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1.
Transplant Proc ; 47(2): 504-10, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25769598

ABSTRACT

BACKGROUND: There are conflicting data about the role of cardiac troponin I (cTnI) as determined by means of conventional methods for the prediction of acute rejection after heart transplantation (HT). The purpose of this study was to evaluate whether cTnI as measured by means of the early prototype high-sensitivity assay (hs-cTnI) can predict acute rejection episode after HT compared with grade of rejection in endomyocardial biopsy (EMB). METHODS: This was a single-center cross-sectional study evaluating cTnI levels with the use of both hs-cTnI and current less sensitive conventional cTnI (conv-cTnI) assays measured at the time of EMB after HT. We calculated an index ratio of observed cTnI to expected mean cTnI for each individual patient defined as the mean cTnI measurements at EMB 60 days after HT. RESULTS: A total of 252 biopsies from 47 patients were included in this study. In the multivariable mixed model analysis in relation to the presence of acute rejection 60 days after HT, hs-cTnI level was significantly related to the presence of rejection (P = .010). The hs-cTnI ratio index was significantly higher at the time of rejection (median, 1.37; interquartile range [IQR], 1.23-2.88) compared with those without rejection (median, 0.90; IQR, 0.51-1.16; P < .001). In receiver operating characteristic curve analysis, an hs-cTnI ratio index of ≥1.17 could predict the acute rejection with a sensitivity of 82.4% and a specificity of 77.1%. CONCLUSIONS: An increased hs-cTnI ratio index was significantly related to rejection episodes. Serial monitoring of hs-cTnI and comparing it with the values without rejection might be useful for the detection of acute rejection after HT.


Subject(s)
Graft Rejection/diagnosis , Heart Failure/surgery , Heart Transplantation , Troponin I/blood , Adult , Biomarkers/blood , Biopsy , Cross-Sectional Studies , Endocardium/pathology , Female , Graft Rejection/blood , Heart Failure/blood , Heart Failure/pathology , Humans , Male , Middle Aged , Predictive Value of Tests , ROC Curve , Time Factors
3.
Diabetes Metab ; 40(4): 272-7, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24630733

ABSTRACT

AIMS: This study investigated the relationship between markers of overall glucose exposure, postprandial glucose excursions and glycaemic variability in patients with type 2 diabetes mellitus (T2DM). METHODS: A total of 63 patients with T2DM (mean age 56 years) were enrolled. All wore a continuous glucose monitoring system (CGMS) device for 72 h to collect data on markers of overall glucose exposure, postprandial glucose excursions and glycaemic variability parameters. RESULTS: Spearman's correlation analysis revealed significant correlations between all markers of overall glucose exposure and various parameters related to glucose excursions. The percent coefficient of variation (CV) showed the strongest correlation with glycated albumin (r=0.470, P<0.01). In participants with HbA1c levels < 7.5% (n=33), almost all glycaemic markers and glycaemic variability parameters were significantly correlated with each other. Also, all postprandial glucose excursion parameters showed significant correlation with other glycaemic markers, and all markers of overall glucose exposure were significantly related to mean glucose, postprandial glucose excursions and glycaemic variability parameters (except CV). In contrast, in participants with HbA1c levels ≥ 7.5% (n=30), no parameters of postprandial glucose excursions and glycaemic variability were related to any markers of chronic glycaemia. CONCLUSION: Postprandial glucose excursions may explain glycaemic variability and total glucose exposures in well-controlled T2DM patients.


