• 제목/요약/키워드: Human plasma

검색결과 997건 처리시간 0.032초

Cytotoxicity and physical properties of tricalcium silicate-based endodontic materials

  • Jang, Young-Eun;Lee, Bin-Na;Koh, Jeong-Tae;Park, Yeong-Joon;Joo, Nam-Eok;Chang, Hoon-Sang;Hwang, In-Nam;Oh, Won-Mann;Hwang, Yun-Chan
    • Restorative Dentistry and Endodontics
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    • 제39권2호
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    • pp.89-94
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    • 2014
  • Objectives: The aim of this study was to evaluate the cytotoxicity, setting time and compressive strength of MTA and two novel tricalcium silicate-based endodontic materials, Bioaggregate (BA) and Biodentine (BD). Materials and Methods: Cytotoxicity was evaluated by using a 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-5-((phenylamino)carbonyl)-2H-tetrazolium hydroxide (XTT) assay. Measurements of 9 heavy metals (arsenic, cadmium, chromium, copper, iron, lead, manganese, nickel, and zinc) were performed by inductively coupled plasma-mass spectrometry (ICP-MS) of leachates obtained by soaking the materials in distilled water. Setting time and compressive strength tests were performed following ISO requirements. Results: BA had comparable cell viability to MTA, whereas the cell viability of BD was significantly lower than that of MTA. The ICP-MS analysis revealed that BD released significantly higher amount of 5 heavy metals (arsenic, copper, iron, manganese, and zinc) than MTA and BA. The setting time of BD was significantly shorter than that of MTA and BA, and the compressive strength of BA was significantly lower than that of MTA and BD. Conclusions: BA and BD were biocompatible, and they did not show any cytotoxic effects on human periodontal ligament fibroblasts. BA showed comparable cytotoxicity to MTA but inferior physical properties. BD had somewhat higher cytotoxicity but superior physical properties than MTA.

A549 폐 상피세포에서 합토글로빈에 의한 염증반응 조절 (Inflammatory Regulation by Haptoglobin in A549 Cells)

  • 김남훈;이명재;김인숙
    • 생명과학회지
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    • 제16권3호
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    • pp.500-504
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    • 2006
  • 합토글로빈(Hp)은 조직손상이나 감염 등의 염증시에 혈중 농도가 증가하는 급성기반응단백질로서 주로 간에서 생합성되지만 염증을 동반한 폐에서도 발현됨이 보고되었다. 폐에서 합성되는 Hp이 염증반응에 어떤 영향을 주는지를 조사하고자, Hp을 과발현하는 폐상피세포를 사용하여 COX-2 및 염증관련 cytokine들의 발현을 조사하였다. Stable transfection 또는 transient transfection된 A549 세포에서 Hp이 잘 발현되고 있음을 확인한 후 COX-2의 발현을 측정한 결과, Hp의 과발현에 의해 COX-2 합성이 현저히 증가함을 확인할 수 있었다. 또한 Hp을 과발현하는 A549세포에 LPS ($1{\mu}g/ml$) 또는 $IL-1{\beta}$ (100 U/ml)를 각각 24시간 동안 처치하였을 때, Hp에 의한 COX-2 발현 증가는 LPS또는 $IL-1{\beta}$자극에 의해 협동적으로 증가하였다. ACP-based PCR 방법으로 염증관련 cytokine들의 발현을 측정한 결과, Hp에 의해 SPARC의 발현이 현저히 저하되는 반면에 IL-4 및 S100A1 유전자 발현은 약간 증가함을 알 수 있었다. 이러한 결과들은 폐상피세포에서 Hp이 염증반응을 활성화시키는 기전으로 작용함을 시사한다.

