magnesium Supplementation Alleviates the Toxic Effects of Silica Nanoparticles on the Kidneys, Liver, and Adrenal Glands in Rats. Toxics. 2023;11(4):381. doi: 10.3390/toxics11040381.
  17. Mahmoud AM, Desouky EM, Hozayen WG. et al. Mesoporous silica nanoparticles trigger liver and kidney Injury and fibrosis via altering TLR4/NF-κB, JAK2/STAT3 and Nrf2/HO-1 signaling in rats. Biomolecules. 2019;9(10):528. doi: 10.3390/biom9100528.
  18. Sun M. Zhang J, Liang S. et al. Metabolomic characteristics of hepatotoxicity in rats induced by silica nanoparticles. Ecotoxicology and environmental safety. 2021;208:111496. doi: 10.1016/j.ecoenv.2020.111496.
  19. Sadek SA, Soliman AM, Marzouk M. Ameliorative effect of Allolobophora caliginosa extract on hepatotoxicity induced by silicon dioxide nanoparticles. Toxicology and Industrial Health. 2016;32(8):1358–1372. doi: 10.1177/0748233714561075.
  20. Yu Y, Duan J, Li Y, Li Y. et al. Silica nanoparticles induce liver fibrosis via TGF-β1/Smad3 pathway in ICR mice. International Journal of Nanomedicine. 2017;12:6045–6057. doi: 10.2147/IJN.S132304.
  21. Grigor'eva EA. Morphological features of the liver when exposed to a water-soluble silicon compound. Medical academic journal. 2016; 16(4): 71–72. (In Russ).
  22. Grigor'eva EA, Dedikina VS, Mikheikin RD et al. Comprehensive assessment of morphological changes in the liver of rabbits exposed to water-soluble silicon for three months. Acta Medica Eurasica. 2023;3:84–93. (In Russ). doi: 10.47026/2413-4864-2023-3-84-93.
  23. Smitha T, Sharada P, Girish H. Morphometry of the basal cell layer of oral leukoplakia and oral squamous cell carcinoma using computer-aided image analysis. Journal of Oral and Maxillofacial Pathology. 2011;15(1):26–33. doi: 10.4103/0973-029X.80034.
  24. Il'ina LYu., Sapozhnikov SP, Kozlov VA et al. Quantitative evaluation of mast cells sulfation. Acta medica Eurasica. 2020;2:43–53.
  25. Pustyl'nyak VO, Kirulli V, Dzhervazi PD et al. Effect of triphenyldioxane on phase I xenobiotic metabolism enzymes in the liver of rats and rabbits. Bulletin of Experimental Biology and Medicine. 2006;141(6):646–648. doi: 10.1007/s10517-006-0256-3.
  26. Ardies CM, Lasker JM, Lieber CS. Characterization of the cytochrome P-450 monooxygenase system of hamster liver microsomes. Effects of prior treatment with ethanol and other xenobiotics. Biochemical Pharmacology.1987;36(21):3613–3619. doi: 10.1016/0006-2952(87)90010-4.
  27. Bhadoria P, Nagar M, Bharihoke V, Bhadoria AS. Ethephon, an organophosphorous, a Fruit and Vegetable Ripener: Has potential hepatotoxic effects? Journal of family medicine and primary care. 2018;7(1):179–183. doi: 10.4103/jfmpc.jfmpc_422_16.
  28. Hussein WF, Farahat FY, Abass MA, Shehata AS. Hepatotoxic potential of gibberellic acid (GA3) in adult male albino rats. Life Sciences Journal. 2011;8:373–83.
  29. Yukina GYu., Zhuravskii SG, Panevin AA., Galagudza MM, Tomson VV, Blum NM. Macrophage granulomas and mast cells as beginning organ remodeling in case of silicone dioxide nanoparticles chronic toxicity. Translational Medicine. 2016;3(2):70-79. (In Russ.). doi: 10.18705/2311-4495-2016-3-2-70-79.
  30. Xu L, Yang Y, Wen Y, Jeong JM et al. Hepatic recruitment of eosinophils and their protective function during acute liver injury. Journal of Hepatology. 2022;77(2):344–352. doi: 10.1016/j.jhep.2022.02.024.
  31. Kondrashevskaya MV. Mast Cells Heparin — New Information on the Old Component (Review). Annals of the Russian Academy of Medical Sciences. 2021;76(2):149–158. (In Russ.). doi: https://doi.org/10.15690/vramn1284.
  32. Yurina NA, Radostina AI. Mast cells and their role in the body: textbook. Peoples’ Friendship University named after. Patrice Lumumba. Department of histology and embryology. Moscow: [b. i.], 1977. (In Russ.).
  33. Gusel'nikova VV, Pronina AP, Nazarov PG, Polevshchikov AV. Origin of mast cells: current state of the problem. Collection of works dedicated to the 80-th anniversary Alekseya Andreevicha Klishova. Issue 2. Saint Petersburg : DEAN, 2010. P. 108-115. (In Russ.).
  34. Gorbunova AV. Brain content of biogenic amines and stabilityof cardio-vascular reaction under emotional stress. The Russian Journal of Neuroscience. 2006;1:3–19. (In Russ.).
  35. Mayanskii AN, Pazyuk EA, Makarova TP, Parshakova RA, Pikuza OI. Mechanism and diagnostic capabilities of the reaction of reduction of nitroblue tetrazolium by human neutrophils. Kazan Medical Journal. 1981;4:64–68. (In Russ.).

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