Subject(s)
Blood Glucose/metabolism , Diabetes Mellitus, Type 2/metabolism , Glucose/administration & dosage , Aged , Biomarkers/blood , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/drug therapy , Dietary Carbohydrates/administration & dosage , Female , Glycated Hemoglobin/metabolism , Glycation End Products, Advanced , Humans , Hypoglycemic Agents/therapeutic use , Male , Middle Aged , Postprandial Period/physiology , Serum Albumin/metabolism , Glycated Serum Albumin
5.
J Nanosci Nanotechnol ; 13(5): 3270-5, 2013 May.
Article in English | MEDLINE | ID: mdl-23858842

ABSTRACT

This paper examined the sustain and address discharge characteristics of ac-PDPs with MgO surface coated by MgO nano crystal powders. The MgO nano crystal powder was deposited by about 5% on the MgO surface by using the spray method. To investigate the effects of the partial addition of MgO nano crystal powders on the sustain discharge as well as the address discharge, the luminance, IR spectra of 823, 828 nm, cathodoluminance, and firing voltage were measured with the measurement of the address delay times and wall voltage variation in the 42-inch ac-PDP module with a high Xe content of 17%. As a result, the statistical delay characteristics were improved considerably especially under the low panel temperature of -5 degrees C for the MgO surface with MgO nano crystal powder. However, both MgO surfaces with and without the MgO nano crystal powder showed almost similar sustain and address discharge characteristics except the statistical delay characteristics.


Subject(s)
Crystallization/methods , Luminescent Measurements/methods , Magnesium Oxide/chemistry , Magnesium Oxide/radiation effects , Nanoparticles/chemistry , Nanoparticles/radiation effects , Nanotechnology/methods , Electromagnetic Fields , Light , Materials Testing , Powders
6.
Cryo Letters ; 33(1): 1-11, 2012.
Article in English | MEDLINE | ID: mdl-22434117

ABSTRACT

To identify genes that are modulated under cold-stress conditions in the earthworm Eisenia andrei, we performed a genome-wide analysis of gene expression in cold-shocked earthworms by using Serial Analysis of Gene Expression (SAGE). We identified 5,977 and 5,407 unique SAGE tags under normal and cold-stressed conditions, respectively. The majority of the SAGE tags did not match to any known expressed sequences, due to a paucity of expression data in earthworms. We converted the statistically significant SAGE tags for the cold-stressed condition into expressed sequence tags (ESTs), and the results showed that particular genes associated with energy homeostasis, cellular defense mechanisms, and ion balance were up-regulated or down-regulated. We constructed a regulatory network of some of these genes and identified rps-6 as a core gene in the cold-response regulatory-gene network. Our data provide a baseline for gene expression studies of cold shock in the Lumbricidae.


Subject(s)
Cold-Shock Response/genetics , Gene Expression Profiling , Genome , Oligochaeta/genetics , Animals , Base Sequence , Cold Temperature , Computational Biology , Energy Metabolism , Expressed Sequence Tags , Gene Expression , Gene Regulatory Networks , Genome-Wide Association Study , Ion Transport , Microarray Analysis , Oligochaeta/immunology , Oligochaeta/metabolism , Real-Time Polymerase Chain Reaction
8.
Oncogene ; 30(2): 201-11, 2011 Jan 13.
Article in English | MEDLINE | ID: mdl-20802527

ABSTRACT

Pancreatic adenocarcinoma upregulated factor (PAUF) is overproduced in certain types of cancer. However, little is known of the tumorigenic function of PAUF. In this study, we report the X-ray crystal structure of PAUF and reveal that PAUF is a mammalian lectin normally found in plant lectins. We also identify PAUF as an endogenous ligand of Toll-like receptor 2 (TLR2) and TLR4 by screening extracellular domain receptor pools. We further confirmed the specificity of the PAUF-TLR2 interaction. PAUF induces extracellular signal-regulated kinase (ERK) phosphorylation and activates the IKK-ß-mediated TPL2/MEK/ERK signaling pathway through TLR2. In agreement with the result of TLR2-mediated ERK activation by PAUF, PAUF induces increased expression of the protumorigenic cytokines RANTES and MIF in THP-1 cells. However, PAUF does not fully activate Iκ-B-α signaling pathways in THP-1 cells, and fails to translocate the p65 subunit of the nuclear factor-κB (NF-κB) complex into the nucleus, resulting in no NF-κB activation. Surprisingly, we found that PAUF also associated with the CXC chemokine receptor (CXCR4)-TLR2 complex and inhibited CXCR4-dependent, TLR2-mediated NF-κB activation. Together, these findings suggest that the new cancer-associated ligand, PAUF, may activate TLR-mediated ERK signaling to produce the protumorigenic cytokines, but inhibits TLR-mediated NF-κB signaling, thereby facilitating tumor growth and escape from innate immune surveillance.