흰쥐에서 어성초 열수 추출물을 포함한 혼합물의 숙취해소 효과 (Effect of Mixture Including Hot Water Extract of Houttuynia cordata Thunb on Ethanol-Induced Hangover in Rats)

  • 유양희;이현미;정창식;이민재;전우진
    • 한국식품영양과학회지
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    • 제45권10호
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    • pp.1508-1512
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    • 2016
  • 어성초 열수 추출물, 연잎 열수 추출물, 녹차씨 70% 에탄올 추출물의 혼합물인 MIX가 흰쥐에서 에탄올 투여에 따른 혈중 에탄올 및 아세트알데히드 농도와 에탄올 대사 효소들에 작용하는 효과와 직접적인 에탄올 대사 효소 활성에 미치는 영향을 확인하여 신규 숙취해소 소재로서 MIX의 활용 가능성을 연구하였다. 급성 에탄올을 투여한 EtOH군과 MIX-200군은 혈중 에탄올 농도가 에탄올을 투여하지 않은 NC군보다 높게 나타났고, MIX-200군은 EtOH군에 비교해 혈중 에탄올 농도가 에탄올 투여 3시간부터 감소하였고, 혈중 아세트알데히드의 농도는 에탄올 투여 1시간 이후부터 감소하였다. 에탄올과 아세트알데히드를 분해하는 효소인 ADH와 ALDH의 활성은 MIX-200군에서 EtOH군보다 높게 나타났다. 또한, MIX는 높은 alcohol dehydrogenase 및 acetaldehyde dehydrogenase 활성을 나타내었다. 따라서 MIX는 에탄올 대사 효소들의 활성 증가에 직 간접적으로 작용해 알코올 섭취 후 혈중 알코올 및 아세트알데히드를 감소시키는 숙취해소 작용을 갖는 신규 식품 소재로 사용될 수 있을 것으로 생각한다.

Morphology of RF-sputtered Mn-Coatings for Ti-29Nb-xHf Alloys after Micro-Pore Form by PEO

  • Park, Min-Gyu;Park, Seon-Yeong;Choe, Han-Cheol
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2016년도 추계학술대회 논문집
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    • pp.197-197
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    • 2016
  • Commercially pure titanium (CP Ti) and Ti-6Al-4V alloys have been widely used for biomedical applications. However, the use of the Ti-6Al-4V alloy in biomaterial is then a subject of controversy because aluminum ions and vanadium oxide have potential detrimental influence on the human body due to vanadium and aluminum. Hence, recent works showed that the synthesis of new Ti-based alloys for implant application involves more biocompatible metallic alloying element, such as, Nb, Hf, Zr and Mo. In particular, Nb and Hf are one of the most effective Ti ${\beta}-stabilizer$ and reducing the elastic modulus. Plasma electrolyte oxidation (PEO) is known as excellent method in the biocompatibility of biomaterial due to quickly coating time and controlled coating condition. The anodized oxide layer and diameter modulation of Ti alloys can be obtained function of improvement of cell adhesion. Manganese(Mn) plays very important roles in essential for normal growth and metabolism of skeletal tissue in vertebrates and can be detected as minor constituents in teeth and bone. Radio frequency(RF) magnetron sputtering in the various PVD methods has high deposition rates, high-purity films, extremely high adhesion of films, and excellent uniform layers for depositing a wide range of materials, including metals, alloys and ceramics like a hydroxyapatite. The aim of this study is to research the Mn coatings on the micro-pore formed Ti-29Nb-xHf alloys by RF-magnetron sputtering for dental applications. Ti-29Nb-xHf (x= 0, 3, 7 and 15wt%, mass fraction) alloys were prepared Ti-29Nb-xHf alloys of containing Hf up from 0 wt% to 15 wt% were melted by using a vacuum furnace. Ti-29Nb-xHf alloys were homogenized for 2 hr at $1050^{\circ}C$. Each alloy was anodized in solution containing typically 0.15 M calcium acetate monohydrate + 0.02 M calcium glycerophosphate at room temperature. A direct current power source was used for the process of anodization. Anodized alloys was prepared using 270V~300V anodization voltage at room. Mn coatings was produced by RF-magnetron sputtering system. RF power of 100W was applied to the target for 1h at room temperature. The microstructure, phase and composition of Mn coated oxide surface of Ti-29Nb-xHf alloys were examined by FE-SEM, EDS, and XRD.

