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1.
Aust Endod J ; 49(3): 631-640, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37697890

ABSTRACT

This study compared the accuracy of traditional endodontic access to conservative access cavities prepared with or without novel nonrestrictive endodontic access guides by operators with different levels of clinical experience without visual aids, using a three-dimensional volumetric accuracy analysis method. The accuracy of the preparations was analysed using a novel 3D volumetric analysis by calculating the intersection and volume of the actual cavities to the planned model cavities. The experienced operator significantly outperformed the inexperienced operator in the free hand groups, while accuracy of conservative access cavities prepared using the novel guides were comparable and significantly higher than the other groups (p < 0.05). The results demonstrated clinical experience enhanced endodontic preparations accuracy and that nonrestrictive guides achieve accurate conservative access cavities which are independent of the operator skill level. Additionally, the three-dimensional volumetric analysis is a consistent and objective method to judge the accuracy of guided endodontic techniques.


Subject(s)
Dental Pulp Cavity , Endodontics
2.
Int J Mol Med ; 42(5): 2763-2775, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30226571

ABSTRACT

Melicope ptelefolia has been traditionally used to treat rheumatism and fever. The present study aimed to investigate the therapeutic effect of 3,5­di­C­ß­D­glucopyranosyl phloroacetophenone (ßGP), a main component of M. ptelefolia, on rheumatoid arthritis (RA). A model of collagen­induced arthritis (CIA) was established in mice using the RAW 264.7 murine macrophage cell line and mouse embryonic fibroblasts (MEFs). The clinical scores of arthritis, swelling, histopathological findings, and micro­computed tomography in CIA mouse paws were assessed. The levels of anti­type II collagen antibody and cytokines were determined in the plasma and cell culture supernatant, respectively. Protein and gene expression levels were analyzed by western blot and reverse transcription­quantitative polymerase chain reaction analyses. ßGP significantly decreased the gross arthritic scores of CIA mice and joint swelling, and decreased articular inflammation, cartilage degradation and bone erosion. However, ßGP did not exert any effect on anti­type II collagen immunoglobulin G plasma levels or inflammatory cytokine expression in macrophages. ßGP significantly suppressed the expression of interleukin­6 and leukemia inhibitory factor and decreased the phosphorylation of signal transducer and activator of transcription 3, and expression of receptor activator of nuclear factor­κB ligand in tumor necrosis factor­α­stimulated MEFs and in CIA mouse paws. Osteoclast­related gene expression was significantly reduced in CIA mouse paws. Taken together, ßGP suppressed the development of RA by regulating the activation of synovial fibroblasts.


Subject(s)
Acetophenones/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Arthritis, Experimental/drug therapy , Arthritis, Rheumatoid/drug therapy , Fibroblasts/drug effects , Glucosides/therapeutic use , Acetophenones/chemistry , Animals , Anti-Inflammatory Agents/chemistry , Arthritis, Experimental/pathology , Arthritis, Rheumatoid/pathology , Cytokines/analysis , Fibroblasts/pathology , Glucosides/chemistry , Male , Mice , Osteoclasts/drug effects , Osteoclasts/pathology , RAW 264.7 Cells , Rutaceae/chemistry , X-Ray Microtomography
3.
Sci Total Environ ; 627: 1544-1551, 2018 Jun 15.
Article in English | MEDLINE | ID: mdl-30857115

ABSTRACT

We aimed to assess the personal radiofrequency electromagnetic field (RF-EMF) exposure levels of children and adults through their activities, with consideration to the body shadowing effect. We recruited 50 child-adult pairs, living in Seoul, Cheonan, and Ulsan, South Korea. RF-EMF measurements were performed between September and December 2016, using a portable exposure meter tailored to capture 14 Korean radiofrequency (RF) bands ranging from 87.5 to 5875MHz. The participants carried the device for 48h and kept a time-activity diary using a smartphone application in flight mode. To enhance accuracy of the exposure assessment, the body shadowing effect was compensated during the statistical analysis with the measured RF-EMF exposure. The compensation was conducted using the hybrid model that represents the decrease of the exposure level due to the body shadowing effect. A generalized linear mixed model was used to compare the RF-EMF exposure levels by subjects and activities. The arithmetic (geometric) means of the total power density were 174.9 (36.6) µW/m2 for all participants, 226.9 (44.6) for fathers, 245.4 (44.8) for mothers, and 116.2 (30.1) for children. By compensating for the body shadowing effect, the total RF-EMF exposure increased marginally, approximately 1.4 times. Each frequency band contribution to total RF-EMF exposure consisted of 76.7%, 2.4%, 9.9%, 5.0%, 3.3%, and 2.6% for downlink, uplink, WiFi, FM Radio, TV, and WiBro bands, respectively. Among the three regions, total RF-EMF exposure was highest in Seoul, and among the activities, it was highest in the metro, followed by foot/bicycle, bus/car, and outside. The contribution of base-station exposure to total RF-EMF exposure was the highest both in parents and children. Total and base-station RF-EMF exposure levels in Korea were higher than those reported in European countries.