Subject(s)
Adenocarcinoma/secondary , Lectins/metabolism , Pancreatic Neoplasms/pathology , Receptors, CXCR4/metabolism , Toll-Like Receptor 2/metabolism , Toll-Like Receptor 4/metabolism , Animals , CHO Cells , Chemokine CCL5/analysis , Chemokine CCL5/metabolism , Cricetinae , Cricetulus , Crystallography , Extracellular Signal-Regulated MAP Kinases/analysis , Extracellular Signal-Regulated MAP Kinases/metabolism , HEK293 Cells , Humans , I-kappa B Kinase/analysis , I-kappa B Kinase/metabolism , Intercellular Signaling Peptides and Proteins , Intramolecular Oxidoreductases/analysis , Intramolecular Oxidoreductases/metabolism , Lectins/chemistry , MAP Kinase Kinase Kinases/analysis , MAP Kinase Kinase Kinases/metabolism , Macrophage Migration-Inhibitory Factors/analysis , Macrophage Migration-Inhibitory Factors/metabolism , Pancreatic Neoplasms/metabolism , Phosphorylation , Protein Binding , Protein Structure, Tertiary , Proto-Oncogene Proteins/analysis , Proto-Oncogene Proteins/metabolism , Substrate Specificity , Up-Regulation
9.
Lett Appl Microbiol ; 50(5): 522-9, 2010 May.
Article in English | MEDLINE | ID: mdl-20337931

ABSTRACT

AIMS: To test degradation of malic acid content in wine by immobilized Issatchenkia orientalis KMBL 5774 cells recently isolated from Korean wine pomace as a malic acid-degrading yeast. METHODS AND RESULTS: I. orientalis KMBL 5774 cells were immobilized using a mixture of oriental oak (Quercus variabilis) charcoal with sodium alginate. When the immobilized yeast cells were observed on a scanning electron microscope, cells were efficiently immobilized on the surface area of the charcoal. A Korean wine containing a high level of malic acid was treated with the immobilized yeast cells. The HPLC analysis of the malic acid content in the treated wine showed the malic acid content was reduced to 0.75 mg ml(-1) after treatment from the original content of 8.96 mg ml(-1), representing 91.6% of the malic acid was degraded during the treatment. CONCLUSIONS: The immobilization of the malic acid-degrading yeasts with oriental oak charcoal and sodium alginate is useful for degradation of malic acid in wines containing a high level of malic acid with no significant increase in other acids. SIGNIFICANCE AND IMPACT OF THE STUDY: Malic acid is sometimes detrimental to the quality of wines when present at high concentrations in some varieties. The immobilized I. orientalis KMBL5774 cells appear to be a promising candidate in view of developing biotechnological methods for reduction of malic acid contents in wine.


Subject(s)
Industrial Microbiology , Malates/metabolism , Pichia/metabolism , Wine/microbiology , Alginates/chemistry , Cells, Immobilized/metabolism , Fermentation , Glucuronic Acid/chemistry , Hexuronic Acids/chemistry , Industrial Microbiology/instrumentation , Malates/analysis , Quercus/microbiology , Wine/analysis
10.
Oncogene ; 29(1): 56-67, 2010 Jan 07.
Article in English | MEDLINE | ID: mdl-19784070

