Changes in the liver of Djungarian hamsters under conditions of a three-month supply of water-soluble silicon of various concentrations
- Authors: Grigoreva E.A.1, Gordova V.S.2, Sergeeva V.E.1, Mikheikin R.D.1, Dedikina V.S.1, Braun D.A.2
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Affiliations:
- I.N. Ulyanov Chuvash State University
- Immanuel Kant Baltic Federal University
- Issue: Vol 24, No 1 (2024)
- Pages: 97-106
- Section: Original research
- Published: 11.09.2024
- URL: https://journals.eco-vector.com/MAJ/article/view/625800
- DOI: https://doi.org/10.17816/MAJ625800
- ID: 625800
Cite item
Abstract
BACKGROUND: 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 (monoamine oxidase-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 monoamine oxidase-positive cells in the liver of hamsters of both experimental groups were recorded.
CONCLUSIONS: 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
I.N. Ulyanov Chuvash State University
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, 15 Moskovsky Ave., Cheboksary, 428015, Chuvash RepublicValentina S. Gordova
Immanuel Kant Baltic Federal University
Email: crataegi@rambler.ru
ORCID iD: 0000-0001-5109-9862
SPIN-code: 2527-1634
MD, Cand. Sci. (Medicine), Assistante Professor, Department of Fundamental Medicine of the Higher School of Medicine of Institute of Medicine and Life Sciences
Russian Federation, 236041, Kaliningrad, st. A. Nevsky, 14Valentina E. Sergeeva
I.N. Ulyanov Chuvash State University
Email: kafedra-biology@yandex.ru
ORCID iD: 0000-0003-3471-5226
SPIN-code: 9827-3454
Dr. Sci. (Biology), Professor, Department of Medical Biology with a course of Microbiology and Virology
Russian Federation, 15 Moskovsky Ave., Cheboksary, 428015, Chuvash RepublicRoman D. Mikheikin
I.N. Ulyanov Chuvash State University
Email: mikheykin2002@mail.ru
ORCID iD: 0009-0002-6731-7224
4rd year Student, Medicine Faculty
Russian Federation, 15 Moskovsky Ave., Cheboksary, 428015, Chuvash RepublicValeriia S. Dedikina
I.N. Ulyanov Chuvash State University
Email: valary0d@gmail.com
ORCID iD: 0009-0005-5045-4291
6th year Student, Medicine Faculty
Russian Federation, 15 Moskovsky Ave., Cheboksary, 428015, Chuvash RepublicDarya A. Braun
Immanuel Kant Baltic Federal University
Author for correspondence.
Email: dashabraun1612@gmail.com
ORCID iD: 0009-0001-1809-1161
5th year Student, Graduate School of Medicine
Russian Federation, 236041, Kaliningrad, st. A. Nevsky, 14References
- Martin KR. Silicon: the health benefits of a metalloid. Met Ions life Sci. 2013;13:451–473. doi: 10.1007/978-94-007-7500-8_14
- Martin KR. The chemistry of silica and its potential health benefits. J Nutr Health Aging. 2007;11(2):94–97.
- 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. J Food Sci. 2015;80(2):459–464. doi: 10.1111/1750-3841.12760
- Lotfipour F, Shahi S, Farjami A, et al. Safety and toxicity issues of therapeutically used nanoparticles from the oral route. Biomed Res Int. 2021;2021:e9322282. doi: 10.1155/2021/9322282
- Martin KR. Dietary Silicon: Is Biofortification Essential? J Nutr Food Sci Forecast. 2018;1(2):1006.
- Jugdaohsingh R, Anderson SHC, Tucker KL, et al. Dietary silicon intake and absorption. Am J Clin Nutr. 2002;75:887–893. doi: 10.1093/ajcn/75.5.887
- 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. EDN: IGIDQG doi: 10.35627/2219-5238/2022-30-6-15-22
- Firouzamandi M, Hejazy M, Mohammadi A, et al. In vivo toxicity of oral administrated nano-SiO2: Can food additives increase apoptosis? Biol Trace Elem Res. 2023;201(10):4769–4778. doi: 10.1007/s12011-022-03542-7
- Joshi D, Keane D, Brind E. Visual hepatology: textbook. Transl. from English Yu.O. Shulpekova. Ed. by Ch.S. Pavlov. Moscow: GEOTAR-Media; 2018. 168 p. (In Russ.)
