• 한국식품저장유통학회지
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• 제22권5호
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• pp.751-757
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• 2015

오디 당침출액(MSE)의 산화적 스트레스 개선 효과를 확인하기 위하여 HepG2 세포에 $H_2O_2$로 산화적 스트레스를 유도시킨 다음, MSE의 보호효과를 확인하였다. MSE를 40일간 저장하여 DPPH radical scavensing을 통해 DPPH radical 소거능이 유의적으로 좋았던 저장 40일용 MSE를 선택하여 세포 실험에 적용하였다. HepG2 세포에 $500{\mu}M$ $H_2O_2$를 처리하여 산화적 스트레스를 유발시키고, MSE를 처리하여 세포 생존율을 확인한 결과, MSE 처리로 인한 세포 생존율이 유의적으로 증가하였고, ROS 생성과 과산화물에 대한 지표로 측정된 MDA 농도도 MSE 처리로 인해 효과적으로 억제되었다. 또한, $H_2O_2$ 처리로 감소된 SOD 및 CAT 활성이 MSE 처리로 인해 유의적으로 높아졌으며, $H_2O_2$를 처리로 인한 세포핵의 apoptosis body가 MSE 처리로 인해 감소함을 확인하였으며, 이는 caspase-3 활성 MSE가 억제시킴으로 인해 세포를 보호하고 있음을 확인하였다. 이상의 결과로부터 오디 당침출액은 산화적 스트레스로부터 야기되는 세포독성과 apoptosis로부터 세포 보호 효과를 확인함에 따라 향후 노화와 관련된 다양한 연구소재의 기초 자료 및 질병 예방 소재로의 가능성을 확인하였다.

• 한국식품저장유통학회지
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• 제23권7호
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• pp.1026-1032
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• 2016

시기별 병귤 추출물의 항산화 활성은 시기적으로 미숙과 시기인 9월에 가장 높았으며, 이 시기에 총 폴리페놀 함량이 가장 높았다. 특히 rutin, hesperidin, nobiletin의 함량이 높았으며, 이는 항염 활성에 영향을 미치는 것으로 여겨진다. 항염 활성에서는 NO의 생성을 억제하였으며 염증성 cytokine인 TNF-${\alpha}$의 생성 억제 활성이 가장 높았다. 또한 NO 생성을 억제하는 단백질로 알려진 iNOS 단백질의 발현 역시 억제하는 것을 확인 할 수 있었다. 항염 활성에 영향을 미칠 것으로 여겨지는 nobiletin 함량의 경우 12월에 70%이상 감소하는 것을 확인할 수 있었다. 이러한 시기별 플라보노이드 함량 분석결과는 병귤을 천연 소재로 활용하기 위한 수확시기를 확립할 수 있을 것으로 여겨진다.

• 한국식품과학회지
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• 제35권4호
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• pp.690-695
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• 2003

Phellinus ribis(찔레 영지버섯)는 약용버섯으로 일부 항암 및 관절염 치료에 사용되고 있으나 그 활성이 전혀 알려져 있지 않아 1차적으로 40% ethanol 추출물의 생리활성을 확인하였다. 항산화 활성에 있어 nitrosamine의 원인물질인 nitrite 제거활성은 pH 1.2에서 0.5 mg/mL 이하 농도에서는 50% 이하, 그리고 1 mg/mL 처리 시 $64.0{\pm}1.6%$의 제거활성을 나타냈으며, 농도 의존적으로 증가하였다. DNA 손상 및 암, 당뇨, 간경화증, 심혈관질환 등의 원인물질에 관련하여 DPPH radicals의 제거활성은 0.5 mg/mL에서 $62.5{\pm}0.3%$, 1 mg/mL 처리 시 $91.3{\pm}0.8%$로 높게 나타났다. 2.5% linoleic acid의 자동산화에 미치는 항산화 활성을 측정한 결과 0.01 mg/mL 처리 시 p<0.05 수준에서, 0.5 및 1 mg/mL에서는 p<0.001 수준에서 유의성 있게 산화를 억제하였으며, superoxide dismutase 유사활성은 $530{\pm}81\;unit/g$으로 나타났다. 그리고, 항고혈압에 관련된 angiotensin converting enzyme 저해 활성은 $12.0{\pm}1.5%$로 그 활성이 미약하였다. Human 유래 암세포에 대한 세포독성 실험결과 폐암세포인 A549의 경우 100 mg/mL 농도에서도 16%로 나타나 세포독성이 미약하였고, 자궁암 세포인 HeLa의 경우 50 mg/mL에서 45%의 효과를, 위암 세표인 AGS에서는 5 mg/mL 처리 시 24%, 50 mg/mL에서는 76%, 그리고 간암 세포주인 SK-Hep-1의 경우 50 mg/mL에서 42%의 세포독성을 나타내었다. Salmonella typhimurium TA98 및 TA100에 대한 돌연변이원성 시험결과 찔레 영지버섯 추출물은 자연복귀 집락보다 histidine revertant colony 수가 2배 이상 증가하지 않았고, 추출물의 첨가농도를 증가시켜도 histidine revertant colony 수가 증가하지 않아 돌연변이성이 없었다.