ABSTRACT

Pancreatic cancer is characterized by early metastatic spread, but the process of tumor cell dissemination is largely unknown. In this study we show that the soluble protein pancreatic adenocarcinoma upregulated factor (PAUF) has an important role in the metastasis and progression of the disease. Variations in the level of PAUF, either by overexpression or knockdown, resulted in altered migration, invasion and proliferation capacity of pancreatic cancer cells. Moreover, depletion of PAUF in metastatic cells dramatically abrogated the spread of the cells to distant organs in an orthotopic xenograft mouse model. PAUF elicited the activation of the extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK) and AKT intracellular signaling cascades and consequently their downstream transcription factors in an autocrine manner. Genome-wide expression analysis revealed that C-X-C chemokine receptor type 4 (CXCR4) expression was induced by PAUF overexpression but was repressed by PAUF knockdown. The PAUF-mediated increase in cancer cell motility was attenuated by the CXCR4 inhibitor, AMD3100, or by anti-CXCR4 antibody. Furthermore, immunohistochemical analysis of pancreatic tumor tissues clearly showed a significant positive correlation between PAUF and CXCR4 expression. Collectively, these findings indicate that PAUF enhances the metastatic potential of pancreatic cancer cells, at least in part, by upregulating CXCR4 expression.


Subject(s)
Lectins/genetics , Pancreatic Neoplasms/pathology , Receptors, CXCR4/genetics , Up-Regulation , Animals , Benzylamines , Blotting, Western , Cell Line, Tumor , Cell Movement/drug effects , Cyclams , Extracellular Signal-Regulated MAP Kinases/metabolism , Female , Gene Expression Profiling , Gene Expression Regulation, Neoplastic , Heterocyclic Compounds/pharmacology , Humans , Immunohistochemistry , Intercellular Signaling Peptides and Proteins , Lectins/metabolism , Mice , Mice, Inbred BALB C , Mice, Nude , Neoplasm Invasiveness , Neoplasm Metastasis , Neoplasms, Experimental/genetics , Neoplasms, Experimental/metabolism , Neoplasms, Experimental/pathology , Oligonucleotide Array Sequence Analysis , Pancreatic Neoplasms/genetics , Pancreatic Neoplasms/metabolism , RNA Interference , Receptors, CXCR4/antagonists & inhibitors , Receptors, CXCR4/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Transplantation, Heterologous
11.
J Obstet Gynaecol ; 29(8): 694-7, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19821659

ABSTRACT

We assessed the pregnancy outcome of nine women inadvertently transfused with acitretin-contaminated blood products in South Korea. A total of 18 women matched to cases by age, gravidity, and singleton- or twin-pregnancy, and who were transfused with blood products not contaminated with acitretin, was also recruited. There were nine babies born in the case group. No differences (p > 0.05) were observed between cases and controls in the gestational age at delivery (38.3 +/- 1.6 weeks vs 37.8 +/- 2.2 weeks), birth weight (3,146 +/- 874 g vs 3,106 +/- 568 g), rate of pre-term deliveries (22.2% vs 11.1%) and rate of low birth weight (<2,500 g) (33.3% vs 16.7%). There was no case of malformation or neurological abnormalities born in either group. In conclusion, inadvertent exposure to acitretin-contaminated blood products was not associated with adverse pregnancy outcomes, probably because of the removal of acitretin and etretinate during the manufacturing process of blood products.


Subject(s)
Acitretin/blood , Biological Products/chemistry , Keratolytic Agents/blood , Pregnancy Outcome , Transfusion Reaction , Adult , Case-Control Studies , Drug Contamination , Female , Gestational Age , Half-Life , Humans , Infant, Newborn , Pregnancy , Psoriasis/blood , Psoriasis/drug therapy , Teratogens
12.
Int J Clin Pharmacol Ther ; 47(7): 476-82, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19640355