- Myadelets OD, Lebedeva EI. Functional morphology and elements of general liver pathology. Vitebsk: VGMU; 2018. 339 p. (In Russ.) EDN: YXKBZJ
- 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;4:74–87. EDN: XHTTDD doi: 10.21668/health.risk/2016.4.10
- 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. EDN: GLZFDO doi: 10.18499/2225-7357-2021-10-4-85-88.
- Tassinari R, Martinelli A, Valeri M, Maranghi F. Amorphous silica nanoparticles induced spleen and liver toxicity after acute intravenous exposure in male and female rats. Toxicol Ind Health. 2021;37(6):328–335. doi: 10.1177/07482337211010579
- Azouz RA, Korany RMS. Toxic impacts of amorphous silica nanoparticles on liver and kidney of male adult rats: an in vivo study. Biol Trace Elem Res. 2021;199(7):2653–2662. doi: 10.1007/s12011-020-02386-3
- 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
- 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
- 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
- Sun M, Zhang J, Liang S, et al. Metabolomic characteristics of hepatotoxicity in rats induced by silica nanoparticles. Ecotoxicol Environ Saf. 2021;208:111496. doi: 10.1016/j.ecoenv.2020.111496
- Sadek SA, Soliman AM, Marzouk M. Ameliorative effect of Allolobophora caliginosa extract on hepatotoxicity induced by silicon dioxide nanoparticles. Toxicol Ind Health. 2016;32(8):1358–1372. doi: 10.1177/0748233714561075
- Yu Y, Duan J, Li Y, et al. Silica nanoparticles induce liver fibrosis via TGF-β1/Smad3 pathway in ICR mice. Int J Nanomedicine. 2017;12:6045–6057. doi: 10.2147/IJN.S132304
- 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.) EDN: XWQLFH doi: 10.17816/MAJ16471-72
- 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. doi: 10.47026/2413-4864-2023-3-84-93
- 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. J Oral Maxillofac Pathol. 2011;15(1):26–33. doi: 10.4103/0973-029X.80034
- Il’ina LYu, Sapozhnikov SP, Kozlov VA, et al. Quantitative evaluation of mast cells sulfation. Acta medica Eurasica. 2020;2:43–53.
- 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):698–700. EDN: LJSVYL doi: 10.1007/s10517-006-0256-3
- 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. Biochem Pharmacol. 1987;36(21):3613–3619. doi: 10.1016/0006-2952(87)90010-4
- Bhadoria P, Nagar M, Bharihoke V, Bhadoria AS. Ethephon, an organophosphorous, a fruit and vegetable ripener: has potential hepatotoxic effects? J Family Med Prim Care. 2018;7(1):179–183. doi: 10.4103/jfmpc.jfmpc_422_16
- Hussein WF, Farahat FY, Abass MA, Shehata AS. Hepatotoxic potential of gibberellic acid (GA3) in adult male albino rats. Life Sci J. 2011;8:373–383.
- Yukina GYu, Zhuravskii SG, Panevin AA, et al. Macrophage granulomas and mast cells as beginning organ remodeling in case of silicone dioxide nanoparticles chronic toxicity. Translational Medicine. 2016;3(2):70–79. EDN: XBHQTN doi: 10.18705/2311-4495-2016-3-2-70-79
- Xu L, Yang Y, Wen Y, et al. Hepatic recruitment of eosinophils and their protective function during acute liver injury. J Hepatol. 2022;77(2):344–352. doi: 10.1016/j.jhep.2022.02.024
- 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. EDN: PJYAUA doi: 10.15690/vramn1284
- Yurina NA, Radostina AI. Mast cells and their role in the body: textbook. Moscow: Peoples’ Friendship University named after Patrice Lumumba; 1977. 75 p. (In Russ.)
- Gusel’nikova VV, Pronina AP, Nazarov PG, Polevshchikov AV. Origin of mast cells: current state of the problem. In: Questions of morphology of the XXI century. Vol. 2. Collection of works dedicated to the 80-th anniversary of the birth of Aleksey Andreevich Klishov. Saint Petersburg: DEAN; 2010. P. 108–115. (In Russ.)
- 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.)
- Mayanskii AN, Pazyuk EA, Makarova TP, et al. Mechanism and diagnostic capabilities of the reaction of reduction of nitroblue tetrazolium by human neutrophils. Kazan Medical Journal. 1981;62(4):64–68. (In Russ.) EDN: NGWVRW