• 대한치과보철학회지
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• 제44권2호
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• pp.250-263
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• 2006

Statement of problem: Ti-alloy has been used widely since it was produced in the United States in 1947 because it has high biocompatibility and anticorrosive characteristics. Purpose: The pure titanium, however, was used limitedly due to insufficient mechanical charateristics and difficult manufacturing process. Our previous study was focused on the development of a new titanium alloy. In the previous study we found that the Ti-Ta-Nb alloy had better mechanical characteristics and similar anticorrosive characteristics to Ti-6Al-4V Material and methods: In this study, the cytotoxicity of the Ti-Ta-Nb alloy was evaluated by MTT assay using MSCs(Mesenchaimal stem cells) and L929 cells(fibroblast cell line). The biocompatibility of the Ti-Ta-Nb alloy was performed by inserting the alloy into the femur of the rabbits and observing the radiological and histological changes surrounding the alloy implant. Results: 1. In the cytotoxicity test using MSCs, the 60% survival rate was observed in pure titanium, 84% in Ti-6Al-4V alloy and 95% in Ti-10Ta-10Nb alloy. 2. In the animal study, the serial follow-up of the radiographs showed no separation or migration revealing gradual bone ingrowth surrounding the implants. Similar radiographic results were obtained among three implant groups pure titanium, Ti-6Al-4V alloy and Ti-10Ta-10Nb alloy. 3. In the histologic examination of the bone block containing the implants. the bone ingrowth was prominent around the implants with the lapse of time. There was no signs of any tissue rejection, degeneration, or inflammation. Active bone ingrowth was observed around the implants. In the comparison of the three groups, the rate of bone ingrowth was better in the Ti-10Ta-10Nb alloy group than those in pure titanium group or Ti-6Al-4V alloy group. In conclusion, Ti-10Ta-10Nb alloy revealed better biocompatibility in survival rate of the cells and bone ingrowth around the implants. Therefore we believe a newly developed Ti-10Ta-10Nb alloy can replace currently used Ti-6Al-4V alloy to increase biocompatibility and to decrease side effects. Conclusion: In conclusion, Ti-10Ta-10Nb alloy revealed better biocompatibility in survival rate of the cells and bone ingrowth around the implants. Therefore we believe a newly developed Ti-10Ta-10Nb alloy can replace currently used Ti-6Al-4V alloy to increase biocompatibility and to decrease side effects.