ABSTRACT

OBJECTIVE: Acitretin is used for the treatment of psoriasis. The purpose of this study was to validate an HPLC method for the determination of acitretin and etretinate and to investigate the pharmacokinetic characteristics of acitretin in healthy Korean subjects. MATERIALS AND METHODS: Plasma samples or calibrators were mixed with acetonitrile and retinyl acetate (internal standard). Butanol: acetonitrile (1:1 v/v) and K2HPO4 were added later. After vortexing, 30 microl of the supernatant was injected directly into the analytical column of an HPLC system. The samples were separated by C18 reversed phase HPLC and UV detection was performed at 350 nm. Various assay performances were evaluated. RESULTS: The linearity of acitretin and etretinate was adequate up to 500 ng/ml (R2 = 0.9937 for acitretin and R2 = 0.9923 for etretinate). The accuracy was 89.5 - 113.5% and the precision was satisfactory (within-run CV, 4.4 - 15.8%; between-run CV, 3.3 - 17.4%). The LLOQ was 2 ng/ml and the stability and specificity were satisfactory. However, after storage at room temperature for 24 h under light exposure, the concentrations of acitretin and etretinate decreased by 26.0 - 66.5%. Extraction recovery was 75.1 - 91.5%. Nine healthy Korean subjects were evaluated to study the pharmacokinetics of acitretin. A single oral dose of 30 mg acitretin (Neotigason, Roche Pharmaceuticals) was given to all volunteers. The mean +/- SD pharmacokinetics of acitretin in Koreans were as follows: Cmax 148.7 +/- 93.0 ng/ml, tmax 3.2 +/- 1.3 h, t1/2 81.2 +/- 26.5 h, and AUClast 2641.9 +/- 1274.8 ng h/ml. CONCLUSION: A simple HPLC method for the simultaneous determination of acitretin and etretinate was validated, and the pharmacokinetic characteristics of acitretin in the Korean population were investigated.


Subject(s)
Acitretin/blood , Etretinate/blood , Keratolytic Agents/blood , Acitretin/pharmacokinetics , Adult , Area Under Curve , Chromatography, High Pressure Liquid , Drug Stability , Drug Storage , Half-Life , Humans , Keratolytic Agents/pharmacokinetics , Male , Sensitivity and Specificity , Spectrophotometry, Ultraviolet
14.
Environ Technol ; 29(5): 497-504, 2008 May.
Article in English | MEDLINE | ID: mdl-18661733

ABSTRACT

A dairy wastewater treatment plant operates a sequencing batch reactor (SBR) and stimulates enhanced biological phosphorus removal (EBPR) process with alternating anaerobic and aerobic cycles. Occasionally, the plant suffers from a high suspended solids problem in the supernatant. Interestingly, the occurrence of high suspended solids coincided with times when the EBPR process failed to remove phosphorus. To find out if there was a relationship between the EBPR failure and the high suspended solids problem, effluent samples were collected from the site during the period of poor phosphorus removal and examined microscopically. It was found that cocci-shaped bacteria (3-4 microm in diameter) were abundant in the effluent samples and they were clustered in tetrads. These were believed to be G-bacteria and results of both Gram and Neisser staining tests were negative, suggesting that they had few intracellular polyphosphate granules. Using polymerase chain reaction (PCR), cloning and deoxyribonucleic acid (DNA) sequence analysis, the phylogenetic information of in situ G-bacteria was obtained. It was found that all of the recovered clones were clustered in the phylum of Acidobacteria.


Subject(s)
Dairying , Proteobacteria/isolation & purification , Waste Disposal, Fluid/methods , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Microscopy, Electron, Scanning , Microscopy, Phase-Contrast , Phosphorus/metabolism , Phylogeny , Polymerase Chain Reaction , Proteobacteria/genetics , Proteobacteria/growth & development , Proteobacteria/metabolism , RNA, Ribosomal, 16S/chemistry , RNA, Ribosomal, 16S/genetics , Water Pollutants, Chemical/metabolism
15.
J Appl Microbiol ; 102(5): 1401-17, 2007 May.
Article in English | MEDLINE | ID: mdl-17448175

