Extracts of pomegranate, persimmon, nettle, dill, kale and Sideritis specifically modulate gut microbiota and local cytokines production: in vivo study

Authors

DOI:

https://doi.org/10.15587/2519-8025.2020.204781

Keywords:

edible plants extracts, immunomodulation action, gut microbiota

Abstract

The aim of the work was to use the in vivo model to reveal main changes in gut microbiota of immune competent mice in dynamic and find out the specificity of immunomodulation action (activity) of traditional foods ingredients - edible plants extracts on local mucosal cytokines to its oral administration.

Materials and methods. In this study, seven groups of immunocompetent BALB/c mice were formed. All experimental mice had been fed orally by plants’ extracts (15mg/200 µl/mouse) for the 14th days. The extracts of edible plants - ingredients of traditional food such as kale leaves, persimmon, pomegranate, dill, Sideritis scardica, and nettle were obtained as described and orally administrated to experimental animals. For microbiological analysis of gut microbiota changes, the colon content has been investigated, the key microbial representatives were isolated by plating of its serial dilution on selected chromogenic medium, identified serologically and biochemically. The production of cytokines in different gut compartments and gut associated lymphoid tissues (GALT) were detected by Enzyme-linked immunosorbent assay (ELISA).

Results. In experiments in mice, the ability of Kale, Dill and Sideritis extracts, when administered orally, selectively inhibit the content of E. coli, K. pneumoniae, E. faecalis, L. acidophilus in the colon of mice had been demonstrated, and increasing of B. bifidum had been observed. Nettle extract leads to an increase in E. coli, and persimmon extract - to an increase in levels of E. faecalis, Bifidobacterium and a decrease in the content of Candida spp. Pomegranate extract specifically stimulates the growth of Bifidobacterium. There are sufficient differences in produced cytokines in fragment culture and serum of mice fed with different plants extracts. TNF-a, and IL-2 increased both systemically and locally in the different gut compartments by Dill extract, Nettle and Sideritis extracts only at mucosal sites. IL-2, but also IL-10 and IL-12, IFN-g, and IL-17 but not TNF-a were stimulated in different levels by Pomegranate, Persimmon and Kale extracts: both systemically and locally.

Conclusions. No harmful influence of tested plants had been observed. The most beneficial properties are inherent to Persimmon extract and slightly less detected in Pomegranate and Kale extracts. Siderites extract rather show no significant influence on all the studied indices while the Nettle and Dill extracts are acting pro-inflammatory

Author Biographies

Tamara Meleshko, State Higher Educational Institution «Uzhhorod National University» Narodna sq., 3, Uzhhorod, Ukraine, 88000

Senior Lecturer, Junior Researcher

Department of Clinical and Laboratory Diagnostics and Pharmacology

RDE Centre of Molecular Microbiology and Mucosal Immunology

Oleksandra Pallah, State Higher Educational Institution «Uzhhorod National University» Narodna sq., 3, Uzhhorod, Ukraine, 88000

Assistant, Junior Researcher

Department of Clinical and Laboratory Diagnostics and Pharmacology

RDE Centre of Molecular Microbiology and Mucosal Immunology

Viktor Petrov, State Higher Educational Institution «Uzhhorod National University» Narodna sq., 3, Uzhhorod, Ukraine, 88000

PhD, Assistant

Department of Clinical Disciplines

Nadiya Boyko, State Higher Educational Institution «Uzhhorod National University» Narodna sq., 3, Uzhhorod, Ukraine, 88000