Subject(s)
Electromagnetic Fields , Environmental Exposure/statistics & numerical data , Adult , Cell Phone , Child , Humans , Linear Models , Radio Waves , Republic of Korea , Seoul , Smartphone
4.
Bioelectromagnetics ; 38(8): 626-647, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28708936

ABSTRACT

When a personal exposure meter (PEM) is worn by a human subject, the electric-field strength measured at the PEM is affected by a body shadowing effect. In our study, a hybrid model is proposed for modeling the body shadowing effect for when the PEM is used in an outdoor environment. The hybrid model contains responses to direct and diffused waves, the factors related to the transmission path and cross-polarization discrimination, respectively. To derive the hybrid model, responses for the direct and diffused waves are measured using a human phantom in an anechoic chamber and a reverberation chamber, respectively. Responses are measured at multiple locations in an outdoor environment and compared to the responses of the hybrid model. The hybrid model response has quartiles that deviate by an average of only 2.2 dB (1.29) from the same quartiles of the outdoor responses. Such quartile deviations are significantly smaller than those of the previous model with a body shadowing effect. Bioelectromagnetics. 38:626-647, 2017. © 2017 Wiley Periodicals, Inc.


Subject(s)
Environment , Models, Biological , Radiation Exposure/analysis , Radio Waves/adverse effects , Radiometry/instrumentation , Diffusion , Humans , Phantoms, Imaging , Radiation Exposure/adverse effects
5.
J Neurosci ; 34(35): 11744-53, 2014 Aug 27.
Article in English | MEDLINE | ID: mdl-25164669

ABSTRACT

The dopamine precursor L-3,4-dihydroxyphenylalanine (L-DOPA) is widely used as a therapeutic choice for the treatment of patients with Parkinson's disease. However, the long-term use of L-DOPA leads to the development of debilitating involuntary movements, called L-DOPA-induced dyskinesia (LID). The cAMP/protein kinase A (PKA) signaling in the striatum is known to play a role in LID. However, from among the nine known adenylyl cyclases (ACs) present in the striatum, the AC that mediates LID remains unknown. To address this issue, we prepared an animal model with unilateral 6-hydroxydopamine lesions in the substantia nigra in wild-type and AC5-knock-out (KO) mice, and examined behavioral responses to short-term or long-term treatment with L-DOPA. Compared with the behavioral responses of wild-type mice, LID was profoundly reduced in AC5-KO mice. The behavioral protection of long-term treatment with L-DOPA in AC5-KO mice was preceded by a decrease in the phosphorylation levels of PKA substrates ERK (extracellular signal-regulated kinase) 1/2, MSK1 (mitogen- and stress-activated protein kinase 1), and histone H3, levels of which were all increased in the lesioned striatum of wild-type mice. Consistently, FosB/ΔFosB expression, which was induced by long-term L-DOPA treatment in the lesioned striatum, was also decreased in AC5-KO mice. Moreover, suppression of AC5 in the dorsal striatum with lentivirus-shRNA-AC5 was sufficient to attenuate LID, suggesting that the AC5-regulated signaling cascade in the striatum mediates LID. These results identify the AC5/cAMP system in the dorsal striatum as a therapeutic target for the treatment of LID in patients with Parkinson's disease.


