References
1. Birulina J.G., Ivanov V.V., Buyko E.E., Bykov V.V., Smagliy l.V., Nosarev A.V., et al. High-fat, high-carbohydrate diet-induced experimental model of metabolic syndrome in rats. Byulleten’ sibirskoy meditsiny [Bulletin of Siberian Medicine]. 2020; 19 (4): 14–20. DOI: https://doi.org/10.20538/1682-0363-2020-4-14-20 (in Russian)
2. Shepeleva O.A. Degteva G.N., Novikova Yu.A. Food security of the Arctic and near-Arctic territories of the European North of Russia. Ekologiya cheloveka [Human Ecology]. 2019; (10): 24–32. DOI: https://doi.org/10.33396/1728-0869-2019-10-24-32 (in Russian)
3. Nikiforova N.A., Karapetyan T.A., Dorshakova N.V. Peculiarities of nutrition of the inhabitants of the North. Ekologiya cheloveka [Human Ecology]. 2018; (11): 20–2. DOI: https://doi.org/10.33396/1728-0869-2018-11-20-25 (in Russian)
4. Abd-Elhakim Y.M., Hashem M.M.M., Abo-El-Sooud K., Ali H.A., Anwar A., El-Metwally A.E., et al. Involvement of tumor necrosis factor-α, interferon gamma-γ, and interleukins 1β, 6, and 10 in immunosuppression due to long-term exposure to five common food preservatives in rats. Gene. 2020; 742: 144590. DOI: https://doi.org/10.1016/j.gene.2020.144590
5. Maier E., Kurz K., Jenny M., Schennach H., Ueberall F., Fuchs D. Food preservatives sodium benzoate and propionic acid and colorant curcumin suppress Th1-type immune response in vitro. Food Chem Toxicol. 2010; 48 (7): 1950–6. DOI: https://doi.org/10.1016/j.fct.2010.04.042
6. Weström B., Arévalo Sureda E., Pierzynowska K., Pierzynowski S.G., Pérez-Cano F.J. The immature gut barrier and its importance in establishing immunity in newborn mammals. Front Immunol. 2020; 9 (11): 1153. DOI: https://doi.org/10.3389/fimmu.2020.01153
7. Maher S., Geoghegan C., Brayden D.J. Intestinal permeation enhancers to improve oral bioavailability of macromolecules: Reasons for low efficacy in humans. Expert Opin Drug Deliv 2021; 18 (2): 273–300. DOI: https://doi.org/10.1080/17425247.2021.1825375
8. Suzuki T. Regulation of the intestinal barrier by nutrients: The role of tight junctions. Anim Sci J. 2020; 91 (1): e13357. DOI: https://doi.org/10.1111/asj.13357
9. Shukla P.K., Meena A.S., Dalal K., Canelas C., Samak G., Pierre J.F., et al. Chronic stress and corticosterone exacerbate alcohol-induced tissue injury in the gut-liver-brain axis. Sci Rep. 2021; 11 (1): 826. DOI: https://doi.org/10.1038/s41598-020-80637-y
10. Labanski A., Langhorst J., Engler H., Elsenbruch S. Stress and the brain-gut axis in functional and chronic-inflammatory gastrointestinal diseases: A transdisciplinary challenge. Psychoneuroendocrinology. 2020; 111: 104501. DOI: https://doi.org/10.1016/j.psyneuen.2019.104501
11. Spalinger M.R., Sayoc-Becerra A., Santos A.N., Shawki A., Canale V., Krishnan M., et al. PTPN2 regulates interactions between macrophages and intestinal epithelial cells to promote intestinal barrier function. Gastroenterology. 2020; 159 (5): 1763–77.e14. DOI: https://doi.org/10.1053/j.gastro.2020.07.004
12. Saito Y., Shimizu M., Iwatsuki K., Hanyu H., Tadaishi M., Sugita-Konishi Y., et al. Effect of short-time treatment with TNF-α on stem cell activity and barrier function in enteroids. Cytotechnology. 2021; 73 (4): 669–82. DOI: https://doi.org/10.1007/s10616-021-00487-y
13. Chen Z., Luo J., Li J., Kim G., Stewart A., Urban J.F. Jr, et al. Interleukin-33 promotes serotonin release from enterochromaffin cells for intestinal homeostasis. Immunity. 2021; 54 (1): 151–63.e6. DOI: https://doi.org/10.1016/j.immuni.2020.10.014
14. Kyritsi K., Kennedy L., Meadows V., Hargrove L., Demieville J., Pham L., et al. Mast cells induce ductular reaction mimicking liver injury in mice through mast cell-derived transforming growth factor beta 1 signaling. Hepatology. 2021; 73 (6): 2397–410. DOI: https://doi.org/10.1002/hep.31497
15. Paray B.A., Albeshr M.F., Jan A.T., Rather I.A. Leaky gut and autoimmunity: An intricate balance in individuals health and the diseased state. Int J Mol Sci. 2020; 21 (24): 9770. DOI: https://doi.org/10.3390/ijms21249770
16. Mohebali N., Ekat K., Kreikemeyer B., Breitrück A. Barrier protection and recovery effects of gut commensal bacteria on differentiated intestinal epithelial cells in vitro. Nutrients. 2020; 12 (8): 2251. DOI: https://doi.org/10.3390/nu12082251
17. Kim C.H. Control of lymphocyte functions by gut microbiota-derived short-chain fatty acids. Cell Mol Immunol. 2021; 18 (5): 1161–71. DOI: https://doi.org/10.1038/s41423-020-00625-0
18. Ornelas A., Dowdell A.S., Lee J.S., Colgan S.P. Microbial metabolite regulation of epithelial cell-cell interactions and barrier function. Cells. 2022; 11 (6): 944. DOI: https://doi.org/10.3390/cells11060944
19. Vojdani A. Molecular mimicry as a mechanism for food immune reactivities and autoimmunity. Altern Ther Health Med. 2015; 21 (1): 34–45.
20. Bischoff S.C., Barbara G., Buurman W., Ockhuizen T., Schulzke J.D., Serino M., et al. Intestinal permeability – a new target for disease prevention and therapy. BMC Gastroenterol. 2014; 14: 189. DOI: https://doi.org/10.1186/s12876-014-0189-7
21. Mu Q., Kirby J., Reilly C.M., Luo X.M. Leaky gut as a danger signal for autoimmune diseases. Front Immunol. 2017; 8: 598. DOI: https://doi.org/10.3389/fimmu.2017.00598
22. Shamriz O., Mizrahi H., Werbner M., Shoenfeld Y., Avni O., Koren O. Microbiota at the crossroads of autoimmunity. Autoimmun Rev. 2016; 15 (9): 859–69. DOI: https://doi.org/10.1016/j.autrev.2016.07.012
23. Rinninella E., Cintoni M., Raoul P., Gasbarrini A., Mele M.C. Food additives, gut microbiota, and irritable bowel syndrome: A hidden track. Int J Environ Res Public Health. 2020; 17 (23): 8816. DOI: https://doi.org/10.3390/ijerph17238816