EFFECT OF GLUTAMATE-INDUCED OBESITY ON THE METABOLIC PROFILE OF THE LIVER AND CORRECTION BY MULTIPROBIOTIC OR NANOCRYSTALLINE CERIUM DIOXIDE

Authors

  • M. M. Kondro DANYLO HALYTSKY LVIV NATIONAL MEDICAL UNIVERSITY
  • B. M. Verveha DANYLO HALYTSKY LVIV NATIONAL MEDICAL UNIVERSITY
  • T. V. Beregova EDUCATIONAL AND SCIENTIFIC CENTRE "INSTITUTE OF BIOLOGY AND MEDICINE" AT TARAS SHEVCHENKO NATIONAL UNIVERSITY OF KYIV
  • М. Ya. Spivak INSTITUTE OF MICROBIOLOGY AND VIROLOGY NAMED AFTER D. K. ZABOLOTNY, NATIONAL ACADEMY OF SCIENCES OF UKRAINE

DOI:

https://doi.org/10.11603/mcch.2410-681X.2024.i1.14593

Keywords:

МАРІЯ ТИХА, obesity, hepatic steatosis, multi-probiotic, nanocrystalline cerium dioxide

Abstract

Introduction. Currently, there is no unidirectional formulation regarding the mechanisms of the pathogenesis of steatohepatosis and its connection with accompanying pathologies, which generally determines the relevance of research.

The aim of the study – to characterize the corrective effect of the multiprobiotic “Symbiter acidophilic” concentrated or nanocrystalline cerium dioxide on the formation of steatohepatosis induced by neonatal sodium glutamate administration.

Research Methods. The experiments were carried out on white non-linear male rats, the direction included the study of the mechanisms of development of steatohepatosis in rats for 16 weeks, which were administered monosodium glutamate in the neonatal period and the study of the structural and functional state of the liver in rats after neonatal administration of monosodium glutamate against the background of periodic administration of a multiprobiotic or nanocrystalline dioxide cerium.

Results and Discussion. It was established that neonatal sodium glutamate administration causes metabolic changes in 16-week-old rats, which are manifested in disproportionate accumulation of fat with the development of visceral obesity, dyslipidemia, and steatohepatosis. In rats, after neonatal administration of monosodium glutamate, lipid metabolism was disturbed, which was manifested in an increase in the concentration of triglycerides, total cholesterol, low and very low density lipoproteins and a decrease in the concentration of high density lipoproteins. Periodic administration of a multiprobiotic or nanocrystalline cerium dioxide to rats after neonatal sodium glutamate administration significantly normalized lipid metabolism indicators.

Conclusions. In rats injected with monosodium glutamate in the neonatal period, periodic use of the multiprobiotic “Symbiter acidophilic” concentrated or nanocrystalline cerium dioxide significantly restored the morpho-functional state of the liver, reduced the manifestations of oxidative stress and prevented the development of steatohepatosis, which indicates the antioxidant effect of these drugs and the possibility of their use for the prevention of steatohepatosis.

References

Filipova, O.Yu. (2010). The state of lipid peroxidation and the antioxidant defense system in patients with non-alcoholic steatosis of the liver with pathology of the biliary tract. Herald of Morphology, 16(4), 831-834.

Schuppan, D., Schattenberg, J.M. (2013). Non-alcoholic steatohepatitis: pathogenesis and novel therapeutic approaches. J. Gastroenterol. Hepatol., 28 (Suppl. 1), 68-76.

Tannapfel, A., Denk, H., Dienes, H.P., Langner, C., Schirmacher, P., Trauner, M. (2011). Histopathological diagnosis of non-alcoholic and alcoholic fatty liver disease. Virchows Arch., 458 (5), 511-523.

Tacer, F.К., Rozman, D. (2011). Nonalcoholic Fatty Liver Disease: Focus on Lipoprotein and Lipid Deregulation. Journal of Lipids, 2, 1-14.

Jia, W., Rajani, C. (2018). The Influence of Gut Microbial Metabolism on the Development and Progression of Non-alcoholic Fatty Liver Disease. Adv. Exp. Med. Biol., 1061, 95-110.

Gerard, C., Vidal, H. (2019). Impact of Gut Microbiota on Host Glycemic Control. Front. Endocrinol. (Lausanne). 10, 29. DOI. 10.3389/fendo.2019.00029.

Savcheniuk, O., Kobyliak, N., Kondro, М., Vir­chenko, O., Falalyeyeva, T., Beregova, T. (2014). Short-term periodic consumption of multiprobiotic from childhood improves insulin sensitivity, prevents development of non-alcoholic fatty liver disease and adiposity in adult rats with glutamate-induced obesity. BMC Complementary and Alternative Medicine, 14, 247.