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H2O2/HCl 처리한 Ti 임플란트의 생체활성 평가 (Evaluation of Bioactivity of Titanium Implant Treated with H2O2/HCl Solution)

  • 유재선;권오성;이오연;이민호;송기홍
    • 한국재료학회지
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    • 제15권5호
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    • pp.353-360
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    • 2005
  • Surface treatment play an important role in nucleating calcium phosphate deposition on surgical Ti implant. Therefore, the purpose of this study is to examine whether the precipitation of apatite on cp-Ti and Ti alloys are affected by surface modification in HCl and $H_2O_2$ solution. Specimens were then chemically treated with a solution containing 0.1 M HCl and 8.8M $H_2O_2$ at $80^{\circ}C$ for 30 mins, and subsequently heat-treated at $400^{\circ}C$ for 1 hour. All specimens were immersed in the HBSS with pH 7.4 at $36.5^{\circ}C$ for 15 days, and the surface was examined with XRD, SEM, EDX ana XPS. Also, pure Ti, Ti-6Al-4V and Ti-6Al-7Nb alloy specimens with and without surface treatment were implanted in the abdominal connective tissue of mice for 4 weeks. All specimens chemically treated with HCl and $H_2O_2$ solution have the ability to form a apatite layer in the HBSS which has inorganic ion composition similar to human blood plasma. The average thickness of the fibrous capsule surrounding the specimens implanted in the connective tissue was $38.57\;{\mu}m,\;62.27\;{\mu}m\;and\;45.64\;{\mu}m$ in the cp-Ti, Ti-6Al-4V ana Ti-6Al-7Nb alloy specimens with the chemical treatment respectively, and $52.20\;{\mu}m,\;75.62\;{\mu}m\;and\;66.56\;{\mu}m$ in the commercial specimens of cp-Ti, Ti-6Al-4V and Ti-6Al-7Nb without any treatment respectively. The results of this evaluation indicate that the chemically treated cp-Ti, Ti-6Al-4V ana Ti-6Al-7Nb alloys have better bioactivity and biocompatibility compared to the other metals tested.

항균성 Ag-30CaO·70SiO2 Gel의 MC3T3 세포적합성에 관한 연구 (Evaluate the Suitability of MC3T3 Cells to Antibacterial Ag-30CaO·70SiO2 Gel)

  • 윤금재;류재경;안응모;김윤종;김택남;노인섭;조성백
    • 한국재료학회지
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    • 제24권12호
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    • pp.671-676
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    • 2014
  • It is known that bones get damaged by accidents and aging. Since the discovery of Bioglass, various kinds of ceramics have been also found to bond to living bone; some of these ceramics are already being clinically used as bone-repairing materials. In the present study, antibacterial calcium silicate gel ($Ag-30CaO{\cdot}70SiO_2$ gel) was prepared by sol-gel method in order to control the microstructure, which is related to the dissolution rate and induction period of apatite formation in body environment. In addition, biological $Ag-30CaO{\cdot}70SiO_2$ is tested. This was done to impart antimicrobial activity to the $30CaO{\cdot}70SiO_2$. Ag ion was added during sol-gel synthesis to replace the $H_2O$ added during the making of the $30CaO{\cdot}70SiO_2$ gel, which has silver solutions of various concentration. After the sol-gel process, 1N-$HNO_3$ solution was used to wash the gel when synthesizing the gel, in order to maintain the porous structure and remove PEG, water soluble polymers. Then, the apatite forming ability of the sol-gel derived CaO-$SiO_2$ gels was investigated using simulated body fluid (SBF), which had almost the same ion concentration as that of human blood plasma. The gels were analyzed by FT-IR spectroscopy, SEM observation, XRD, and fluorescent microscopy. The apatite was successfully created even after washing the gel; apatite is present in an amorphous state, and was found to affect the concentration of the Ag ion in cells in MC3T3 live & dead assay results. From these results, it is suggested that a good material that can be used to repair defects of nature bone is $Ag-30CaO{\cdot}70SiO_2$ gel.

