Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
1.
Dent J (Basel) ; 9(7)2021 Jul 07.
Article in English | MEDLINE | ID: mdl-34356196

ABSTRACT

Dental professionals are at increased risk of being infected with airborne pathogens such as SARS-CoV-2 because they are often exposed to droplets/aerosols production during dental treatment. To scientifically clear the effects of extraoral and oral suctions on the droplets and aerosols produced by dental treatments using an ultrasonic scaler was analyzed. The adenosine triphosphate and bacteria in droplets and aerosols produced during simulated scaling were quantitatively observed by reactions with luciferin/luciferase and incubation in culture plates to grow bacteria, respectively. The protection against spreading droplets and aerosols by oral and extraoral suctions was recognized, and the areas were limited to the left and posterior sides of the dental chair head when a right-handed dentist and dental hygienist performed scaling. Extraoral suction is a very useful tool for reducing the infection risk of COVID-19 in dental care, but the effective area is limited depending on physical characteristics of dentist and dental hygienist.

2.
PLoS One ; 12(1): e0169443, 2017.
Article in English | MEDLINE | ID: mdl-28099448

ABSTRACT

Diabetes can lead to dysfunction of the secretory capacity in salivary glands. Activation of the receptor for advanced glycation end products (RAGE) and its ligands has been suggested to participate in chronic disorders such as diabetes and its complications. In this study, the expression of RAGE, high mobility group box 1 (HMGB1) and advanced glycation end products (AGE), as well as the effects of low-power laser irradiation (LPLI) in salivary glands of diabetic rats were evaluated, and the mechanisms involved were characterized. The expression of RAGE and HMGB1 at the protein and mRNA levels was observed in submandibular glands (SMGs) of streptozotocin-induced diabetic rats. A diode laser was applied at 660 nm, 70 mW, 20 J/cm2, 0.56 J/point, with a spot area of 0.028 cm2 and its in vivo effects and the pathways involved were evaluated. Immunohistochemistry and western blotting analysis were performed for inflammatory and apoptosis markers. Diabetes up-regulates HMGB1/AGE/RAGE axis gene expression in SMGs that is associated with activation of the nuclear factor kappa B (NF-κB) pathway. Interestingly, LPLI suppresses NF-κB activation induced by inflammation. LPLI also reduces diabetes-induced apoptosis. That effect was accompanied by decreased levels of Bax, and cleaved caspase 3, which were up-regulated in diabetes. Taken together, our data suggest that LPLI reduces diabetes-induced inflammation by reducing the induction of HMGB1, ultimately leading to inhibition of apoptosis in submandibular glands of diabetic rats.


Subject(s)
Diabetes Mellitus, Experimental/complications , Sialadenitis/radiotherapy , Submandibular Gland/radiation effects , Animals , Apoptosis/radiation effects , Diabetes Mellitus, Experimental/pathology , Female , Glycation End Products, Advanced/metabolism , HMGB1 Protein/metabolism , Low-Level Light Therapy , Rats , Rats, Wistar , Receptor for Advanced Glycation End Products/metabolism , Sialadenitis/metabolism , Sialadenitis/pathology , Submandibular Gland/pathology
3.
Dent Mater ; 27(9): 926-33, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21676453

ABSTRACT

OBJECTIVES: While screening the activity of potential inhibitors of matrix metalloproteinases (MMPs), due to the limited water solubility of some of the compounds, they had to be solubilized in ethanol. When ethanol solvent controls were run, they were found to partially inhibit MMPs. Thus, the purpose of this study was to compare the MMP-inhibitory activity of a series of alcohols. METHODS: The possible inhibitory activity of a series of alcohols was measured against soluble rhMMP-9 and insoluble matrix-bound endogenous MMPs of dentin in completely demineralized dentin. Increasing concentrations (0.17, 0.86, 1.71 and 4.28 mol/L) of a homologous series of alcohols (i.e. methanol, ethanol, propanols, butanols, pentanols, hexanols, the ethanol ester of methacrylic acid, heptanols and octanol) were compared to ethanediol, and propanediol by regression analysis to calculate the molar concentration required to inhibit MMPs by 50% (i.e. the IC(50)). RESULTS: Using two different MMP models, alcohols were shown to inhibit rhMMP-9 and the endogenous proteases of dentin matrix in a dose-dependent manner. The degree of MMP inhibition by alcohols increased with chain length up to 4 methylene groups. Based on the molar concentration required to inhibit rhMMP-9 fifty percent, 2-hydroxyethylmethacrylate (HEMA), 3-hexanol, 3-heptanol and 1-octanol gave the strongest inhibition. SIGNIFICANCE: The results indicate that alcohols with 4 methylene groups inhibit MMPs more effectively than methanol or ethanol. MMP inhibition was inversely related to the Hoy's solubility parameter for hydrogen bonding forces of the alcohols (i.e. to their hydrophilicity).


Subject(s)
Alcohols/pharmacology , Dentin/enzymology , Matrix Metalloproteinase Inhibitors , Protease Inhibitors/pharmacology , Adolescent , Alcohols/chemistry , Dipeptides/pharmacology , Dose-Response Relationship, Drug , Humans , Hydrophobic and Hydrophilic Interactions , Inhibitory Concentration 50 , Recombinant Proteins , Regression Analysis , Solubility , Tooth Demineralization , Young Adult
4.
Dent Mater ; 26(8): 771-8, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20472280

ABSTRACT

OBJECTIVES: The purposes of this work were to quantitate the affinity and binding capacity of chlorhexidine (CHX) digluconate to mineralized versus demineralized dentin powder and to determine how much debinding would result from rinsing with water, ethanol, hydroxyethylmethacrylate (HEMA) or 0.5M NaCl in water. METHODS: Dentin powder was made from coronal dentin of extracted human third molars. Standard amounts of dentin powder were tumbled with increasing concentrations of CHX (0-30 mM) for 30 min at 37 degrees C. After centrifuging the tubes, the supernatant was removed and the decrease in CHX concentration quantitated by UV-spectroscopy. CHX-treated dentin powder was resuspended in one of the four debinding solutions for 3 min. The amount of debound CHX in the solvents was also quantitated by UV-spectroscopy. RESULTS: As the CHX concentration in the medium increased, the CHX binding to mineralized dentin powder also increased up to 6.8 micromol/g of dry dentin powder. Demineralized dentin powder took up significantly (p<0.01) more CHX, reaching 30.1 micromol CHX/g of dry dentin powder. Debinding of CHX was in the order: HEMA

Subject(s)
Anti-Infective Agents, Local/pharmacokinetics , Chlorhexidine/analogs & derivatives , Dental Bonding , Dentin/metabolism , Tooth Demineralization/metabolism , Anti-Infective Agents, Local/pharmacology , Chlorhexidine/pharmacokinetics , Chlorhexidine/pharmacology , Collagen/metabolism , Durapatite , Ethanol , Humans , Hydrogen Bonding , Linear Models , Matrix Metalloproteinase Inhibitors , Methacrylates , Protease Inhibitors/pharmacology , Protein Binding , Resin Cements/chemistry , Sodium Chloride , Solubility , Spectroscopy, Fourier Transform Infrared , Water
SELECTION OF CITATIONS
SEARCH DETAIL
...