Nakanishi, Y., Tsuneyama, K., Fujimoto, M., Salunga, T.L. (2008). Monosodium glutamate (MSG): a villain and promoter of liver inflammation and dysplasia. J. Autoimmunity, 30(1-2), 42-50.

Kondro, M., Kobyliak, N., Virchenko, O., Falalyeyeva, T., Beregova, T., Bodnar, P. (2015). Multiprobiotic therapy from childhood prevents the development of nonalcoholic fatty liver disease in adult monosodium glutamate-induced obese rats. Current Issues in Pharmacy and Medical Sciences, 27 (4), 243-245.

Bernardis, L.L., Patterson, B.D. (1968). Correlation between “Li index” and carcass fat content in weanling and adult female rats with hypothalamic lessions. J. Endocrinol., 40, 527-528.

Fossmark, R., Qvigstad, G., Waldum, H. (2008). Gastric cancer: animal studies on the risk of hypoacidity and hypergastrinemia. World Journal of Gastroenterology, 14(11), 1646-1651.

Fabbrini, E., Sullivan, S., Klein, S. (2010). Obesity and nonalcoholic fatty liver disease: biochemical, metabolic, and clinical implications. Hepatology, 51(2), 679-689. DOI: 10.1002/hep.23280.

Tuohya, K.M., Favaa, F., Viola, R. (2014). The way to a man’s heart is through his gut microbiota – dietary pro- and prebiotics for management of cardiovascular risk. Proceedings of the Nutrition Society, 73, 172-185.

Ejtahed, H.S., Mohtadi-Nia, J., Homayouni-Rad, A., Niafar, M., Asghari-Jafarabadi, M., Mofid, V., Akbarian-Moghari, A. (2011). Effect of probiotic yogurt containing Lactobacillus acidophilus and Bifidobacterium lactis on lipid profile in individuals with type 2 diabetes mellitus. J. Dairy Sci., 94 (7), 3288-3294.

Kawase, M., Hashimoto, H., Hosoda, M. (2000). Effect of administration of fermented milk containing whey protein concentrate to rats and healthy men on serum lipids and blood pressure. J. Dairy Sci., 83(2), 255-263.

Xiao, J.Z., Kondo, S., Takahashi, N. (2003). Effects of milk products fermented by Bifidobacterium longum on blood lipids in rats and healthy adult male volunteers. Dairy Sci., 86 (7), 2452-2461.

Martin, F.P., Wang, Y., Sprenger, N. (2008). Probiotic modulation of symbiotic gut microbial-host metabolic interactions in a humanized microbiome mouse model. Mol. Syst. Biol., 4, 157. DOI: 10.1038/msb4100190.

Wang, Y., Xu, N., Xi, A. (2009). Effect of Lactobacillus plantarum MA2 isolated from Tibet kefir on lipid metabolism and intestinal microflora of rats fed on high-cholesterol diet. Appl. Microbiol. Biotechnol., 84(2), 341-347.

Fedorak, R.N., Madsen, K.L. (2004). Probiotics and Prebiotics in Gastrointestinal Disorders. Curr. Opin. Gastroenterol., 20(2), 146-155.

Park, Y.H., Kim, J.G., Shin, Y.W., Kim, S.H., Whang, K.Y. (2007). Effect of dietary inclusion of Lactobacillus acidophilus ATCC 43121 on cholesterol metabolism in rats. J. Microbiol. Biotechnol., 17, 655-662.

Jeun, J., Kim, S., Cho, S.Y., Jun, H.J., Park, H.J., Seo, J.G., Chung, M.J., Lee, S.J. (2009). Hypocholesterolemic effects of Lactobacillus plantarum KCTC3928 by increased bile acid excretion in C57BL/6 mice. Nutrition, 26, 321-330.

Mathara, J.M., Schillinger, U., Guigas, C., Franz, C., Kutima, P.M,, Mbugua, S.K., Shin, H.K., Holzapfel, W.H. (2008) Functional characteristics of Lactobacillus spp. From traditional Maasai fermented milk products in Kenya. Int. J. Food Microbiol., 126, 57-64.

Published

2024-04-29

How to Cite

Kondro, M. M., Verveha, B. M., Beregova, T. V., & Spivak М. Y. (2024). EFFECT OF GLUTAMATE-INDUCED OBESITY ON THE METABOLIC PROFILE OF THE LIVER AND CORRECTION BY MULTIPROBIOTIC OR NANOCRYSTALLINE CERIUM DIOXIDE. Medical and Clinical Chemistry, (1), 18–26. https://doi.org/10.11603/mcch.2410-681X.2024.i1.14593

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Section

ORIGINAL INVESTIGATIONS