저탄소 공정을 이용한 추출 기술인 초음파, 마이크로파 및 초고압 추출 공정기술의 이산화탄소 배출량(TCO2)과 얻어진 저분자 진세노사이드 총량의 상관관계를 비교하였다. 기존의 공정인 열수 추출 공정의 TCO2 배출량은 약 0.4 TCO2로 나타났다. 마이크로파 추출 공정의 경우 0.1437 Ton 당 CO2를 배출하는 것으로 확인 되었다. 또한, 초음파 추출 공정의 경우 0.0862 Ton 당 CO2를 배출하는 것을 확인 하였으며, 초고압 추출 공정의 경우 0.1014 Ton당 CO2를 배출하는 것을 확인 하였다. 저탄소 공정별 저분자 진세노사이드의 전환된 양을 측정한 결과 마이크로파 추출 공정의 경우 약 246.65% 정도 증진된 것을 확인 할 수 있었다. 또한, 초음파 공정의 약 275.71% 증진된 결과를 보였다. 초고압 추출 공정의 경우에는 약 295.21% 증진된 결과를 얻었다. 전체적으로 열수 추출 공정의 경우 얻어진 저분자 진세노사이드가 적은 반면 CO2 배출량이 매우 높은 것을 확인하였다. 반대로, 저탄소 추출 공정인 마이크로파, 초음파 및 초고압 공정의 경우 얻어진 저분자 진세노사이드의 양이 높으며, 방출되는 CO2의 양이 기존의 재래 방법보다 적은 것을 확인 하였다. 따라서, 저탄소 추출 공정인 마이크로파, 초음파, 초고압 추출 공정을 통해 인삼을 효과적으로 추출을 할 수 있으며, 친환경 저탄소 공법을 통해 CO2 발생량을 억제하여 경제적으로 천연물을 추출할 수 있을 것으로 사료된다.

Welding and manufacturing process of pipelines is mainly organized with root-pass welding and fill-pass welding. Of them, root-pass welding is very difficult to automatize, compared to normal welding, and it doesn't guarantee high welding quality. Root-pass welding quality can be represented by back-bead width and back-bead height, and there are a variety of studies to predict back-bead geometry, currently. In this study, a variety of welding experiments were carried out to optimize root-pass welding process using GMA process. Based on the experimental results, optimal welding conditions were selected after analyzing correlation between welding parameters and back-bead geometry. Then, effectiveness of empirical models developed was compared and analyzed, and optimized empirical models were finally developed for predicting back-bead by analyzing the main effect of each factor which affects back-bead geometry and their influence on interaction.

Peri-implantitis (PI) is bacteria-induced inflammatory condition which affects the alveolar bone and soft tissue around implants and may result in the loss of supporting bone. Attenuation of the P. gingivalis lipopolysaccharide (LPS)-induced inflammatory response can be a new therapeutic approach in the treatment of PI. This study was conducted to evaluate the anti-inflammatory effect of 635-nm light-emitting diode (LED) irradiation over MG63 osteoblast-like cell. Scratch was made on MG63 cells with or without LPS, then 635-nm irradiated. The expression of the cyclooxygenase-2 (COX-2) proteins was evaluated with western blot. The production of the prostaglandin E2 (PGE2) and expression of the receptor activator of nuclear factor kappa-B ligand (RANKL) and osteoprotegerin (OPG) was measured with enzyme-linked immunoassay, and the cytokine profile was evaluated with the human inflammation antibody array. Wound closure effect presented in the cells treated with LPS was observed more significantly in the cells with 635-nm irradiation than the cells without irradiation. The 635-nm irradiaiton reduced LPS-induced expression of the COX-2 and production of the PGE2. Also, 635-nm irradiation affect the expression of RANKL, OPG, and proinflammatory cytokines. These results indicate that 635-nm irradiation could reduce the alveolar bone resorption induced by LPS stimulation through the inhibition of COX-2 expression and PGE2 production, the suppression of proinflammatory cytokine, and the modulation of RANKL/OPG balance in MG63 cells.

Topoisomerases are essential enzymes involved in all processes of DNA metabolism, and their inhibitors have been identified as potential anti-cancer agents. The present study examined the effect of linoelaidic acid (C18 polyunsaturated fatty) compounds derived from Gardenia jasminoids Ellis extract on the activity of eukaryotic topoisomerases inhibition. The present study identified linoelaidic acid compounds using open column fraction, HPLC, NMR and LC/MS which have effects on cell death in oral cancer cell line, FaDu, but not in immortalized normal cell line, HaCaT. Subsequent studies revealed linoelaidic acid-induced autophagy through LC3 activation. Finally, its inhibition of topoisomerase I and selectively induction of oral cancer cell death possibly implies that linoelaidic acid can be a role as potenial agents in the prevention and therapy of oral cancer.