통영연근해역 양식산 및 자연산 어류 중의 미량금속 함량 및 안전성 평가 (Trace Metal Contents in Cultured and Wild fishes from the Coastal Area of Tongyeoung, Korea and their Safely Evaluations)

  • 최종덕;정인권
    • 한국식품위생안전성학회지
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    • 제20권4호
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    • pp.205-210
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    • 2005
  • 2003년 3월부터 2004변 2월까지 통영 인근 연안에 서식하고 있는 양식산 및 자연산 어류의 부위별 미량금속의 함량을 분석하였다. 수은은 Cold-amalgam법에 의하여 직접 측정하없고,납,카드뮴,비소,구리,크롬, 아연, 망간 등은 습식분해 후 ICP 및 AAS로 분석하였다. 미량금속별로는 수은이 양식산에서 0.031, 자연산이 0.047,납은 0.321, 0.407, 카드뮴은 0.048, 0.063, 비소는 1.006, 1.132, 구리는 0.467, 0.506, 크롬은 0.233, 0.293, 아연은 9.69, 12.20, 망간은 0.798, 0.624 mg/kg으로 각각 분석되었다. 대부분의 미량금속은 망간을 제외하고 자연산이 높은 값을 나타내고 있었다. 부위별로는 수은, 납, 카드뮴, 구리 및 아연 등은 비장에서 높은 함량을 보였고, 비소는 쓸개와 간에서, 크롬은 껍질에서, 망간은 비장과 간에서 높은 함량을 나타내었다. 통영연근해 어류 중의 미량금속 함량은 우리나라의 중금속 허용기준치 및 미국의 중금속 권고치를 초과하지 않았으며 자연함유량 수준인 것으로 판단되었다. 또한 우리나라 국민이 어류를 통하여 섭취하는 납, 수은, 카드뮴 등의 미량금속 주간 섭취량이 FAO/WHO에서 미량 금속 안전성 평가를 위하여 제시한 PTWI $6.0\∼13.0\%$로 조사되었다.

온담탕이 고혈압 백서와 인간유래 혈관내피세포주(ECV 304)에 미치는 영향 (An Experimental Study of Effect on ECV 304 Cells, Platelet Rich Plasma and Rats treated with L-NAME by Ondamtang extract)

  • 백일성;박창국;이소연;윤현덕;신오철;박치상
    • 대한한의학방제학회지
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    • 제12권2호
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    • pp.175-202
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    • 2004
  • Nitric oxide(NO) play an important role in normal and pathophysiological cells including as a messenger molecule, neurotransmitter, microbiocidal agent, or dilator of blood vessels and artheriosclerosis, hypertension, myocardial infarction, respectively. To investigate that Ondamtang in the potential contribution of the levels of nitric oxide generated by endothelial nitric oxide synthase (eNOS) and the mechanisms of protection against L-NAME, human ECV304 cells, which normally do not express eNOS, were expressed by L-NAME. L-NAME stimulated rat or cells were found to be resistant to injury and delayed death following the Ondam-tang. Inhibition of nitric oxide synthesis abolished the protective effect against L-NAME, thrombin and collagen exposure. Interestingly, such effects have bee observed during stimulation with agents such as KCl on L-NAME mediate rats, were damaged by the NOS inhibitor NG-nitro-L-arginine methyl ester (L-NAME). Cardiovascular diseases is one of the blood vessels and renin-angiotensin system dynfunction. So we studied on herbal medicine that have a relation of vessels endothelium necrosis. In Oriental Medicine, Ondam-tang has been used for disease in relation to cardiovascular system. We studied on the protection and inhibitory effects of cardiovascular diseases in L-NAME induced rat or ECV304 cell lines through the Cell morphological pattern, Tunel assay, LDH activity, heart rate, blood pressure and immunohistochemistric analysis by Ondam-tang. As the result of this study, In group, the anti-apoptosis and necrosis in the cardiovascular system have a potential capacity for prevented, protected and treating the diseases of cardiovascular system, against the necrosis of rat and ECV304 cells with eNOS and calpain expression by L-NAME is promoted.

