• 제목/요약/키워드: in vitro cytotoxicity

검색결과 1,117건 처리시간 0.03초

산화적 스트레스로 유도된 간손상에 대한 소음인보중익기탕 열수추출물의 간세포보호효과 (The Protective Activity of Soeumin Bojungykgi-tang Water Extract Against Oxidative Stress-induced Hepato-Toxicity)

  • 손진원;정지윤;김광연;황보민;박정아;조일제;백영두;정태영;김상찬;지선영
    • 대한한의학방제학회지
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    • 제25권4호
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    • pp.509-526
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    • 2017
  • Background and objectives : Soeumin Bojungykgi-tang (seBYTE) has been used to supplement qi in Korean medicine. It has been demonstrated to possess various biological functions such as anti-cancer, anti-aging and anti-inflammatory effects. The present study evaluated the protective roles of seBYTE in hepatotoxic in vitro and in vivo model. Methods : To investigate cytoprotective effect of seBYTE, HepG2 cells were pretreated with seBYTE and then subsequently exposed to $10{\mu}m$ AA for 12 h, followed by $5{\mu}m$ iron. Cell viability was examined by MTT assay, and expression of apoptosis-related proteins was evaluated by immunoblot analysis. For responsible molecular mechanisms, ROS production, GSH contents, and mitochondrial membrane potential were measured. In addition, hepatoprotective effect of seBYTE in vivo was assessed in $CCl_4$-induced animal model. Results : seBYTE prevented AA + iron-induced cytotoxicity in concentration dependent manner. In addition, ROS production, GSH depletion, and mitochondrial dysfunction induced by AA + iron were significantly reduced by seBYTE pretreatment. Furthermore, seBYTE recovered expression of the pro-apoptotic proteins such as PARP and pro-caspase-3. In animal experiment, plasma ALT and AST levels were significantly elevated in $CCl_4$ treatment, but seBYTE significantly decreased the ALT and AST levels. Moreover, seBYTE alleviated the numbers of histological activity index, percentages of degenerative regions, degenerated hepatocytes, infiltrated inflammatory cells, nitrotyrosine- and 4-hydroxynonenal-positive cells in liver. Conclusions : These results showed that hepatoprotective effect of seBYTE against on $CCl_4$-induced hepatic damages is partly due to antioxidative and anti-apoptotic process.

Immunomodulating and Antitumor Activities of Panellus serotinus Polysaccharides

  • Kim, Jeong-Hwa;Lee, Jae-Seong;Lee, Kyung-Rim;Shim, Mi-Ja;Lee, Min-Woong;Shin, Pyung-Gyun;Cheong, Jong-Chun;Yoo, Young-Bok;Lee, Tae-Soo
    • Mycobiology
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    • 제40권3호
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    • pp.181-188
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    • 2012
  • This study was initiated in order to investigate the anticancer and immunomodulating activities of crude polysaccharides extracted in methanol, neutral saline, and hot water (hereinafter referred to as Fr. MeOH, Fr. NaCl, and Fr. HW, respectively) from the fruiting bodies of Panellus serotinus. Content of ${\beta}$-glucan and protein in Fr. MeOH, Fr. NaCl, and Fr. HW extracts of P. serotinus ranged from 22.92~28.52 g/100 g and 3.24~3.68 g/100 g, respectively. In vitro cytotoxicity tests, none of the various fractions of crude polysaccharides were cytotoxic against sarcoma 180, HT-29, NIH3T3, and RAW 264.7 cell lines at the tested concentration. Intraperitoneal injection with crude polysaccharides resulted in a life prolongation effect of 23.53~44.71% in mice previously inoculated with sarcoma 180. Treatment with Fr. HW resulted in an increase in the numbers of spleen cells by 1.3 fold at the concentration of $50{\mu}g/mL$ compared with control. Treatment with Fr. NaCl resulted in improvement of the immuno-potentiating activity of B lymphocytes by increasing the alkaline phosphatase activity by 1.4 fold, compared with control, at the concentration of $200{\mu}g/mL$. Among the three fractions, maximum nitric oxide ($13.48{\mu}M$) was recorded at $500{\mu}g/mL$ in Fr. HW. Production of tumor necrosis factor alpha, interleukin-$1{\beta}$, and interleukin-6 was significantly higher, compared to the positive control, concanavalin A, at the tested concentration. Therefore, treatment with crude polysaccharides extracted from the fruiting body of P. serotinus could result in improvement of antitumor activity.

