The transcription factor, hypoxia‐inducible factor‐1α (HIF‐1α), has previously been shown to upregulate the expression of hypoxia‐related genes, including erythropoietin (EPO). However, the role of hypoxia‐inducible factor‐1α in morphogenesis during salivary gland development is unclear. We investigated the function of HIF‐1α in submandibular gland (SMG) organ cultures obtained from embryonic day 13.5 embryos from ICR female mice. Expression of HIF‐1α, glucose transporter 1, and vascular endothelial growth factor was induced under hypoxia (5% O2). We further showed that BAY 87‐2243‐mediated inhibition of HIF‐1α suppressed salivary gland development. Under severe hypoxia (1% O2), HIF‐1α did not promote salivary gland development; this was due to suppression of cell proliferation and inhibition of the cell cycle and not because of autophagy and apoptosis. Additionally, using the inhibitor U0126, we verified that the ERK1/2 pathway is upstream of HIF‐1α. Overall, we found that the HIF‐1α signaling pathway plays a critical role in salivary gland development in ex vivo SMG organ cultures.
Aim
Matching transformation system (MA‐T) is an on‐demand aqueous chlorine dioxide solution that realizes excellent safety with various antimicrobial activities even under abundant organic compound. By using MA‐T in human oral care, we examined its effectiveness against bacteria causing oral infections such as periodontal disease and dental caries.
Materials and Methods
The participants of the 75th Annual Meeting of the Japanese Stomatological Society held on May 13 and 14, 2021, were enrolled in this study. Saliva samples were collected on the first day after normal oral care and on the second day after oral care with MA‐T. The total number of bacteria and the numbers of Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola, Streptococcus mutans, and Candida albicans were compared for the two samples on Days 1 and 2.
Results
Twenty‐two subjects met the study criteria. The total bacterial count and the number of T. forsythia on Day 2 were significantly lower than those on Day 1 (p = 0.000177 and p = 0.0186, respectively). The numbers of T. denticola and S. mutans tended to decrease, although not significantly (p = 0.100 and p = 0.251, respectively). Statistical analysis was not performed for P. gingivalis and C. albicans because of sample size.
Conclusion
MA‐T is putatively effective for oral hygiene. MA‐T oral care reduces bacteria that cause periodontal disease and dental caries compared with regular oral care. The results of this study suggest that MA‐T, a new disinfectant, can be applied to oral care and may reduce periodontal disease, dental caries, and other oral infections.
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