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A case of mucolipidosis II presenting with prenatal skeletal dysplasia and severe secondary hyperparathyroidism at birth

  • Heo, Ju Sun;Choi, Ka Young;Sohn, Se Hyoung;Kim, Curie;Kim, Yoon Joo;Shin, Seung Han;Lee, Jae Myung;Lee, Juyoung;Sohn, Jin A;Lim, Byung Chan;Lee, Jin A;Choi, Chang Won;Kim, Ee-Kyung;Kim, Han-Suk;Kim, Beyong Il;Choi, Jung-Hwan
    • Clinical and Experimental Pediatrics
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    • 제55권11호
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    • pp.438-444
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    • 2012
  • Mucolipidosis II (ML II) or inclusion cell disease (I-cell disease) is a rarely occurring autosomal recessive lysosomal enzyme-targeting disease. This disease is usually found to occur in individuals aged between 6 and 12 months, with a clinical phenotype resembling that of Hurler syndrome and radiological findings resembling those of dysostosis multiplex. However, we encountered a rare case of an infant with ML II who presented with prenatal skeletal dysplasia and typical clinical features of severe secondary hyperparathyroidism at birth. A female infant was born at $37^{+1}$ weeks of gestation with a birth weight of 1,690 g (<3rd percentile). Prenatal ultrasonographic findings revealed intrauterine growth retardation and skeletal dysplasia. At birth, the patient had characteristic features of ML II, and skeletal radiographs revealed dysostosis multiplex, similar to rickets. In addition, the patient had high levels of alkaline phosphatase and parathyroid hormone, consistent with severe secondary neonatal hyperparathyroidism. The activities of ${\beta}$-D-hexosaminidase and ${\alpha}$-N-acetylglucosaminidase were moderately decreased in the leukocytes but were 5- to 10-fold higher in the plasma. Examination of a placental biopsy specimen showed foamy vacuolar changes in trophoblasts and syncytiotrophoblasts. The diagnosis of ML II was confirmed via GNPTAB genetic testing, which revealed compound heterozygosity of c.3091C>T (p.Arg1031X) and c.3456_3459dupCAAC (p.Ile1154GlnfsX3), the latter being a novel mutation. The infant was treated with vitamin D supplements but expired because of asphyxia at the age of 2 months.

1-Deoxynojirimycin Isolated from a Bacillus subtilis Stimulates Adiponectin and GLUT4 Expressions in 3T3-L1 Adipocytes

  • Lee, Seung-Min;Do, Hyun Ju;Shin, Min-Jeong;Seong, Su-Il;Hwang, Kyo Yeol;Lee, Jae Yeon;Kwon, Ohsuk;Jin, Taewon;Chung, Ji Hyung
    • Journal of Microbiology and Biotechnology
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    • 제23권5호
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    • pp.637-643
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    • 2013
  • We have demonstrated that 1-deoxynojirimycin (DNJ) isolated from Bacillus subtilis MORI could enhance the levels of adiponectin and its receptors in differentiated 3T3-L1 adipocytes, which has been shown to be effective in lowering blood glucose levels and enhancing insulin sensitivity. DNJ was not toxic to differentiated 3T3-L1 adipocytes for up to a concentration of $5{\mu}M$. In terms of expression levels of adiponectin and its receptors (AdipoR1 and AdipoR2), DNJ in concentrations as low as $0.5{\mu}M$ elevated both mRNA and protein levels of adiponectin and transcript levels of AdipoR1 and AdipoR2. In addition, DNJ increased phosphorylation of 5' adenosine monophosphate-activated protein kinase (AMPK) in a statistically significant manner. Finally, treatment with DNJ resulted in increased mRNA expression of glucose transporter 4 (GLUT4), which encodes for a glucose transporter, along with a significant increase in glucose uptake into the adipocytes based on results of a 2-deoxy-D-[$^3H$] glucose uptake assay. Our findings indicate that DNJ may greatly facilitate glucose uptake into adipose tissues by increasing the action of adiponectin via its up-regulated expression as well as its receptor genes. In addition, the glucose-lowering effects of DNJ may be achieved by an increased abundance of GLUT4 protein in the plasma membrane, as a consequence of the increased transcript levels of the GLUT4 gene and the activation of AMPK.