The Effect of Glycolic Acid on Human Dermal Fibroblasts: Increased Collagen Synthesis and Inhibition of MMP-2/9

  • Park, Ki-Sook;Kim, Soo-Kyoum;Lim, Sae-Hwan;Kim, Yun-Young;Park, Young-Ju;Lee, Seung-Soo;Lee, Su-Hvun;Chang, Tae-Hyun;Son, Youna-Sook
    • 대한화장품학회:학술대회논문집
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    • 대한화장품학회 2003년도 IFSCC Conference Proceeding Book II
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    • pp.519-523
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    • 2003
  • Alpha hydroxy acid (AHA) includes a group of organic acids found in natural foods such as sugarcane (glycolic acid), milk (lactic acid), apples (malic acid) and oranges (citric acid). Earlier studies demonstrated the effect of AHAs on the skin by diminishing the adhesiveness of the corneal layer and increasing the viable epidermal thickness. Recent data suggest that AHAs have some effects on the dermal component of skin and even affect the aging process of the skin. A previous study revealed increased collagen production by treatment with glycolic acid among AHAs in vitro. However, the mechanism of the regulation of collagen production by glycolic acid was unclear. In present study, we tried to demonstrate the effect of glycolic acid on human dermal fibroblasts and to unveil the mechanism of regulation of collagen production by glycolic acid in human dermal fibroblasts: proliferation of fibroblasts and collagen synthesis and degradation by collagenases in fibroblasts. Our results suggested that glycolic acid had no effect on proliferation and cytotoxicity of adult human dermal fibroblasts. However, glycolic acid not only induced the increase of the collagen synthesis in human dermal fibroblasts at lower concentration than 0.1 % but also inhibited MMP-2 activity of human dermal fibroblast in the range between 0.01 and 0.4% and MMP-9 activity of human dermal fibroblast in the range between 0.06 and 0.09%. In summary, our results suggest that glycolic acid may increase wrinkle reduction partially by both increase in collagen synthesis and decrease in collagen degradation.

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절패모(浙貝母)의 항염 및 진해거담 효과에 대한 실험연구 (Experimental Study on Anti-inflammatory, Antitussive, and Expectoration Effects of Friltillariae Thunbergii Bulbus)

  • 김진후;양원경;이수원;유이란;김승형;박양춘
    • 대한한방내과학회지
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    • 제41권3호
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    • pp.339-349
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    • 2020
  • Objective: This study aimed to evaluate anti-inflammatory and antitussive expectoration effects of Friltillariae Thunbergii Bulbus (FTB) in a mouse model. Materials and Methods: To evaluate the anti-inflammatory effects of the FTB, we conducted in vitro experiments using RAW264.7 cells. An MTT assay and enzyme-linked immunosorbent assay (ELISA) were carried out to examine the anti-inflammatory effects of FTB. The expectorant effect on phenol red secretion, the antitussive effect on cough induced by ammonia solution, and leukocyte increased inhibition effects in acute airway inflammation in the animal model were confirmed. Results: FTB did not show cytotoxicity in the experimental group at 10, 30, 50, 100, 300, or 500 ㎍/ml and significantly inhibited the increase of NO, TNF-α and IL-6 in the experimental groups at 30, 50, 100, 300, and 500 ㎍/ml concentrations. In sputum, cough, and acute airway inflammation animal models, FTB significantly increased phenol red secretion in the 400 mg/kg administration group. FTB significantly reduced the number of coughs and significantly increased cough delay time in both 200 and 400 mg/kg dose groups. FTB decreased the white blood cell count in BALF (bronchoalveolar lavage fluid) in the 400 mg/kg administration group. Conclusion: Our study revealed that FTB elicits antitussive and expectorant effects by inhibiting inflammatory cytokines, increasing sputum secretion, suppressing cough, and reducing inflammatory cells. We concluded that FTB is a highly promising agent for respiratory tract infection with therapeutic opportunities.

