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1.
J Investig Clin Dent ; 2(3): 187-96, 2011 Aug.
Article in English | MEDLINE | ID: mdl-25426790

ABSTRACT

AIM: The aim of this study was to find the oral isolate of lactobacilli, which has the potential to inhibit either periodontal, cariogenic, or fungal pathogens in vitro, and to examine the effects of bovine milk fermented with the isolate on the oral carriage of cariogenic and periodontal pathogens. METHODS: The inhibitory effects of the supernatant of Man-Rogosa-Sharpe broth, in which each of 42 oral isolates of lactobacilli grown, was examined. One isolate, Lactobacillus rhamnosus L8020, that showed the potential to inhibit either periodontal, cariogenic, or fungal pathogens in vitro, was used to examine the effects of fermented milk on the oral carriage of cariogenic and periodontal pathogens, which was examined by a placebo-controlled and cohort trial using 50 participants. RESULTS: Edible yogurt containing Lactobacillus rhamnosus L8020 significantly reduced the oral carriage of mutans streptococci (P < 0.01) and four periodontal pathogens examined: Porphyromonas gingivalis, Prevotella intermedia, Tannerella forsythia, and Fusobacterium spp. (P < 0.01), but the phenomenon were not observed with the placebo yogurt (P > 0.05). CONCLUSION: These results suggest that yogurt with Lactobacillus rhamnosus L8020 could reduce the risk of dental caries and periodontal disease.


Subject(s)
Antibiosis/physiology , Gram-Negative Bacteria/physiology , Lacticaseibacillus rhamnosus/metabolism , Mouth/microbiology , Streptococcus mutans/physiology , Yogurt/microbiology , Animals , Bacterial Load , Bacteriological Techniques , Bacteroides/physiology , Candida albicans/physiology , Cattle , Cohort Studies , Double-Blind Method , Female , Fusobacterium/physiology , Humans , Lacticaseibacillus rhamnosus/physiology , Male , Placebos , Porphyromonas gingivalis/physiology , Prevotella intermedia/physiology , Saliva/microbiology , Streptococcus sobrinus/physiology , Young Adult
2.
J Prosthodont Res ; 54(1): 1-6, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19733525

ABSTRACT

PURPOSE: To investigate the effects of titanium (Ti) ions on the cell viability, the cell differentiation and the gene expressions related to bone resorption including Receptor Activator of NF-kappaB Ligand (RANKL) and Osteoprotegerin (OPG) in the tissues around dental implants, the osteoblast-, osteoclast-, and gingival epithelial-like cells were exposed to Ti ions. METHODS: An MTS assay was carried out to evaluate the viabilities of osteoblast-like MC3T3-E1, osteoclast-like RAW264.7 and epithelial cell-like GE-1 cells. The gene expressions in these cells were analyzed by the use of RT-PCR and real-time quantitative RT-PCR. RESULTS: Ti ions in the concentration range 1-9 ppm had little effect on the viabilities of MC3T3-E1, RAW264.7 and GE-1, whereas 20 ppm Ti ions significantly decreased the viabilities of all cells. Analyses of RT-PCR and real-time quantitative RT-PCR data revealed that Ti ions at 9 ppm remarkably inhibited the expressions of Runx2, Osterix and type I collagen in MC3T3-E1. In RAW264.7, Ti ions showed no effects on the levels of mRNAs for TRAP and cathepsin K enhanced by RANKL. Ti ions at the range of 1-9 ppm showed no effects on the levels of mRNAs for RANKL and OPG in GE-1, while Ti ions at 9 ppm enhanced the expression of these genes in MC3T3-E1. CONCLUSIONS: These results, taken together, suggested that Ti ions show the biological effects, both on the viabilities of osteoblast and osteoclast and on the differentiation of either the osteoblastic or osteoclastic cells, which may influence the prognosis of dental implants.


Subject(s)
Cell Differentiation/drug effects , Cell Survival/drug effects , Dental Implants , Epithelial Cells/cytology , Gingiva/cytology , Osteoblasts/cytology , Osteoclasts/cytology , Titanium/adverse effects , Animals , Bone Remodeling/drug effects , Bone Resorption/genetics , Cell Differentiation/genetics , Cells, Cultured , Depression, Chemical , Dose-Response Relationship, Drug , Gene Expression/drug effects , Ions , Mice , Osteoprotegerin , RANK Ligand
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