• 폴리머
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• 제32권6호
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• pp.516-522
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• 2008

생분해성 고분자인 poly(L-lactide-co-glycolide) (PLGA)를 이용한 조직공학용 다공성 지지체에서의 공극률, 공극의 크기, 공극의 모양 등은 주입된 세포들이 안착하여 증식하는데 있어서 중요한 요건 중 하나이다. 본 연구에서는 섬유를 세포와 다공크기와의 관계를 파악하고자 다공형성물질인 염화나트륨을 다섯 개의 범위로 분류하여 용매캐스팅/염추출법을 이용한 다양한 다공크기를 갖는 다공성 지지체를 제조하였다. (3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyltetrazolium-bromide) (MMT) 분석방법을 이용하여 제조된 지지체에 파종된 섬유륜 세포의 생존율과 증식률을 확인하였으며, in vitro 환경에서의 콜라겐 양과 DNA량을 측정하였다. In vitro 환경에의 세포간의 발생하는 여러 상호작용을 확인하기 위하여 면역결핍 쥐의 피하에 섬유륜 세포가 파종된 지지체를 이식하여 sulfated g1ycosaminoglycan(SGAG)의 합성정도와 조직학적인 평가를 수행하였다. 결론적으로 $180{\sim}250{\mu}m$ 다공크기를 갖는 지지체에서 높은 세포 생존율과 체내에서의 원할한 세포외기질의 형성을 보임으로써 여타의 지지체보다 섬유를 조직 재생에 적절할 것으로 사료된다.

• 동의생리병리학회지
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• 제33권2호
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• pp.131-140
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• 2019

The objective of present study is to evaluate concentration-dependent in vitro anti-osteoarthritic (OA) effects of synergic mixed formula consisted of dried pomegranate juice concentrate powder, Eucommiae Cortex aqueous extract and Achyranthis Radix aqueous extract 5:4:1 (g/g) mixture on the primary cultured rat articular chondrocytes. First, any cytotoxic effect of mixture was observed using MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium Bromide) assay. Next, cyto-protective effect of test substances was evaluated by using the recombinant human interleukin $(rhIL)-1{\alpha}$ induced chondrocytes. In addition, anti-inflammatory effects were also observed on the lipopolysaccaride (LPS) treated chondrocytes through prostaglandin $E_2(PGE_2)$ productions and 5-lipoxygenase (LPO) activities, and inhibitory effects on matrix metalloproteinase (MMP)-2 and MMP-9 activities were observed on $rhIL-1{\alpha}$ treated chondrocytes with their extracellular matrix (ECM) related mRNA expressions. No obvious cytotoxic effects of mixture were demonstrated. Inflammatory damages of chondrocytes and related ECM degradations induced by treatment of LPS or $rhIL-1{\alpha}$ were significantly and concentration-dependently inhibited by pretreatment of mixture from a concentration level of 0.001 mg/ml to 1 mg/ml. In addition, mixture showed $IC_{50}$ for $rhIL-1{\alpha}-induced$ MMP-2 and MMP-9 activities as 44.01 and $162.47{\mu}g/ml$, and also showed $EC_{50}$ for $rhIL-1{\alpha}-induced$ inhibition of collagen type II, SOX9 and aggrecan mRNA expression as 8.61, 10.79 and $4.47{\mu}g/ml$, respectively. It is observed that mixture showed concentration-dependent anti-inflammatory and cytoprotective ECM preserved effects on the primary cultured rat articular chondrocytes without cytotoxicity.

• Restorative Dentistry and Endodontics
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• 제45권4호
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• pp.54.1-54.16
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• 2020

Objectives: This study aimed to synthesize nanocrystals (NCs) of zinc oxide (ZnO) and calcium ion (Ca²⁺)-doped ZnO with different percentages of calcium oxide (CaO), to evaluate cytotoxicity and to assess the effects of the most promising NCs on cytotoxicity depending on lipopolysaccharide (LPS) stimulation. Materials and Methods: Nanomaterials were synthesized (ZnO and ZnO:xCa, x = 0.7; 1.0; 5.0; 9.0) and characterized using X-ray diffractometry, scanning electron microscopy, and methylene blue degradation. SAOS-2 and RAW 264.7 were treated with NCs, and evaluated for viability using the MTT assay. NCs with lower cytotoxicity were maintained in contact with LPS-stimulated (+LPS) and nonstimulated (-LPS) human dental pulp cells (hDPCs). Cell viability, nitric oxide (NO), and reactive oxygen species (ROS) production were evaluated. Cells kept in culture medium or LPS served as negative and positive controls, respectively. One-way analysis of variance and the Dunnett test (α = 0.05) were used for statistical testing. Results: ZnO:0.7Ca and ZnO:1.0Ca at 10 ㎍/mL were not cytotoxic to SAOS-2 and RAW 264.7. +LPS and -LPS hDPCs treated with ZnO, ZnO:0.7Ca, and ZnO:1.0Ca presented similar NO production to negative control (p > 0.05) and lower production compared to positive control (p < 0.05). All NCs showed reduced ROS production compared with the positive control group both in +LPS and -LPS cells (p < 0.05). Conclusions: NCs were successfully synthesized. ZnO, ZnO:0.7Ca and ZnO:1.0Ca presented the highest percentages of cell viability, decreased ROS and NO production in +LPS cells, and maintenance of NO production at basal levels.