In Vitro Antibacterial Effect of the Combination of Galla rhois ethanol extracts and Sodium chlorate against Intramacrophage Brucella abortus

  • Cha, Chun-Nam;Hong, Il-Hwa;Yu, Eun-Ah;Park, Eun-Kee;Yoo, Chang-Yeol;Kim, Suk;Lee, Hu Jang
    • 한국식품위생안전성학회지
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    • 제29권1호
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    • pp.67-72
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    • 2014
  • 본 연구는 오배자 에탄올 추출물 (GRE), 염소산나트륨 (SC) 그리고 오배자 에탄올 추출물과 염소산나트륨 합제 (GS)의 B. abortus에 대한 항균효과를 확인하기 위해 수행되었다. GRE, SC 그리고 GS를 B. abortus에 처리하여 배양한 후, B. abortus의 생존수를 확인하였으며, 마우스 탐식세포 내 감염된 B. abortus의 증식 억제효과를 경시별 (2, 24, 48시간)로 조사하였다. GRE, SC 그리고 GS는 각각 $400{\mu}g/mL$ 이하, 15 mM 그리고 0.6GS (GS 1, GRE $1,000{\mu}g/mL$ + SC 30 mM) 이하의 농도에서 세포독성을 나타나지 않았다. 모든 처리구에서 B. abortus의 생존율은 용량-의존적으로 현저하게 감소하는 결과를 나타내었다. 또한, GRE ($400{\mu}g/mL$), SC (15 mM) 그리고 0.5GS (GRE $500{\mu}g/mL$ + SC 15 mM)를 처리한 세포에서 배양 48시간 후에, B. abortus의 증식이 통계적으로 유의성 있게 감소하였으며 (GRE, p < 0.01; SC and 0.5GS, p < 0.001), 특히, GS를 처리한 경우, B. abortus의 세포내 증식이 GRE와 SC의 상승작용에 의한 강력한 항균효과를 나타내었다. 결론적으로, GS는 B. abortus에 대한 항균물질로서 유용할 뿐만 아니라, 식육과 우유 위생 분야에 적용할 수 있을 것으로 생각된다.

바나나 껍질 에탄올 추출물이 멜라닌 합성에 미치는 영향 (Positive Effect of Musa paradisiaca Peel Ethanolic Extract on Antioxidant Activity and Melanin Synthesis)

  • 김재련;김문무
    • 생명과학회지
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    • 제28권7호
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    • pp.802-810
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    • 2018
  • 노화란 나이가 들면서 생기는 몸의 변화로 검은 머리가 흰 머리로 변하는 백발화, 과산화 지질과 단백질로 구성되어 생성되는 검버섯, 주름 등으로 나타난다. 멜라닌은 tyrosine에서 DOPA를 거쳐 산화 중합반응에 의해 생성되는 고분자 물질로 인체 내에 존재하는 머리카락 및 피부 색을 결정한다. 이러한 멜라닌은 melanocyte에서 합성되며, 활성산소에 의해 과도하게 생성되면 노화를 일으킨다는 연구가 보고되고 있다. 본 연구의 목적은 항산화 효과 및 멜라닌 합성에 대한 바나나 껍질 추출물(MPEE)의 직접적인 효과를 밝히는 것이다. MPEE는 DPPH radical scavenging assay와 reducing power assay를 수행한 결과, 두 실험 모두 양성대조군인 vitamin C와 비슷한 항산화 활성을 나타내었다. 세포 실험에 앞서 세포 독성을 알아보기 위해 B16F1 세포에서 MTT assay를 수행하였다. MPEE는 $32{\mu}g/ml$ 이하의 농도에서 세포독성이 없는 것으로 나타났다. 또한, MPEE는 invitro에서 tyrosinase 활성과 DOPA-oxidation 뿐만 아니라 살아있는 세포에서 멜라닌 합성을 증가시켰다. 더욱이, $H_2O_2$로 세포를 노화시켜 L-DOPA 실험을 수행한 결과, MPEE는 멜라닌 합성을 증가시켰다. 단백질 수준의 발현을 위한 Western blot 분석을 수행한 결과, TRP-1, TPR-2와 SOD-2의 발현 수준은 MPEE의 존재 하에서 증가되었다. 이상의 결과는 MPEE가 항산화 소재로 멜라닌 합성을 촉진시킨다는 것을 암시하고 있다.