ABSTRACT

AIMS: To obtain ammonia-oxidizing bacterial (AOB) strains inhabiting low dissolved oxygen (DO) environments and to characterize them to better understand their function and ecology. METHODS AND RESULTS: Using a serial dilution method, two AOB strains (ML1 and NL7) were isolated from chemostat reactors operated with low DO concentrations (0.12-0.24 mg l(-1)). Phylogenetically, strains ML1 and NL7 are affiliated to AOB within the Nitrosomonas europaea and Nitrosomonas oligotropha lineages, respectively. Kinetically, strain ML1 had high affinity for oxygen (0.24 +/- 0.13 mg l(-1)) and low affinity for ammonia (1.62 +/- 0.97 mg N l(-1)), while strain NL7 had high affinity for ammonia (0.48 +/- 0.35 mg l(-1)), but a surprisingly low affinity for oxygen (1.22 +/- 0.43 mg l(-1)). A co-culture experiment was used to iteratively estimate decay constants for both strains. CONCLUSIONS: The results indicated that AOB without high affinity for oxygen may have other mechanisms to persist in low DO environments, with high affinity for ammonia being important. SIGNIFICANCE AND IMPACT OF THE STUDY: This study provides a method to determine AOB growth kinetic parameters without assuming or neglecting decay constant. And, this is the first report on oxygen affinity constant of a N. oligotropha strain.


Subject(s)
Ammonia/metabolism , Nitrosomonas/classification , Oxygen/metabolism , Nitrosomonas/isolation & purification , Nitrosomonas/metabolism , Phylogeny , Polymerase Chain Reaction
16.
Oral Dis ; 13(2): 220-7, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17305626

ABSTRACT

OBJECTIVE: Temporomandibular disorder (TMD) includes a number of clinical conditions involving the masticatory musculature or the temporomandibular joint (TMJ) and associated structures. Previous studies have shown the presence of high-affinity estrogen receptors in the TMJ articular cartilage. The aim of this study was to evaluate the developmental changes in mouse TMJ under estrogen deficiency. MATERIALS AND METHODS: Four-month-old ovariectomized mice were killed after certain weeks. We examined the significant alterations of the expression patterns of bone morphogenetic protein (BMP)-4, Runx2, and bone sialoprotein (BSP) after ovariectomy. RESULTS: In the control group, BMP-4, Runx2, and BSP expressions showed no definite difference at any stage. In the ovariectomy group, the intensity of BMP-4 and Runx2 expression increased after ovariectomy. BSP immunoreactivity, however, increased slightly at 2 weeks but then decreased gradually. CONCLUSIONS: Estrogen plays important roles in the metabolism and maintenance of TMJ via regulations of signaling molecules such as BMP-4, Runx2, and BSP. Our results suggest that estrogen deficiency is a candidate cause of TMD. This study revealed further osteogenetic properties of estrogen that may be useful in the clinical treatment and prevention of TMD.


Subject(s)
Bone Morphogenetic Proteins/analysis , Core Binding Factor Alpha 1 Subunit/analysis , Ovariectomy , Temporomandibular Joint/metabolism , Animals , Bone Morphogenetic Protein 4 , Cartilage, Articular/embryology , Cartilage, Articular/metabolism , Collagen Type X/analysis , Coloring Agents , Estrogens/deficiency , Estrogens/physiology , Female , Immunohistochemistry , In Situ Hybridization , Integrin-Binding Sialoprotein , Intracellular Signaling Peptides and Proteins/analysis , Mice , Mice, Inbred ICR , Osteogenesis/physiology , Random Allocation , Sialoglycoproteins/analysis , Temporomandibular Joint/embryology , Time Factors
17.
J Cosmet Sci ; 57(4): 279-89, 2006.
Article in English | MEDLINE | ID: mdl-16957808