목 적: 근거리 주시시차와 사위를 측정하여 주시시차의 방향과 분포를 연구하고 주시시차에 영향을 미치는 주시시차곡선의 3가지 변수 값을 구하여 양안시 이상의 진단과 처방에 응용하고자 한다. 방 법 : 안질환이 없으며 사시와 약시가 없고 근거리에서 수직사위가 없는 남녀 대학생 85명을 대상으로 완전교정 후 사위 및 주시시차를 측정하였다. 근거리의 완전융합제거사위는 Modified Torington Card를 이 용하였고, 주시시차는 Wesson fixation disparity card를 이용하였다. 결 과 : 주시시차곡선 유형은 제 I유형 69.4%, 제 II유형 5.9%, 제 III유형 15.3%, 제 IV유형 9.4%로 나타 나 제 I유형, 제 III유형, 제 IV유형, 제 II유형의 순으로 많았다. 일부융합제거사위와 주시시차곡선의 기울기 가 주시시차에 영향을 많이 미치는 것으로 나타났다(p=0.000). 결 론 : 근거리 주시시차는 양안시 상태에서 버전스와 조절의 상호작용을 임상적으로 확인할 수 있으므로 양안시 이상의 진단과 처방에 유용한 변수이다.

목 적: 20.30대 청장년층을 대상으로 전난시, 각막난시, 잔여난시의 빈도 및 난시도를 측정하고 전난시와 각막난시, 각막난시와 잔여난시의 상관성을 분석하였다 방 법 : 안질환 및 전신질환이 없으며 사시와 약시가 없는 마산지역 대학생(남자 43명, 여 36명) 154안을 대상으로 전난시, 각막난시, 잔여난시도를 측정하여 분석하였다.ARK(KR-8100P, TOPCON, Japan)를 이용하여 전난시 및 각막난시를 측정하고 그에 따른 잔여난시를 얻어 각각의 빈도 및 난시도의 변화를 분석하였다. 단, 3회 측정 후 평균을 이용하였다. 결 과 : 전체난시(202안)는 직난시에서 (124안, 61.4%)로 가장 높은 빈도를 보였다. 사난시를 제외한(154안) 각막난시는 직난시에서 (147안, 95.5%), 잔여난시는 도난시에서 (119안, 77.2%)로 가장 높은 빈도를 보였다. 구면굴절이상값에 따른 난시도 분석 결과 구면굴절이상도에 따라 난시도는 비례적으로 증가하였다. 전체난시와 잔여난시는 뚜렷한 양적상관관계(r=0.53, p

Low level light therapy (LLLT) is known to accelerate the process of wound healing, bone and cartilage formation, and to decrease tissue necrosis and inflammation. It also can be applicable to acute and chronic injury or degenerative disease. Despite forty- plus years of accumulating exprerience of the clinical efficacy of LLLT, their molecular biologic evidence is not fully elucidated. The aim of this review is to explore the role of the ROS system and its molecular biologic mechanism in related with inflammatory response, anti-apoptosis and angiogenesis during LLLT. We suggest that activation of ROS system explains many (if not most) of the observed response of cells to LLLT in vitro, and is likely to play a pivotal role in the response of animals and patients to LLLT for both experimental and clinical indications and diseases.

Recurrence-metastasis status of squamous cell carcinoma of tongue is a challenging oncologic problem. This study examined the expression of E-cadherin/β-catenin cell adhesion complex in squamous cell carcinoma of the tongue through an immunohistochemical study. Twenty samples from 15 patients with squamous cell carcinoma of the tongue, who were treated at the Department of Oral and Maxillofacial Surgery, consisted of primary or recurrent tumors along with matched metastatic lymph nodes were retrieved for immunohistochemical staining and grouped based on recurrence-metastasis status.Differences in stain localization were noted in E-cadherin, β–catenin and phospho β–catenin staining between different tumor groups based on the recurrence-metastasis status. The number of phospho β-catenin stain positive cells was found to have a significant role in survival. E-cadherin confirms its role as a powerful individual differentiation indicator and the role of β-catenin specially the phospho type elicts interest