Calcium sulfate제재가 치주인대세포에 미치는 영향 (The effects of calcium sulfate on periodontal ligament cells)

  • 이준호;김소영;최성호;채중규;조규성
    • Journal of Periodontal and Implant Science
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    • 제28권2호
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    • pp.235-247
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    • 1998
  • Calcium sulfate has a long history of medical use as an implant material. The biocompatibiliry of the material has been clearly established. Bone ingrowth concomitant with resorption occurs rapidly with efficient conduction of bone from particle to particle. Calcium sulfate also has a potential for functioning as a good bamer membrane. The purpose of this study was to compare the biocompatibility of different types of calcium sulfate grafting materials including an expelimental calcium sulfate compound on periodontal ligament cells in vitro as a preliminary test towards the development of a more convenient and useful form of grafting material which could promote regeneration of periodontal tissue. Human periodontal ligament cells were collected from the premolar teeth extracted for orthodontic treatment. cells were cultured in a.MEM culture medium containing 20% FBS, at $37^{\circ}C$ and 100% humidity, in a 5% CO2 incubator. Cells were cultured into 96 well culture plate $1{\times}104$ cells per well with $\alpha$-MEM and incubated for 24 hours. After discarding the medium, those cells were cultured in $\alpha$-MEM contained with 10% FBS alone (control group), in medcal-grade calcium sulfate(MGCS group), in plaster(plaster group), experimental calcium sulfate paste(CS paste group) for 1, 2, 3 day respectively. And then each group was characterized by examining of the cell counting, MTI assay, collagen synthesis. The results \vere as follows. 1. In the analysis of cell proliferation by cell counting, both medical-grdde calcium sulfate group and plaster group showed no stastically significant difference at day 1, 2, 3 accept for plaster group at day 1 compared to control group, but there was stastically significant difference between CS paste group and all other groups at day 1, 2, 3(P<0.05). 2. In the analysis of cytotoxicity by MIT assay, both medical-grade calcium sJlfate group and plaster group showed no stastically significant difference compared to control group at day 1, 2, 3 but there was stastically significant difference between CS paste group and all other groups at day 1, 2, 3(P<0.OS). 3. In the analysis of collagen synthesis by immunoblotting assay, high level was detected for medical-grade calcium sulfate group and plaster group at day 1, 2, 3 compared to CS paste group. On the basis of these results, medical-grade calcium sulfate and plaster was shown to possess biocompatibility whereas the CS paste had unfavourable outcome. This observation shows a need for modification of the materials contained in calcium sulfate paste.

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Evaluation of Toxicity and Gene Expression Changes Triggered by Oxide Nanoparticles

  • Dua, Pooja;Chaudhari, Kiran N.;Lee, Chang-Han;Chaudhari, Nitin K.;Hong, Sun-Woo;Yu, Jong-Sung;Kim, So-Youn;Lee, Dong-Ki
    • Bulletin of the Korean Chemical Society
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    • 제32권6호
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    • pp.2051-2057
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    • 2011
  • Several studies have demonstrated that nanoparticles (NPs) have toxic effects on cultured cell lines, yet there are no clear data describing the overall molecular changes induced by NPs currently in use for human applications. In this study, the in vitro cytotoxicity of three oxide NPs of around 100 nm size, namely, mesoporous silica (MCM-41), iron oxide ($Fe_2O_3$-NPs), and zinc oxide (ZnO-NPs), was evaluated in the human embryonic kidney cell line HEK293. Cell viability assays demonstrated that 100 ${\mu}g/mL$ MCM-41, 100 ${\mu}g/mL$ $Fe_2O_3$, and 12.5 ${\mu}g/mL$ ZnO exhibited 20% reductions in HEK293 cell viability in 24 hrs. DNA microarray analysis was performed on cells treated with these oxide NPs and further validated by real time PCR to understand cytotoxic changes occurring at the molecular level. Microarray analysis of NP-treated cells identified a number of up- and down-regulated genes that were found to be associated with inflammation, stress, and the cell death and defense response. At both the cellular and molecular levels, the toxicity was observed in the following order: ZnO-NPs > $Fe_2O_3$-NPs > MCM-41. In conclusion, our study provides important information regarding the toxicity of these three commonly used oxide NPs, which should be useful in future biomedical applications of these nanoparticles.

