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Intestinal microbiota regulates colonic inflammation in fluorosis mice by TLR/NF-κB pathway through short-chain fatty acids

Zhang, Shaosan, Zhao, Taotao, Wang, Yu, Mi, Jiahui, Liu, Jie, Fan, Xinyu, Niu, Ruiyan, Sun, Zilong·2023·Food and Chemical Toxicology

Abstract

Intestinal inflammation and microbial dysbiosis are found simultaneously in patients with fluorosis. However, whether the inflammation derived from fluoride exposure only or intestinal microbial disorders has not been clarified. In this study, 100 mg/L NaF exposure for 90 days significantly elevated the expressions of inflammatory factors (TNF-α, IL-1β, IL-6, IFN-γ, TGF-β, and IL-10), and the levels of TLR4, TRAF6, Myd88, IKKβ, and NF-κB P65 in mouse colon, while the above factors were reduced in pseudo germ-free mice with fluorosis, hinting that disordered microbiota might play a more direct role in the development of colonic inflammation than fluoride. Fecal microbiota transplantation (FMT) lowered the levels of inflammatory factors and inactivated the TLR/NF-κB pathway in fluoride-exposed mice. In addition, supplementing short-chain fatty acids (SCFAs) exhibited the identical effects to the model of FMT. In summary, intestinal microbiota may alleviate the colonic inflammatory of mice with fluorosis by regulating TLR/NF-κB pathway through SCFAs.

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Research works printed but not linked: 45

