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1.
Article in English | MEDLINE | ID: mdl-33114677

ABSTRACT

Many countries provide preventive dental care for children to reduce inequalities. In Korea, the registered dentists' program was implemented to promote oral health and prevent oral diseases in primary school students. This study aimed to evaluate the registered dentist program through the sealant utilization rate using national cohort data and to compare the socioeconomic gap of the cohorts by participation. The sample cohort data were obtained from the National Health Insurance Sharing Service (NHISS) in South Korea. The utilization of dental sealants was analyzed using the chi-square test according to the independent variables of each year. To identify the independent effects of participation in the registered dentists' program, a panel logistic regression analysis of the utilization of dental sealants was performed. The participants were 1.35 times more likely to have dental sealants than non-participants. The significance of income quintiles disappeared in the case groups. The gap became more obvious in the employees of the control group even after adjusting for all variables. Implementing oral health programs can alleviate inequality with a relative increase in utilization in vulnerable populations.


Subject(s)
Dental Caries , Dentistry/organization & administration , Pit and Fissure Sealants , Socioeconomic Factors , Chi-Square Distribution , Child , Dental Caries/epidemiology , Dental Caries/prevention & control , Humans , Program Evaluation , Republic of Korea
2.
J Microbiol Biotechnol ; 30(4): 604-614, 2020 Apr 28.
Article in English | MEDLINE | ID: mdl-31893610

ABSTRACT

The application of steroids has steadily increased thanks to their therapeutic effects. However, alternatives are required due their severe side effects; thus, studies on the activities of steroid derivatives are underway. Sugar derivatives of nandrolone, which is used to treat breast cancer, as well as cortisone and prednisone, which reduce inflammation, pain, and edema, are unknown. We linked O-glucose to nandrolone and testosterone using UDP-glucosyltransferase (UGT-1) and, then, tested their bioactivities in vitro. Analysis by NMR showed that the derivatives were 17ß-nandrolone ß-D-glucose and 17ß-testosterone ß-D-glucose, respectively. The viability was higher and cytotoxicity was evident in PC12 cells incubated with rotenone and, testosterone derivatives, compared to the controls. SH-SY5Y cells incubated with H2O2 and nandrolone derivatives remained viable and cytotoxicity was attenuated. Both derivatives enhanced neuronal protective effects and increased the amounts of cellular ATP.


Subject(s)
Bacillaceae/enzymology , Glucosyltransferases/metabolism , Glycosides/metabolism , Testosterone Congeners/metabolism , Adenosine Triphosphate/metabolism , Animals , Bacterial Proteins/metabolism , Biotransformation , Cell Line, Tumor , Energy Metabolism/drug effects , Glucose/chemistry , Glucose/metabolism , Glycosides/chemistry , Glycosides/pharmacology , Humans , Nandrolone/chemistry , Nandrolone/metabolism , Neuroprotective Agents/chemistry , Neuroprotective Agents/metabolism , Neuroprotective Agents/pharmacology , PC12 Cells , Rats , Testosterone/chemistry , Testosterone/metabolism , Testosterone Congeners/chemistry , Testosterone Congeners/pharmacology
3.
Steroids ; 145: 32-38, 2019 05.
Article in English | MEDLINE | ID: mdl-30753844

ABSTRACT

Recently, studies on the steroidal hormone activity in the brain have attracted attention, and the influences of the varied glucosides and their artificial derivatives have been discussed; additionally, it has been suggested that glucosides are the synthetic precursors of glucuronide as a label molecule. However, glucosides are formed with 11α-hydroxyprogesterone (1), which is important as a blood pressure regulator, but anti-androgen activity remains unknown. Using UDP-glucosyltransferase, glucoside synthesis was successful in linking ß-d-glucopyranose and ß-d-laminaribiose to 11α oxygen of 1 at a high conversion ratio, and full assignment structure was analyzed for the two glucosides by high-resolution quadrupole-time flight electrospray ionization-mass spectrometry, 1D (1H and 13C) NMR and 2D (COSY, ROESY, HSQC-DEPT and HMQC) NMR. Furthermore, the bioactivity of 1 and two 11α-hydroxyprogesterone glucosides [11α-(ß-d-glucopyranosyl)oxyprogesterone, 2, and 11α-(ß-d-laminaribiosyl)oxyprogesterone, 3] was tested in vitro. On rotenone-induced PC12 cells, the two 11α-hydroxyprogesterone glucosides (2 and 3) showed superior neuroprotective effects and increased cellular ATP levels compared with those of 1.


Subject(s)
Glucosides/chemistry , Glucosyltransferases/metabolism , Hydroxyprogesterones/chemistry , Hydroxyprogesterones/metabolism , Neuroprotective Agents/chemistry , Neuroprotective Agents/metabolism , Animals , Biotransformation , Hydroxyprogesterones/pharmacology , Neuroprotective Agents/pharmacology , PC12 Cells , Rats
4.
Molecules ; 23(7)2018 Jul 19.
Article in English | MEDLINE | ID: mdl-30029555

ABSTRACT

Glucosylation of the 21-hydroxyl group of glucocorticoid changes its solubility into hydrophilicity from hydrophobicity and, as with glucocorticoid glucuronides as a moving object in vivo, it is conceivable that it exhibits the same behavior. Therefore, glucosylation to the 21-hydroxyl group while maintaining the 11ß-hydroxyl group is particularly important, and glucosylation of corticosterone was confirmed by high-resolution mass spectrometry and 1D (¹H and 13C) and 2D (COSY, ROESY, HSQC-DEPT and HMBC) NMR. Moreover, the difference in bioactivity between corticosterone and corticosterone 21-glucoside was investigated in vitro. Corticosterone 21-glucoside showed greater neuroprotective effects against H2O2-induced cell death and reactive oxygen species (ROS) compared with corticosterone. These results for the first time demonstrate that bioconversion of corticosterone through the region-selective glucosylation of a novel compound can present structural potential for developing new neuroprotective agents.


Subject(s)
Corticosterone/chemistry , Corticosterone/metabolism , Glucosides/chemistry , Glucosides/metabolism , Glucosyltransferases/metabolism , Cell Line, Tumor , Cell Survival , Chromatography, High Pressure Liquid , Glucocorticoids/chemistry , Glucocorticoids/metabolism , Glycosylation , Humans , Magnetic Resonance Spectroscopy , Molecular Structure , Reactive Oxygen Species/metabolism
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