ABSTRACT

Matrix metalloproteinases (MMPs) are known to play an important role in photoaging by mediating the degradation of extracellular matrix proteins. To develop a new anti-aging agent for cosmetics from natural products, Melothria heterophylla (Lour.) Cogn. was selected for its antioxidant activity and inhibitory effect on expression of MMP-1 in UVA-irradiated human skin fibroblasts. Two compounds (compounds 1 and 2 ) were isolated from an ethyl acetate soluble fraction of the ethanolic extracts; they were identified as 1,2,4,6-tetra-O-galloyl-beta-(D)-glucopyranose (1) and 3,4,5-trihydroxybenzoic acid (2). These compounds were found to scavenge radicals and reactive oxygen species (ROS) and were measured to have SC50 values of 3.9 microM and 13.3 microM against 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals and values of 4.3 microM and 4.0 microM against superoxide radicals in the xanthine/xanthine oxidase system, respectively. Compounds 1 and 2 showed a dose-dependent inhibitory effect on the expression and activity of MMP-1 in UVA-induced human skin fibroblasts, but no inhibition of MMP-1 mRNA expression. Therefore, we concluded that compounds 1 and 2 significantly inhibited MMP-1 expression at the protein level. Also, these compounds were determined to have a potent antioxidant activity. From these results, we suggest that these compounds might be useful as a new anti-aging agent for photodamaged skin, but the in vitro findings must be verified in in vivo studies.


Subject(s)
Antioxidants/pharmacology , Cucurbitaceae/chemistry , Gallic Acid/pharmacology , Glucose/analogs & derivatives , Matrix Metalloproteinase Inhibitors , Skin/drug effects , Antioxidants/chemistry , Antioxidants/isolation & purification , Biphenyl Compounds/chemistry , Enzyme-Linked Immunosorbent Assay , Fibroblasts/drug effects , Fibroblasts/enzymology , Fibroblasts/radiation effects , Gallic Acid/chemistry , Gallic Acid/isolation & purification , Glucose/chemistry , Glucose/pharmacology , Humans , Hydrazines/chemistry , Matrix Metalloproteinase 1/biosynthesis , Matrix Metalloproteinase 1/genetics , Nuclear Magnetic Resonance, Biomolecular , Picrates , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Plant Roots/chemistry , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction , Skin/enzymology , Skin/radiation effects , Spectrometry, Mass, Fast Atom Bombardment , Spectrophotometry, Ultraviolet , Superoxides/chemistry
18.
J Cosmet Sci ; 57(1): 11-21, 2006.
Article in English | MEDLINE | ID: mdl-16676120

ABSTRACT

To develop a new whitening agent for cosmetics from natural products, Angelica dahurica was selected for its inhibitory effect on melanogenesis in B16 melanoma cells. From the mechanism study, it was clarified that the ethanolic extracts of this plant showed the suppression of tyrosinase synthesis but no inhibition of tyrosinase activity. In order to find the active constituents from this plant, the ethanol extracts were chromatographed repeatedly with silica gel. Two coumarin compounds were isolated from A. dahurica. Their structures were identified by physicochemical and spectral data such as UV, IR, NMR, and MS. It was shown that the active substance was isoimperatorin (10-[(3-methyl-2-butenyl)oxy]-7H-furo[3,2-g][1] benzopyran-7-one) and imperatorin (9-[(3-methyl-2-butenyl)oxy]-7H-furo[3,2-g][1] benzopyran-7-one). They significantly inhibited tyrosinase synthesis in B16 melanoma cells. To elucidate the action mechanism of the active compounds of A. dahurica, we investigated the changes in the mRNA level of tyrosinase using the RT-PCR technique. As a result, the mRNA level of tyrosinase was markedly reduced by active compounds of A. dahurica. From these results, we suggest that these extracts might be useful as a new whitening agent in cosmetics, but the in vitro findings must be verified in in vivo skin-lightening studies.