A blood test is a laboratory analysis performed on a blood sample that is usually extracted from a vein in the arm using a needle, or via fingerprick. They are used to determine physiological and biochemical states, such as disease, mineral contents, drug effectiveness, and organ function. Although the term blood test is used, most routine tests (except for most haematology) are done on plasma or serum, instead of blood cells. Main advantage of using saliva in diagnostics is easy and non invasive sample taking compared to peripheral blood. According to the study published, saliva contains more than 20 percent of the proteins found in blood. The purpose of present study is to compare biochemical enzymes in saliva and in blood serum and to evaluate the usefulness of saliva specimens instead of blood in dental clinic. The saliva from 215 healthy over 50 years of aged people lived in Dong-gu district, Gwangu city was collected and the analysis was performed by six enzyme-linked immunosorbent assays (ELISA). ELISA results were compared with blood chemistry results. The values or patterns on Alanine Aminotransperase (ALT), Aspartate Aminotransperase (AST), Cholesterol and Triglyceride in saliva were not correlated with those in blood serum. However, Albumine and γ-glutamyl transpeptidase (γ-GTP) were followed the positive relationship with blood chemistry. These result showed that detection and identification of Albumine and γ-GTP level could be established by saliva ELISA analysis, so that ELISA assay on saliva could be useful alternative to serum testing.

Diabetic patients tend to exhibit delayed bone formation and osteoblast differentiation, which results in osteopenia. Recently, numerous clinical reports suggest that 635-nm light irradiation improves bone regeneration and wound healing, and reduces pain in patients suffering from diabetes. The purpose of the present study was to test the hypothesis that 635-nm irradiation can influence bone formation by MC3T3-E1 osteoblasts cultured on high concentrations of glucose(25mmol/L D-glucose) in the presence or absence of phorbol 12-myristate 13-acetate(PMA), and to establish an in vitro pathological model of bone formation. The effect of 635-nm irradiation on bone formation was investigated using Alizarin Red S staining, and alkaline phosphatase enzyme activ ity and calcium deposition assays. In addition, gene expression of the o steogenic markers BMP-2, osterix and osteocalcin were assayed by RT-PCR. Calcium deposition by MC3T3-E1 cells was reduced in the presence of high concentrations of glucose or by PMA supplementation. However, 635-nm irradiation led to an increase in calcium deposition by MC3T3 cells, followed by increased bone mineralization. mRNA expression of BMP-2 and osterix at an early stage and of osteocalcin at a late stage was significantly upregulated by 635-nm irradiation in MC3T3-E1 cells supplemented with high concentrations of glucose. Irradiation at 635 nm increases bone mineralization in MC3T3-E1 cells cultured in vitro on high concentrations of glucose and alters osteogenic gene expression, which accelerates bone formation in hyperglycemic conditions.

Human gingival fibroblasts (hGFs) were reported to play an important role in inflammatory reactions to lipopolysaccharide (LPS) from P.gingivalis in the periodontal connective tissue. Although the biostimulatory effects of hyperbaric oxygen therapy, such as anti-inflammatory activity, have been reported, the pathological mechanism is not completely understood. This study examined the changes in the inflammatory cytokine profiles, which are produced after exposure to hyperbaric oxygen in P.gingivalis LPS-treated human gingival fibroblasts, and subsequently to examine the mitogen activated protein kinase (MAPK) pathway involved in cytokine production. Gingival fibroblasts with or without P.gingivalis LPS were exposed to hyperbaric oxygen, and the cytokine profiles in the supernatant were observed using a human inflammation antibody array. The expression of cyclooxyginase-2 (COX-2) protein, phosphorylation of extracellular signal-regulated kinase (ERK1/2), p38, and c-Jun-N-terminal kinase (JNK) MAPK by western blot analysis, and the amount of prostaglandin E2 (PGE2) in the supernatant by an enzyme-linked immunoassay were determined. COX-2 protein expression and PGE2productionwereincreasedsignificantlyintheP. gingivalis LPS-treated group, and were decreased by treating P. gingivalis LPS with hyperbaric oxygen. Treatment of P. gingivalis LPS in the gingival fibroblasts led an increase in the amount of pro-inflammatory-related cytokines interleukin-6 (IL-6) and IL-8 released, whereas hyperbaric oxygen inhibits the irrelease. Ananalysis of the MAPK signal transduction showed that hyperbaric oxygen induced a significant decrease in the level of P38 phosphorylation regardless of the presence or absence of LPS. In addition, hyperbaric oxygen promoted JNK phosphorylation, significantly in the presence of LPS. Hyperbaric oxygen can inhibit pro-inflammatory cytokines and mediate the MAPK signal pathway, and appears to be useful as an anti-inflammatory tool.