• Restorative Dentistry and Endodontics
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• 제47권4호
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• pp.38.1-38.15
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• 2022

Objectives: This study investigated the cytotoxicity, radiopacity, pH, and dentinal tubule penetration of a paste of 1.0% calcium-doped zinc oxide nanocrystals (ZnO:1.0Ca) combined with propylene glycol (PRG) or polyethylene glycol and propylene glycol (PEG-PRG). Materials and Methods: The pastes were prepared by mixing calcium hydroxide [Ca(OH)₂] or ZnO:1.0Ca with PRG or a PEG-PRG mixture. The pH was evaluated after 24 and 96 hours of storage in deionized water. Digital radiographs were acquired for radiopacity analysis and bubble counting of each material. The materials were labeled with 0.1% fluorescein and applied to root canals, and images of their dentinal tubule penetration were obtained using confocal laser scanning microscopy. RAW264.7 macrophages were placed in different dilutions of culture media previously exposed to the materials for 24 and 96 hours and tested for cell viability using the MTT assay. Analysis of variance and the Tukey test (α = 0.05) were performed. Results: ZnO:1.0Ca materials showed lower viability at 1:1 and 1:2 dilutions than Ca(OH)₂ materials (p < 0.0001). Ca(OH)₂ had higher pH values than ZnO:1.0Ca at 24 and 96 hours, regardless of the vehicle (p < 0.05). ZnO:1.0Ca pastes showed higher radiopacity than Ca(OH)₂ pastes (p < 0.01). No between-material differences were found in bubble counting (p = 0.0902). The ZnO:1.0Ca pastes had a greater penetration depth than Ca(OH)₂ in the apical third (p < 0.0001). Conclusions: ZnO:1.0Ca medicaments presented higher penetrability, cell viability, and radiopacity than Ca(OH)₂. Higher values of cell viability and pH were present in Ca(OH)₂ than in ZnO:1.0Ca.

• 한국식품영양과학회지
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• 제40권10호
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• pp.1397-1403
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• 2011

본 연구는 삼지구엽초의 기능성 식품학적 이용성 증진을 위한 기초적인 연구로써 우리나라 산야에서 존재하며 예로부터 약용으로 이용되고 있는 삼지구엽초의 주요성분인 icariin을 분리하여 생리활성을 검토하였다. 에탄올로 추출한 삼지구엽초를 극성이 다른 용매인 에틸아세테이트, 부탄올, 헥산, 물, 클로로포름 층으로 분리하여, icariin의 함량을 측정한 결과 각각 27.9, 2.5, 1.7, 1.4, 1.3 ${\mu}g/g$이었고, icariin 수율이 가장 많은 에틸아세테이트 분획물로부터 정제한 icariin 수율은 295.5 ${\mu}g/g$이었으며 대부분 에틸아세테이트에서 용출되는 것을 확인하였다. 용매별 분획물의 항산화효과는 에틸아세테이트 분획층에서 49.0 ${\mu}g/mL$로 가장 높았으며, 부탄올(59.2 ${\mu}g/mL$), 헥산(119.8 ${\mu}g/mL$), 물(122.0 ${\mu}g/mL$), 클로로포름(138.5 ${\mu}g/mL$) 층의 순으로 나타났으며, 정제된 icariin(15.3 ${\mu}g/mL$)은 대조구인 ascorbic acid (19.5 ${\mu}g/mL$), ${\alpha}$-tocopherol(18.2 ${\mu}g/mL$)보다 다소 높은 활성을 나타내었다. Salmonella Typhimurium을 이용한 돌연변이 및 항돌연변이성에 미치는 영향을 조사한 결과, 삼지구엽초에서 분리한 icariin은 TA98과 TA100세포 모두에서 돌연변이성을 나타내지 않았다. 인간면역세포인 B세포와 T세포에서의 면역활성시험을 측정한 결과, icariin은 대조구보다 B세포에서 1.27배, T세포에서 1.28배의 비교적 높은 면역증강활성을 나타내었다. 이러한 결과는 삼지구엽초를 이용한 기능성식품 및 식품재료로서의 이용성 증진을 위한 기초 자료로 제공될 수 있을 것으로 판단된다.