Subject(s)
Adenylyl Cyclase Inhibitors , Antiparkinson Agents/adverse effects , Dyskinesia, Drug-Induced/enzymology , Levodopa/adverse effects , Parkinsonian Disorders/metabolism , Adenylyl Cyclases , Animals , Blotting, Western , Disease Models, Animal , Dyskinesia, Drug-Induced/prevention & control , Immunohistochemistry , Mice , Mice, Inbred C57BL , Mice, Knockout , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction
6.
Opt Express ; 22(8): 8919-27, 2014 Apr 21.
Article in English | MEDLINE | ID: mdl-24787781

ABSTRACT

In this study, we propose new fusion technology to overcome the limitations of the current printing process for printed electronics. The combinative slot-die coating and laser direct writing on a roll-to-roll (R2R) basis was studied and applied to the fabrication of piezoresistive strain gauges. Piezoresistive sensors were fabricated for the first time by this developed fusion technology. A parametric study was performed for the R2R process, followed by a comparison of the fabricated functional devices with commercial products, which confirmed a 40% increase in the gauge factor of the fabricated sensors over the commercial product. The combinative manufacturing process for functional device fabrication will open a new chapter in the future of printed electronics due to its large area capacity at low cost.

7.
Ann Nutr Metab ; 58(3): 224-31, 2011.
Article in English | MEDLINE | ID: mdl-21811061

ABSTRACT

AIMS: This study was carried out to evaluate the hepatoprotective effect of Platycodon grandiflorum (PG) in ethanol (EtOH)-induced liver damage. METHODS AND RESULTS: PG treatment (both the total extract and saponin fraction) significantly blocked EtOH-induced oxidative stress through the preservation of activities of antioxidant enzymes in HepG2 cells. Furthermore, while the administration of EtOH to C57BL/6 mice for 6 weeks induced liver damage, along with a significant increase in plasma glutamic oxalacetic transaminase, glutamic pyruvic transaminase, hepatic triglyceride and thiobarbituric acid reactive substance levels, PG treatment significantly decreased glutamic oxalacetic transaminase, glutamic pyruvic transaminase, hepatic triglyceride and thiobarbituric acid reactive substance levels compared with the EtOH-treated control group (p < 0.05). Histological observation by hematoxylin-eosin and oil red O staining in the liver showed more effective inhibition of lipid accumulation in PG-treated groups, as compared to the EtOH-treated control group. Additionally, PG treatments appeared to enhance the activities of superoxide dismutase and catalase in the liver (p < 0.05). CONCLUSION: These results suggest that PG has a protective effect against EtOH-induced oxidative damage, possibly by inhibition of lipid accumulation and peroxidation through the enhancement of the antioxidant defense system. PG might be useful as a therapeutically potent natural ingredient for the prevention of chronic EtOH-induced oxidative stress and liver damage.


Subject(s)
Chemical and Drug Induced Liver Injury, Chronic/drug therapy , Ethanol/toxicity , Liver/drug effects , Oxidative Stress/drug effects , Plant Extracts/pharmacology , Platycodon/chemistry , Alanine Transaminase/blood , Animals , Antioxidants/pharmacology , Chemical and Drug Induced Liver Injury, Chronic/pathology , Hep G2 Cells , Humans , Lipid Peroxidation/drug effects , Liver/pathology , Male , Mice , Mice, Inbred C57BL , Thiobarbituric Acid Reactive Substances/analysis , Triglycerides/blood
8.
J Med Food ; 14(3): 209-18, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21332399

ABSTRACT

This study evaluated the anti-obesity effects of Phellinus baumii extract (PBE) in high-fat diet (HFD)-fed mice. Male 8-week-old C57BL/6 mice were randomly divided into four groups: control, normal chow diet plus vehicle; HFD-control, high-fat plus vehicle; HFD plus orlistat (Xenical(®), Roche, Basel, Switzerland) (50 mg/kg); and HFD plus PBE (500 mg/kg). PBE was administered daily by oral gavage for 12 weeks. Oral administration of PBE (500 mg/kg) significantly reduced body weight gain, hepatic lipid concentrations, and fat accumulation in epididymal adipocytes compared with mice fed HFD alone (P < .05). mRNA expression of genes related to triglyceride (TG) synthesis was suppressed in the PBE groups, and fatty acid synthase activity was also significantly inhibited (P < .05). Furthermore, we evaluated the effect of PBE on TG absorption and detected marked reduction in TG absorption in Xenical- and PBE-treated mice compared with the control group (P < .05). To determine the active compound of PBE, fractionation was conducted, and interfungin A, davallialactone, and hypholomine B were identified as the main compounds. Among the three identified compounds, as a representative compound, davallialactone was also shown to suppress fat accumulation in an in vitro model system. These anti-obesity and hypolipidemic effects appear to be partly mediated by suppressing plasma and hepatic fat accumulation through the inhibition of enzymes associated with hepatic and intestinal lipid absorption and synthesis.