꽃송이버섯(Sparassis latifolia) 추출물 소수성 분획의 항암 활성 (In vitro anti-cancer activity of hydrophobic fractions of Sparassis latifolia extract using AGS, A529, and HepG2 cell lines)

  • 최문희;한효경;이용조;조한교;신현재
    • 한국버섯학회지
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    • 제12권4호
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    • pp.304-310
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    • 2014
  • 본 실험에서는 꽃송이버섯 (Sparassis crispa, formerly S. crispa) 에탄올 추출물의 소수성 분획을 분리하고 각 분획의 DPPH 항산화 활성과 위암 (AGS), 폐암 (A529), 간암 (HepG2) 세포주를 이용한 항암 활성을 MTT assay를 통해 확인 하였다. SOCC를 사용하여 총 18개의 fraction으로 분획하였고 TLC와 세포주를 이용한 항암 활성 확인을 통하여 5개의 fraction으로 압축하였다. 항암활성이 높은 5개의 fraction은 HPLC-MS를 통해 각 분획물을 분석한 결과 항산화 활성을 보이지 않았으며 약 181.0의 분자량을 가진 물질이 지표물질로 확인되었으므로 이 물질의 화학식 동정을 위하여 추가실험이 필요하다. 세포주를 이용한 항암실험 결과 꽃송이버섯 추출물은 위암 (AGS), 폐암 (A529), 간암 (HepG2) 세포주 모두에서 양성대조군인 paclitaxel보다 낮은 세포 생존율을 보여 주었으며($IC_{50}$ value), 이것은 추후 꽃송이버섯 추출물에 포함된 항암 물질 분리 연구를 위한 기초연구 결과로서 무척 의미가 크다고 할 수 있다.

품종별 렌틸 추출물의 폴리페놀화합물 함량 및 항산화 활성 (Polyphenol Contents and Antioxidant Activities of Lentil Extracts from Different Cultivars)

  • 이소희;이승욱
    • 한국식품영양과학회지
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    • 제45권7호
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    • pp.973-979
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    • 2016
  • 본 연구에서는 렌틸을 이용한 새로운 기능성 소재의 개발에 우선하여 세계적으로 소비량이 비교적 많은 벨루가, 레드, 그린, 프렌치 렌틸을 연구 소재로 선정하고, 0.2% HCl을 함유한 메탄올을 이용하여 추출물을 제조한 후 이들의 항산화 활성을 조사하였다. 총폴리페놀과 플라보노이드 함량은 각각 27.3~30.3 mg TAE/g과 13.14~16.29 mg QUE/g으로 다양하게 나타났으며, 그중 벨루가와 레드 렌틸이 상대적으로 높은 총폴리페놀 함량을 보였다. DPPH와 ABTS 라디칼 소거 활성 및 $H_2O_2$ 소거 활성은 총폴리페놀 함량이 상대적으로 높았던 벨루가와 레드 렌틸이 다른 품종에 비해 유의적으로 높은 활성을 보였으며, 항산화 활성 및 폴리페놀함량과의 비례적 상관관계가 있음을 확인할 수 있었다. ROS 소거 활성이 가장 높았던 벨루가 렌틸을 이용하여 linoleic acid에 대한 과산화 억제 효과를 FTC법으로 조사한 결과, $62.5{\sim}500{\mu}g/mL$에서 농도 의존적으로 유의적인 산화억제효과를 보였으며 $RC_{50}$$222.76{\mu}g/mL$로 확인되었다. 또한, 벨루가 및 레드 렌틸 추출물은 산화적 스트레스 발생을 통해 간세포 손상을 유발하는 것으로 알려진 알코올의 세포독성으로부터 우수한 간세포 보호 효과를 나타내었다. 따라서 향후 추가적인 세포실험과 동물실험을 통한 렌틸의 항산화 활성 검정 및 항산화 기전에 관한 연구가 필요할 것으로 생각되며, 이를 비롯한 다양한 생리활성에 대한 연구들이 이루어진다면 기능성 소재로서 렌틸의 산업적 응용이 활발해질 것으로 기대된다.