The pattern of wound healing process differs markedly according to the cell types. Gingival wounds heal more rapidly without scar, however dermal wounds show collagen laid down in thick disorganized patterns and keloid formation. This h as b een s uggested t o be d ue t o the presence of d ifferent E C M components a nd c ytokines a s well a s growth factors. The purpose of this study was to examine the differential expression of genes in connection with keloid formation in gingival fibroblasts (hGFs) and dermal fibroblasts (hDFs) in response to inflammation. In this study, we investigated the differences between hGFs and hDFs in the expression and production of cyclooxygenase (COX-2), prostaglandins E2 (PGE2), transforming growth factor (TGF)-β, collagens, matrix metalloproteinases (MMPs), and tissue inhibitors of matrix metalloproteinases (TIMPs) which play important roles in collagen deposition in wound healing. The hGFs and hDFs were primary cultured and allocated to arachidonic acid (AA) treatment group and control group. Protein and mRNA were extracted right after (0 hr) and 24 hr after AA treatment. At a defined concentration of AA in hGFs and hDFs, MTT assay was performed. The mRNA and protein expression levels of COX-2, TGF-β, collagen 1 and 3, MMP 1 and TIMP 1 were examined by Real-time PCR and Western blots. The amounts of PGE2 were measured by enzyme-linked immunosorbent assay (ELISA).The expression of COX-2 and TGF-β exhibited reduced levels in hGFs , but were increased in hDFs at 24 hr after AA treatment. Production of PGE2 was increased in hGFs and hDFs at right after AA treatment but, not changed at 24 hr after AA treatment. The protein and mRNA expression of collagen 1 and 3 were decreased in hGFs , whereas increased in hDFs at 24 hr AA treatment. Expression of MMP-1 protein was increased in hGFs at 24 hr but, was decreased in hDFs at 24 hr compared with that of control. The protein expression of TIMP-1 was decreased in hGFs but, was increased in hDFs at 24 hr compared with that of control. These observations demonstrate differential expression between gingival and dermal fibroblasts in regulation of collagenolytic capacity by extracellular matrix-associated genes in keloid formation associated with wound repair.

Candida albicans and their associated Candida species are opportunistic pathogens which exists as normal flora in the oral cavities of healthy individuals. In response to physiological changes in the host, these yeasts can become pathogenic, resulting in oral candidiasis. The rapid detection and identification of Candida species in clinical laboratories are extremely important for the management of patients with hematogenous candidiasis. The presently available culture and biochemical methods for detection and species identification of Candida are time-consuming and lack the required sensitivity and specificity. In this study, we have established a seminested PCR (snPCR) using universal and species-specific primers for detection of Candida species in saliva. The universal outer primers amplified the 3end of 5.8S ribosomal DNA (rDNA) and the 5end of 28S rDNA, including the internally transcribed spacer 2 (ITS2), generating 350- to 410-bp fragments from the four commonly encountered Candida spp., viz., C. albicans, C. tropicalis, C. glabrata, and C. parapsilosis. The saliva from 331 healthy and, over 50 years of aged people lived in Dong-gu, Gwangu city, was collected. Total DNA were extracted by Hoffman-Winston yeast total DNA prep. method and performed t he s nP CR. R esults appeared to b e negative on 292 people ( 88.2%), however, 2 6 people ( 7.9%) were p ositive Candida albicans, 6 people (1.8%) were positive Candida glabrata, 5 people (1.5%) were positive Candida tropicalis, and only 2 person (0.6%) were positive Candida parapsilosis. These result showed that detection and identification of Candida species could be established by saliva analysis, so that snPCR on saliva is useful method of diagnosis of clinical fields

최근 우리나라에서 청소년범죄에 대한 대책의 하나로서 청소년범죄자의 부모에게 부모교육프로그램을 제공할 필요성에 대한 인식이 확산되고 있으며, 더 나아가 이를 법제화하여 1호처분이나 보호관찰처분 대상자의 부모에게 교육프로그램에의 참여를 강제적인 명령 혹은 의무로 부과함으로써 저조한 프로그램 참여율을 높이고, 프로그램 운용의 효과를 높여야 한다는 요구가 증가하고 있다. 이러한 시점에서 본 연구는 우리나라의 부모교육명령제도의 모델사례로서 지적되고 있는 영국의 부모교육명령제도의 도입배경, 구체적인 내용, 실시현황, 관련 쟁점, 효과 등을 자세히 소개하고 있다. 그리고 더 나아가서 위와 같은 작업을 통해서 우리가 도입하고자 하는 제도가 어떤 맥락에서 시행되었으며, 실제로는 어떻게 운용되고, 어떤 효과를 낳는가를 비판적으로 검토해봄으로서 우리나라의 도입타당성여부를 판단해 보고 있다.