Subject(s)
Anti-Obesity Agents/therapeutic use , Basidiomycota/chemistry , Biological Products/therapeutic use , Lipid Metabolism/drug effects , Obesity/prevention & control , Phytotherapy , Triglycerides/metabolism , Adipocytes/drug effects , Adipocytes/metabolism , Adipose Tissue/metabolism , Animals , Anti-Obesity Agents/pharmacology , Biological Products/pharmacology , Dietary Fats/adverse effects , Epididymis/anatomy & histology , Epididymis/drug effects , Fatty Acid Synthases/metabolism , Intestinal Absorption/drug effects , Lactones/pharmacology , Liver/drug effects , Liver/metabolism , Male , Mice , Mice, Inbred C57BL , Obesity/chemically induced , Obesity/metabolism , Orlistat , RNA, Messenger/metabolism , Random Allocation , Triglycerides/genetics , Weight Gain/drug effects
9.
Food Chem Toxicol ; 48(11): 3177-83, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20732376

ABSTRACT

The antioxidant effects of chestnut inner shell extract (CISE) were investigated in a tert-butylhydroperoxide (t-BHP)-treated HepG2 cells, and in mice that were administered carbon tetrachloride (CCl(4)) and fed a high-fat diet (HFD). Pre-incubation with CISE significantly blocked the oxidative stress induced by t-BHP treatment in HepG2 cells (P<0.05) and preserved the activities of catalase, superoxide dismutase, glutathione peroxidase, and glutathione reductase compared to group treated with t-BHP only. Similarly, the CCl(4)- and HFD-induced reduction of antioxidant enzymes activities in liver was prevented by CISE treatment compared to control groups. Furthermore, hepatic lipid peroxidation were remarkably lower (P<0.05) in the CISE-treated groups with t-BHP or HFD. To determine the active compound of CISE, the fractionation of CISE has been conducted and scoparone and scopoletin were identified as main compounds. These compounds were also shown to inhibit the t-BHP-induced ROS generation and reduction in antioxidant enzyme activity in an in vitro model system. From these results, it was demonstrated that CISE has the ability to protect against damage from oxidative stressors such as t-BHP, CCl(4) and HFD in in vitro and in vivo models. The CISE might be useful for the prevention of oxidative damage in liver cells and tissues.


Subject(s)
Antioxidants/pharmacology , Chemical and Drug Induced Liver Injury/drug therapy , Dietary Fats/adverse effects , Fagaceae/physiology , Hepatocytes/drug effects , Plant Extracts/pharmacology , Animals , Antioxidants/chemistry , Carbon Tetrachloride/toxicity , Chemical and Drug Induced Liver Injury/etiology , Chemical and Drug Induced Liver Injury/pathology , Coumarins/isolation & purification , Coumarins/pharmacology , Hep G2 Cells , Hepatocytes/enzymology , Hepatocytes/pathology , Humans , Lipid Peroxidation/drug effects , Liver/drug effects , Liver/metabolism , Liver/pathology , Male , Mice , Mice, Inbred C57BL , Nitroreductases/metabolism , Nuts/chemistry , Oxidants/toxicity , Oxidative Stress/drug effects , Plant Extracts/chemistry , Reactive Oxygen Species/metabolism , Scopoletin/isolation & purification , Scopoletin/pharmacology , Thiobarbituric Acid Reactive Substances/metabolism , tert-Butylhydroperoxide/toxicity
10.
Life Sci ; 87(13-14): 405-10, 2010 Sep 25.
Article in English | MEDLINE | ID: mdl-20723549