• Asian Pacific Journal of Cancer Prevention
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• 제15권12호
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• pp.4773-4780
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• 2014

Background: To investigate the effects of small interference RNA (siRNA) targeting BCR/ABL mRNA on proliferation and apoptosis in the K562 human chronic myeloid leukemia (CML) cell line and to provide a theoretical rationale and experimental evidence for its potential clinical application for anti-CML treatment. Materials and Methods: The gene sequence for BCR/ABL mRNA was found from the GeneBank. The target gene site on the BCR/ABL mRNA were selected according to Max-Planck-Institute (MPI) and rational siRNA design rules, the secondary structure of the candidate targeted mRNA was predicted, the relevant thermodynamic parameters were analyzed, and the targeted gene sequences were compared with BLAST to eliminate any sequences with significant homology. Inhibition of proliferation was evaluated by MTT assay and colony-formation inhibiting test. Apoptosis was determined by flow cytometry (FCM) and the morphology of apoptotic cells was identified by Giemsa-Wright staining. Western blotting was used to analyze the expression of BCR/ABL fusion protein in K562 cells after siRNA treatment. Results: The mRNA local secondary structure calculated by RNA structure software, and the optimal design of specific siRNA were contributed by bioinformatics rules. Five sequences of BCR/ABL siRNAs were designed and synthesized in vitro. Three sequences, siRNA1384, siRNA1276 and siRNA1786, which showed the most effective inhibition of K562 cell growth, were identified among the five candidate siRNAs, with a cell proliferative inhibitory rate nearly 50% after exposure to 12.5nmol/L~50nmol/L siRNA1384 for 24,48 and 72 hours. The 50% inhibitory concentrations ($IC_{50}$) of siRNA1384, siRNA1276 and siRNA1786 for 24hours were 46.6 nmol/L, 59.3 nmol/L and 62.6 nmol/L, respectively, and 65.668 nmol/L, 76.6 nmol/L, 74.4 nmol/L for 72 hours. The colony-formation inhibiting test also indicated that, compared with control, cell growth of siRNA treated group was inhibited. FCM results showed that the rate of cell apoptosis increased 24 hours after transfecting siRNA. The results of annexinV/PI staining indicated that the rate of apoptosis imcreased (1.53%, 15.3%, 64.5%, 57.5% and 21.5%) following treamtne with siRNAs (siRNA34, siRNA372, siRNA1384, siRNA1276 and siRNA1786). Morphological analysis showed td typical morphologic changes of apoptosis such as shrunken, fragmentation nucleus as well as "apoptotic bodies" after K562 cell exposure to siRNA. Western blot analysis showed that BCR/ABL protein was reduced sharply after a single dose of 50nmol/L siRNA transfection. Conclusions: Proliferation of K562 cells was remarkbly inhibited by siRNAs (siRNA1384, siRNA1276 and siRNA1786) in a concentration-dependent manner in vitro, with effective induction of apoptosis at a concentration of 50 nmol/L. One anti-leukemia mechanism in K562 cells appeared that BCR/ABL targeted protein was highly down-regulated. The siRNAs (siRNA1384, siRNA1276 and siRNA1786) may prove valuable in the treatment of CML.