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1.
Eur Arch Paediatr Dent ; 22(4): 611-618, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33423208

ABSTRACT

PURPOSE: Parents find it challenging to follow recommendations to brush young children after feeds at night despite the increase caries risk. This study compared three clinical recommendations (dilution, rinsing and wiping) on plaque pH after formula consumption. METHODS: Eighteen subjects were recruited. The five interventions with 2-week washout between visits included: Rinse with undiluted formula for 30 s (UF); rinse with 50% diluted formula for 30 s (DF); rinse with undiluted formula for 30 s, followed by rinsing with water for 1 minute (UF/R); rinse with undiluted formula for 30 s, followed by wiping (UF/W); rinse with 10% sucrose for 30 s as control (C). Plaque samples were collected at baseline, 2, 5, 10, 20 and 30 min after the intervention and pH measured using the plaque sampling method. RESULTS: UF/R resulted in significantly smaller pH drops at 5, 10 and 20 min compared to UF. It also resulted in higher minimum pH (UF/R: 6.34 ± 0.36 Vs UF: 6.06 ± 0.40, p = 0.02), smaller maximum pH drop (UF/R: 0.63 ± 0.35 Vs UF: 0.90 ± 0.49, p = 0.03), smaller sum of change of hydrogen ion concentration (UF/R: 9.22 × 10-7 ± 7.8 × 10-7 Vs UF: 2.30 × 10-6 ± 2.6 × 10-6, p = 0.04), and smaller area under the curve (UF/R: 7.70 ± 5.44 Vs UF: 13.44 ± 9.44, p = 0.02). DF and UF/W did not result in any significant pH change compared to UF. CONCLUSIONS: Of the three clinical recommendations, only rinsing with water for 1 min after undiluted formula reduced plaque acidogenicity. Teeth wiping with a moist cloth and 50% dilution of infant formula did not have an effect on plaque acidity.


Subject(s)
Dental Plaque , Water , Animals , Child , Child, Preschool , Dental Plaque/prevention & control , Humans , Hydrogen-Ion Concentration , Milk , Sucrose
2.
J Asian Nat Prod Res ; 8(3): 223-7, 2006.
Article in English | MEDLINE | ID: mdl-16864428

ABSTRACT

A new sesquiterpenoid, O-methyl nakafuran-8 lactone (1) has been isolated from a Hainan sponge Dysidea sp. and the structure of the new compound proposed by spectral data, was confirmed by X-ray diffraction analysis. The complete 1H- and 13C-NMR assignments were made on the basis of detailed 2D NMR spectral analysis. Compound 1 showed strong inhibitory bioactivity against PTP1B with IC50 value of 1.58 microM.


Subject(s)
Porifera/chemistry , Sesquiterpenes/chemistry , Animals , Inhibitory Concentration 50 , Molecular Structure , Protein Tyrosine Phosphatase, Non-Receptor Type 1 , Protein Tyrosine Phosphatases/antagonists & inhibitors , Sesquiterpenes/isolation & purification , X-Ray Diffraction
3.
J Nat Prod ; 64(10): 1301-4, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11678655

ABSTRACT

Five new (1-3, 5, and 7) and two known (4, 6) furanosesterterpene tetronic acids were isolated from the marine sponge Sarcotragus sp. by bioactivity-guided fractionation. These compounds showed cytotoxicity against a panel of five human tumor cell lines. The gross structures were established on the basis of NMR and MS analyses. The compounds showed interesting variations of geometry and absolute configuration.


Subject(s)
Antineoplastic Agents/isolation & purification , Furans/isolation & purification , Porifera/chemistry , Terpenes/isolation & purification , Animals , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Artemia/drug effects , Chromatography, High Pressure Liquid , Circular Dichroism , Colonic Neoplasms , Drug Screening Assays, Antitumor , Female , Furans/chemistry , Furans/pharmacology , Humans , Inhibitory Concentration 50 , Korea , Larva/drug effects , Lung Neoplasms , Magnetic Resonance Spectroscopy , Molecular Structure , Neoplasms, Nerve Tissue , Ovarian Neoplasms , Skin Neoplasms , Spectrophotometry, Infrared , Spectroscopy, Fourier Transform Infrared , Stereoisomerism , Structure-Activity Relationship , Terpenes/chemistry , Terpenes/pharmacology , Tumor Cells, Cultured/drug effects
4.
J Nat Prod ; 64(6): 767-71, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11421740

ABSTRACT

Erylosides G--J (1--4), four new triterpenoid saponins, were isolated from the sponge Erylus nobilis collected from Jaeju Island, Korea. On the basis of the results of combined chemical and spectral analyses, the structures of the aglycones were determined to be lanostane-based, modified penasterols. The oligosaccharide portions were composed of one unit each of L-arabinose, D-galactose, and 2-N-acetyl-D-glucosamine (1 and 3) or two units of L-arabinose and one unit of 2-N-acetyl-D-glucosamine (2 and 4). These compounds exhibited moderate cytotoxicty against a human leukemia cell line.