ABSTRACT

AIMS: this study was performed to clarify the different action mechanisms through which rosiglitazone and pioglitazone regulate lipogenesis in white adipose tissues of db/db mice, an animal model of diabetes. MAIN METHODS: male C57BLKS/J-Lepr(db/db) (db/db) mice were used for all experiments. Rosiglitazone or pioglitazone were administered once daily by oral gavage for 4 weeks at concentrations of 20mg/kg and 75 mg/kg, respectively. At 0, 3, 6, 9, 12, 15, 21, and 28 days of administration, body weights and blood glucose were determined. At the end of experiment, adiposity and gene expression were confirmed by perilipin A immunostaining and real-time PCR. KEY FINDINGS: pioglitazone treatment increased fat mass and the surface area of adipocytes more than rosiglitazone at dosages with equivalent effects on plasma glucose. Lipid parameters including plasma total cholesterol and triglycerides were decreased more in rosiglitazone-treated mice. Relative mRNA expression levels for lipid synthesis and transport including diacylglycerol acyltransferase (DGAT1/2), fatty acid translocase (CD36/FAT), fatty acid transport protein (FATP) were increased in pioglitazone-treated group compared to rosiglitazone-treated mice, but mRNA expression levels of ß-oxidation-related genes acyl-Coenzyme A dehydrogenase, very long chain (Acadvl), acyl-Coenzyme A dehydrogenase, medium chain (Acadm), and the energy expenditure-related genes triosephosphate isomerase 1 (Tpi1) and carnitine palmitoyltransferase 1b (Cpt1b) were decreased. SIGNIFICANCE: these results suggest that pioglitazone activates lipid deposition by increasing lipid synthesis and transport, but rosiglitazone stimulates ß-oxidation and energy expenditure in adipocytes of db/db mice.


Subject(s)
Adipose Tissue, White/drug effects , Diabetes Mellitus, Experimental/drug therapy , Hypoglycemic Agents/therapeutic use , Lipid Metabolism/drug effects , Thiazolidinediones/therapeutic use , Acyl-CoA Dehydrogenase/genetics , Acyl-CoA Dehydrogenase/metabolism , Adipose Tissue, White/metabolism , Animals , Blood Glucose/drug effects , Body Weight/drug effects , CD36 Antigens/genetics , CD36 Antigens/metabolism , Cholesterol/blood , Diacylglycerol O-Acyltransferase/genetics , Diacylglycerol O-Acyltransferase/metabolism , Fatty Acid Transport Proteins/genetics , Fatty Acid Transport Proteins/metabolism , Gene Expression Regulation/drug effects , Male , Mice , Mice, Inbred C57BL , Pioglitazone , Rosiglitazone , Triglycerides/blood
11.
Bioorg Med Chem Lett ; 16(3): 737-42, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16321529

ABSTRACT

A series of dinaphtho[1,2-b;2',3'-d]furan-7,12-dione derivatives were synthesized and evaluated for inhibitory activities against receptor tyrosine kinases. The naphthofuroquinone compounds with dialkylaminoethoxy group at C(5)-position (7, 8, 10, and 11) manifested strong inhibitory activities against epidermal growth factor receptor and vascular endothelial growth factor receptor. Docking study of 11 with EGFR was also performed.


Subject(s)
Enzyme Inhibitors/chemical synthesis , Furans/chemical synthesis , Naphthoquinones/chemical synthesis , Quinazolines/chemical synthesis , Receptor Protein-Tyrosine Kinases/antagonists & inhibitors , Enzyme Inhibitors/pharmacology , ErbB Receptors/antagonists & inhibitors , Furans/pharmacology , Naphthoquinones/pharmacology , Quinazolines/pharmacology , Receptors, Vascular Endothelial Growth Factor/antagonists & inhibitors , Structure-Activity Relationship
12.
Science ; 300(5618): 464-7, 2003 Apr 18.
Article in English | MEDLINE | ID: mdl-12702870

ABSTRACT

We describe a group of alloys that exhibit "super" properties, such as ultralow elastic modulus, ultrahigh strength, super elasticity, and super plasticity, at room temperature and that show Elinvar and Invar behavior. These "super" properties are attributable to a dislocation-free plastic deformation mechanism. In cold-worked alloys, this mechanism forms elastic strain fields of hierarchical structure that range in size from the nanometer scale to several tens of micrometers. The resultant elastic strain energy leads to a number of enhanced material properties.

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