Effects of culture supernatants of MG5346 (CS-MG5346) on receptor activator of nuclear factor-kappa B ligand (RANKL)-induced osteoclastogenesis were examined. CS-MG5346 treatment up to 400 μg/mL significantly reduced tartrate-resistant acid-phosphatase (TRAP) activity, the phenotype biomarker of osteoclast, without affecting cell viability. CS-MG5346 inhibited the expression of osteoclast specific transcriptional factors (c-fos and nuclear factor-activated T cells c1) and their target genes (, , ) in a dose-dependent manner (p<0.05). The administration of MG5346 (2×10 CFU/day) for 8 wks significantly improved furcation involvement, but no difference was observed in alveolar bone loss in ligature-induced experimental periodontitis rats. The elevated RANKL/ osteoprotegerin ratio, the biomarker of periodontitis, was significantly lowered in the gingival tissue by administration of MG5346 (p<0.05). MG5346 showed excellent stability in simulated stomach and intestinal fluids and did not have antibiotic resistance. Based on the results, MG5346 has the potential to be a promising probiotic strain for oral health.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890358PMC
http://dx.doi.org/10.5851/kosfa.2022.e68DOI Listing

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