Doctor of Biological Sciences, Professor, Head of Department, Director of Center

Department of Clinical and Laboratory Diagnostics and Pharmacology

RDE Centre of Molecular Microbiology and Mucosal Immunology

References

  1. Woodcock, M. E., Hollands, W. J., Konic-Ristic, A., Glibetic, M., Boyko, N., Koçaoglu, B., Kroon, P. A. (2013). Bioactive-rich extracts of persimmon, but not nettle,Sideritis, dill or kale, increase eNOS activation and NO bioavailability and decrease endothelin-1 secretion by human vascular endothelial cells. Journal of the Science of Food and Agriculture, 93 (14), 3574–3580. doi: http://doi.org/10.1002/jsfa.6251
  2. Konić-Ristić, A., Srdić-Rajić, T., Kardum, N., Aleksić-Veličković, V., Kroon, P. A., Hollands, W. J. et. al. (2013). Effects of bioactive-rich extracts of pomegranate, persimmon, nettle, dill, kale andSideritisand isolated bioactives on arachidonic acid induced markers of platelet activation and aggregation. Journal of the Science of Food and Agriculture, 93 (14), 3581–3587. doi: http://doi.org/10.1002/jsfa.6328
  3. Pallah, O. V., Meleshko, T. V., Bati, V. V., Boyko, N. V. (2019). Extracts of edible plants as beneficial microorganisms growth stimulators. Biotechnologia Acta, 12 (3), 67–74. doi: http://doi.org/10.15407/biotech12.03.067
  4. Carbonell-Capella, J. M., Barba, F. J., Esteve, M. J., Frígola, A. (2013). Quality parameters, bioactive compounds and their correlation with antioxidant capacity of commercial fruit-based baby foods. Food Science and Technology International, 20 (7), 479–487. doi: http://doi.org/10.1177/1082013213492523
  5. Moyer, R., Hummer, K., Wrolstad, R. E., Finn, C. (2002). Antioxidant compounds in diverse ribes and rubus germplasm. Acta Horticulturae, 585, 501–505. doi: http://doi.org/10.17660/actahortic.2002.585.80
  6. Correia, R. T., Borges, K. C., Medeiros, M. F., Genovese, M. I. (2012). Bioactive compounds and phenolic-linked functionality of powdered tropical fruit residues. Food Science and Technology International, 18 (6), 539–547. doi: http://doi.org/10.1177/1082013211433077
  7. Perez-Gregorio, R., Simal-Gandara, J. (2017). A Critical Review of Bioactive Food Components, and of their Functional Mechanisms, Biological Effects and Health Outcomes. Current Pharmaceutical Design, 23 (19), 2731–2741. doi: http://doi.org/10.2174/1381612823666170317122913
  8. Lankelma, J. M., Nieuwdorp, M., de Vos, W. M., Wiersinga, W. J. (2015). The gut microbiota in internal medicine: implications for health and disease. The Netherlands journal of medicine, 73 (2), 61–68.
  9. Oriach, C. S., Robertson, R. C., Stanton, C., Cryan, J. F., Dinan, T. G. (2016). Food for thought: The role of nutrition in the microbiota-gut–brain axis. Clinical Nutrition Experimental, 6, 25–38. doi: http://doi.org/10.1016/j.yclnex.2016.01.003
  10. Chung, H., Pamp, S. J., Hill, J. A., Surana, N. K., Edelman, S. M., Troy, E. B. et. al. (2012). Gut Immune Maturation Depends on Colonization with a Host-Specific Microbiota. Cell, 149 (7), 1578–1593. doi: http://doi.org/10.1016/j.cell.2012.04.037
  11. Duan, J., Chung, H., Troy, E., Kasper, D. L. (2010). Microbial Colonization Drives Expansion of IL-1 Receptor 1-Expressing and IL-17-Producing γ/δ T Cells. Cell Host & Microbe, 7 (2), 140–150. doi: http://doi.org/10.1016/j.chom.2010.01.005
  12. Atarashi, K., Tanoue, T., Shima, T., Imaoka, A., Kuwahara, T., Momose, Y. et. al. (2010). Induction of Colonic Regulatory T Cells by Indigenous Clostridium Species. Science, 331 (6015), 337–341. doi: http://doi.org/10.1126/science.1198469
  13. Manohar, M., Baumann, D. O., Bos, N. A., Cebra, J. J. (2001). Gut Colonization of Mice withactA-Negative Mutant of Listeria monocytogenesCan Stimulate a Humoral Mucosal Immune Response. Infection and Immunity, 69 (6), 3542–3549. doi: http://doi.org/10.1128/iai.69.6.3542-3549.2001
  14. Zhu, W., Lin, K., Li, K., Deng, X., Li, C. (2018). Reshaped fecal gut microbiota composition by the intake of high molecular weight persimmon tannin in normal and high-cholesterol diet-fed rats. Food & Function, 9 (1), 541–551. doi: http://doi.org/10.1039/c7fo00995j
  15. George, N. S., Cheung, L., Luthria, D. L., Santin, M., Dawson, H. D., Bhagwat, A. A., Smith, A. D. (2019). Pomegranate peel extract alters the microbiome in mice and dysbiosis caused by Citrobacter rodentium infection. Food science & nutrition, 7 (8), 2565–2576. doi: http://doi.org/10.1002/fsn3.1106

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Published

2020-04-30

How to Cite

Meleshko, T., Pallah, O., Petrov, V., & Boyko, N. (2020). Extracts of pomegranate, persimmon, nettle, dill, kale and Sideritis specifically modulate gut microbiota and local cytokines production: in vivo study. ScienceRise: Biological Science, (2 (23), 4–14. https://doi.org/10.15587/2519-8025.2020.204781

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Section

Biological Sciences