Subject(s)
Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Porifera/chemistry , Saponins/chemistry , Triterpenes/chemistry , Animals , Antineoplastic Agents/isolation & purification , Drug Screening Assays, Antitumor , Humans , Hydrolysis , Immunosuppressive Agents/chemistry , Immunosuppressive Agents/isolation & purification , Immunosuppressive Agents/pharmacology , Korea , Magnetic Resonance Spectroscopy , Oligosaccharides/chemistry , Platelet Aggregation Inhibitors/chemistry , Platelet Aggregation Inhibitors/isolation & purification , Platelet Aggregation Inhibitors/pharmacology , Receptors, Thrombin/antagonists & inhibitors , Spectrometry, Mass, Fast Atom Bombardment , Tumor Cells, Cultured
5.
J Nat Prod ; 62(11): 1554-7, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10579872

ABSTRACT

A series of phospholipids, including previously undescribed compounds 4-7, were isolated by a bioactivity-guided fractionation from the marine sponge Spirastrella abata as inhibitors of cholesterol biosynthesis in human liver cells. These compounds were identified as lyso-PAF analogues (1-5) and lysophosphatidylcholines (6, 7) based on NMR and MS analyses. Compounds 1-7 specifically blocked the conversion of lanosterol into cholesterol in the Chang liver cell.


Subject(s)
Anticholesteremic Agents/pharmacology , Cholesterol/biosynthesis , Inflammation Mediators/pharmacology , Liver/metabolism , Lysophosphatidylcholines/pharmacology , Platelet Activating Factor/analogs & derivatives , Porifera/metabolism , Animals , Anticholesteremic Agents/isolation & purification , Cell Line , Cells, Cultured , Depression, Chemical , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology , Inflammation Mediators/chemistry , Inflammation Mediators/isolation & purification , Lanosterol/biosynthesis , Liver/drug effects , Liver/enzymology , Lovastatin/analogs & derivatives , Lovastatin/pharmacology , Lysophosphatidylcholines/chemistry , Lysophosphatidylcholines/isolation & purification , Magnetic Resonance Spectroscopy , Platelet Activating Factor/chemistry , Platelet Activating Factor/isolation & purification , Platelet Activating Factor/pharmacology , Porifera/chemistry
6.
Mol Cells ; 7(5): 630-4, 1997 Oct 31.
Article in English | MEDLINE | ID: mdl-9387150

ABSTRACT

Nucleoside diphosphate kinases (NDP kinases), products of the nm23 gene, catalyze the transfer of the terminal phosphate group of the nucleoside triphosphate to the corresponding diphosphate and may be involved in tumor metastasis suppression, development, and signal transduction. NDP kinase from various sources including human erythrocytes, rat brain tissue and E. coli strain BL21 transformed with pET3C expression plasmids containing nm23-H1 or nm23-H2, were purified in one step to homogeneity using ATP-sepharose affinity column chromatography. This method was applicable for the purification of various NDP kinases which show the same enzymatic activity and immunodetection, but have various molecular weight and quaternary structures.


Subject(s)
Chromatography, Affinity/methods , Isoenzymes/chemistry , Isoenzymes/isolation & purification , Nucleoside-Diphosphate Kinase/chemistry , Nucleoside-Diphosphate Kinase/isolation & purification , Animals , Brain/enzymology , Dictyostelium/enzymology , Drosophila/enzymology , Erythrocytes/enzymology , Humans , Isoenzymes/blood , Molecular Weight , Myxococcus/enzymology , Nucleoside-Diphosphate Kinase/blood , Protein Conformation , Rats , Sepharose/analogs & derivatives
8.
J Nat Prod ; 58(11): 1722-6, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8594149

ABSTRACT

Investigation of the cytotoxic constituents of a two-sponge association (Poecillastra sp. and Jaspis sp.) led to the isolation of pectenotoxin II [1] and psammaplin A as the active compounds. In an in vitro cell culture assay, 1 displayed very potent cytotoxic activities against human lung (A-549), colon (HT-29), and breast (MCF-7) cancer cell lines. Pectenotoxin II also exhibited selective cytotoxicity against several cell lines representing ovarian, renal, lung, colon, CNS, melanoma, and breast cancer, with differences in LC50 values between sensitive and resistant cell lines of 100-fold or more.


Subject(s)
Antineoplastic Agents/pharmacology , Disulfides , Furans/pharmacology , Phenylpropionates/pharmacology , Porifera/chemistry , Pyrans/pharmacology , Tyrosine/analogs & derivatives , Animals , Antineoplastic Agents/chemistry , Antineoplastic Agents/isolation & purification , Antiviral Agents/chemistry , Antiviral Agents/isolation & purification , Antiviral Agents/pharmacology , Drug Screening Assays, Antitumor , Furans/chemistry , Furans/isolation & purification , Humans , Macrolides , Phenylpropionates/chemistry , Phenylpropionates/isolation & purification , Pyrans/chemistry , Pyrans/isolation & purification , Spectrophotometry, Ultraviolet , Tumor Cells, Cultured
9.
Taehan Kanho ; 15(5): 54-8, 1976 Oct 25.
Article in Korean | MEDLINE | ID: mdl-1069881

Subject(s)
Burns/nursing , Child , Humans
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