  1. Agalakova, 2012, Molecular mechanisms of cytotoxicity and apoptosis induced by inorganic fluoride, Int. Sch. Res. Notices
  2. Alexander, 2017, Gut microbiota modulation of chemotherapy efficacy and toxicity, Nat. Rev. Gastroenterol. Hepatol., 14, 356, 10.1038/nrgastro.2017.20 · DOI · Paper page
  3. Anthoney, 2018, Toll and Toll-like receptor signalling in development, Development, 145, dev156018, 10.1242/dev.156018 · DOI
  4. Battaglioli, 2018, Clostridioides difficile uses amino acids associated with gut microbial dysbiosis in a subset of patients with diarrhea, Sci. Transl. Med., 10, 10.1126/scitranslmed.aam7019 · DOI
  5. Cao, 2020, Intestinal fungal dysbiosis in mice induced by fluoride, Chemosphere, 245, 10.1016/j.chemosphere.2019.125617 · DOI
  6. Chen, 2021, Role and mechanism of gut microbiota in human disease, Front. Cell. Infect. Microbiol., 11
  7. Erny, 2015, Host microbiota constantly control maturation and function of microglia in the CNS, Nat. Neurosci., 18, 965, 10.1038/nn.4030 · DOI · Paper page
  8. Follin-Arbelet, 2016, Fluoride: a risk factor for inflammatory bowel disease?, Scand. J. Gastroenterol., 51, 1019, 10.1080/00365521.2016.1177855 · DOI
  9. Fordyce, 2007, A health risk assessment for fluoride in Central Europe, Environ. Geochem. Health, 29, 83, 10.1007/s10653-006-9076-7 · DOI
  10. Fu, 2020, Fluoride-induced alteration in the diversity and composition of bacterial microbiota in mice colon, Biol. Trace Elem. Res., 196, 537, 10.1007/s12011-019-01942-w · DOI · Paper page
  11. Fu, 2022, Exercise alleviated intestinal damage and microbial disturbances in mice exposed to fluoride, Chemosphere, 288
  12. Garantziotis, 2022, Proteoglycans in Toll-like receptor responses and innate immunity, Am. J. Physiol. Cell Physiol., 323, C202, 10.1152/ajpcell.00088.2022 · DOI
  13. He, 2019, The functional role of fecal microbiota transplantation on dextran sulfate sodium-induced colitis in mice, Front. Cell. Infect. Microbiol., 9, 393, 10.3389/fcimb.2019.00393 · DOI
  14. Jagtap, 2012, Fluoride in drinking water and defluoridation of water, Chem. Rev., 112, 2454, 10.1021/cr2002855 · DOI
  15. Kawai, 2007, Signaling to NF-kappaB by toll-like receptors, Trends Mol. Med., 13, 460, 10.1016/j.molmed.2007.09.002 · DOI
  16. Kim, 2013, Short-chain fatty acids activate GPR41 and GPR43 on intestinal epithelial cells to promote inflammatory responses in mice, Gastroenterology, 145, 396, 10.1053/j.gastro.2013.04.056 · DOI · Paper page
  17. Lepage, 2011, Twin study indicates loss of interaction between microbiota and mucosa of patients with ulcerative colitis, Gastroenterology, 141, 227, 10.1053/j.gastro.2011.04.011 · DOI
  18. Li, 2020, Self-recovery study of the adverse effects of fluoride on small intestine: involvement of pyroptosis induced inflammation, Sci. Total Environ., 742, 10.1016/j.scitotenv.2020.140533 · DOI
  19. Macpherson, 2000, A primitive T cell-independent mechanism of intestinal mucosal IgA responses to commensal bacteria, Science, 288, 2222, 10.1126/science.288.5474.2222 · DOI
  20. Martin-Gallausiaux, 2021, SCFA: mechanisms and functional importance in the gut, Proc. Nutr. Soc., 80, 37, 10.1017/S0029665120006916 · DOI
  21. Miao, 2020, Alterations in cecal microbiota and intestinal barrier function of laying hens fed on fluoride supplemented diets, Ecotoxicol. Environ. Saf., 193, 10.1016/j.ecoenv.2020.110372 · DOI · Paper page
  22. Nasef, 2014, Anti-inflammatory activity of fruit fractions in vitro, mediated through toll-like receptor 4 and 2 in the context of inflammatory bowel disease, Nutrients, 6, 5265, 10.3390/nu6115265 · DOI
  23. Perumal, 2013, A brief review on experimental fluorosis, Toxicol. Lett., 223, 236, 10.1016/j.toxlet.2013.09.005 · DOI
  24. Pils, 2011, Commensal gut flora reduces susceptibility to experimentally induced colitis via T-cell-derived interleukin-10, Inflamm. Bowel Dis., 17, 2038, 10.1002/ibd.21587 · DOI
  25. Prystupa, 2011, Fluorine--a current literature review. An NRC and ATSDR based review of safety standards for exposure to fluorine and fluorides, Toxicol. Mech. Methods, 21, 103, 10.3109/15376516.2010.542931 · DOI
  26. Rath, 1996, Normal luminal bacteria, especially Bacteroides species, mediate chronic colitis, gastritis, and arthritis in HLA-B27/human beta2 microglobulin transgenic rats, J. Clin. Invest., 98, 945, 10.1172/JCI118878 · DOI
  27. Rocha, 2013, In vitro study of intestinal transport of fluoride using the Caco-2 cell line, Food Chem. Toxicol., 55, 156, 10.1016/j.fct.2012.12.037 · DOI
  28. Smith, 2013, The microbial metabolites, short-chain fatty acids, regulate colonic Treg cell homeostasis, Science, 341, 569, 10.1126/science.1241165 · DOI · Paper page
  29. Strober, 2007, The fundamental basis of inflammatory bowel disease, J. Clin. Invest., 117, 514, 10.1172/JCI30587 · DOI
  30. Susheela, 2014, Early diagnosis and complete recovery from fluorosis through practice of interventions, J. Assoc. Phys. India, 62, 572
  31. Tan, 2019, Fecal microbiota transplantation (FMT) for C. difficile infection, just say 'No', Anaerobe, 60, 10.1016/j.anaerobe.2019.102092 · DOI
  32. Tian, 2023, Identifying serum metabolites and gut bacterial species associated with nephrotoxicity caused by arsenic and fluoride exposure, Biol. Trace Elem. Res., 10.1007/s12011-023-03568-5 · DOI · Paper page
  33. Veltkamp, 2001, Continuous stimulation by normal luminal bacteria is essential for the development and perpetuation of colitis in Tg(epsilon26) mice, Gastroenterology, 120, 900, 10.1053/gast.2001.22547 · DOI
  34. Villéger, 2019, Intestinal microbiota: a novel target to improve anti-tumor treatment?, Int. J. Mol. Sci., 20, 4584, 10.3390/ijms20184584 · DOI
  35. Wang, 2021, Effect of exercise on microglial activation and transcriptome of hippocampus in fluorosis mice, Sci. Total Environ., 760, 10.1016/j.scitotenv.2020.143376 · DOI
  36. Whitford, 1994, Intake and metabolism of fluoride, Adv. Dent. Res., 8, 5, 10.1177/08959374940080011001 · DOI
  37. Wu, 2019, Fluoride induces autoimmune orchitis involved with enhanced IL-17a secretion in mice testis, J. Agric. Food Chem., 67, 13333, 10.1021/acs.jafc.9b05789 · DOI
  38. Xiao, 2020, An ecological framework to understand the efficacy of fecal microbiota transplantation, Nat. Commun., 11, 3329, 10.1038/s41467-020-17180-x · DOI · Paper page
  39. Xin, 2020, Lactobacillus johnsonii BS15 improves intestinal environment against fluoride-induced memory impairment in mice-a study based on the gut-brain axis hypothesis, PeerJ, 8, 10.7717/peerj.10125 · DOI
  40. Xin, 2021, Preventive effects of Lactobacillus johnsonii on the renal injury of mice induced by high fluoride exposure: insights from colonic microbiota and co-occurrence network analysis, Ecotoxicol. Environ. Saf., 228, 10.1016/j.ecoenv.2021.113006 · DOI · Paper page
  41. Xu, 2021, Cross-talk between butyric acid and gut microbiota in ulcerative colitis following fecal microbiota transplantation, Front. Microbiol., 12
  42. Yang, 2013, Intestinal microbiota composition of interleukin-10 deficient C57BL/6J mice and susceptibility to Helicobacter hepaticus-induced colitis, PLoS One, 8, 10.1371/journal.pone.0070783 · DOI
  43. Yasmin, 2014, Haematological changes in fluorotic adults and children in fluoride endemic regions of Gaya district, Bihar, India, Environ. Geochem. Health, 36, 421, 10.1007/s10653-013-9570-7 · DOI · Paper page
  44. Yu, 2022, Moderate exercise relieves fluoride-induced liver and kidney inflammatory responses through the IKKβ/NFκB pathway, Environ. Sci. Pollut. Res. Int., 29, 78429, 10.1007/s11356-022-21360-1 · DOI
  45. Zhu, 2022, Fluoride exposure cause colon microbiota dysbiosis by destroyed microenvironment and disturbed antimicrobial peptides expression in colon, Environ. Pollut., 292

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Metadata

Authors
Zhang, S., Zhao, T., Wang, Y., Mi, J., Liu, J., Fan, X., Niu, R., & Sun, Z.
Venue
Food and Chemical Toxicology
Publisher
Elsevier BV
Published
2023-08
Volume
178
Pages
113866
ISSN
0278-6915
Cited by
25
References
0
Language
en
Funders
Shanxi Agricultural University

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