Subject(s)
Angelica/chemistry , Cosmetics , Plant Extracts/pharmacology , Skin Pigmentation/drug effects , Animals , Cell Line, Tumor , Furocoumarins/chemistry , Furocoumarins/isolation & purification , Gene Expression/drug effects , Humans , Melanins/antagonists & inhibitors , Melanins/biosynthesis , Melanoma, Experimental/drug therapy , Melanoma, Experimental/enzymology , Melanoma, Experimental/genetics , Melanoma, Experimental/metabolism , Mice , Monophenol Monooxygenase/antagonists & inhibitors , Monophenol Monooxygenase/biosynthesis , Monophenol Monooxygenase/genetics , Monophenol Monooxygenase/metabolism , Plant Extracts/chemistry , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction
19.
Int J Oral Maxillofac Surg ; 33(8): 781-5, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15556327

ABSTRACT

The mandibular symphysis is preferred as a donor site for the relatively small grafts needed for the autogeneous bone graft procedure. This study was undertaken to determine the morphology and composition of the cortical and trabecular bone in the mandibular symphyseal region using 35 mandible specimens from Koreans. The topographical patterns through the thickness of the cortical plate and the width of the trabecular bone were observed. In this study, the labial cortical plate of the mandible became thicker from the superior to the inferior aspects (P < 0.05). However, the trabecular bone width exhibited a different distribution pattern compared to the thickness of the labial cortical plate. This observation concerning the cortical and trabecular bones assists in determination of the depth of osteotomy. The results provide useful information on the mandibular symphysis graft prior to dental implant placement. These results will enable the volume of the cortical plate in the mandibular symphyseal region and its proper size, depth, and location to be predicted when removing a graft block.


Subject(s)
Bone Transplantation , Mandible/anatomy & histology , Tissue and Organ Harvesting , Alveolar Process/anatomy & histology , Cephalometry , Dental Arch/anatomy & histology , Dental Implantation, Endosseous , Humans , Mandible/surgery , Microtomy , Osteotomy/methods , Transplantation, Autologous
20.
J Biomater Sci Polym Ed ; 15(8): 1065-79, 2004.
Article in English | MEDLINE | ID: mdl-15461190

ABSTRACT

Novel water-soluble thermosensitive chitosan copolymers were prepared by graft polymerization of N-isopropylacrylamide (NIPAAm) onto chitosan using cerium ammonium nitrate (CAN) as an initiator. The physicochemical properties of the resulting chitosan-g-NIPAAm copolymers were characterized by Fourier transform infrared (FT-IR) spectroscopy, 1H-nuclear magnetic resonance, X-ray diffraction measurement, thermogravimetric analysis (TGA) and solubility test. Sol-gel transition behavior was investigated by the cloud point measurement of the chitosan-g-NIPAAm aqueous solution. The gelling temperature was examined using the vial inversion method. The percentage of grafting (%) and efficiency of grafting (%) were investigated according to concentrations of monomer and initiator. The maximum grafted chitosan copolymer was obtained with 0.4 M NIPAAm and 6 x 10(-3) M CAN. Water-soluble chitosan-g-NIPAAm copolymers were prepared successfully and they formed thermally reversible hydrogel, which exhibits a lower critical solution temperature (LCST) around 32 degrees C in aqueous solutions. A preliminary in vitro cell study showed nontoxic and biocompatible properties. These results suggest that chitosan-g-NIPAAm copolymer could be very useful in biomedical and pharmaceutical applications as an injectable material for cell and drug delivery.


Subject(s)
Biocompatible Materials/chemistry , Biocompatible Materials/chemical synthesis , Chitosan/chemistry , Polymers/chemical synthesis , Temperature , Acrylamides/chemistry , Acrylamides/toxicity , Biocompatible Materials/toxicity , Cell Survival/drug effects , Cells, Cultured , Humans , Magnetic Resonance Spectroscopy , Molecular Structure , Polymers/chemistry , Polymers/toxicity , Solubility , Spectroscopy, Fourier Transform Infrared , X-Ray Diffraction
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