• 제목/요약/키워드: Human skin fibroblast

검색결과 229건 처리시간 0.027초

한약재복합 추출물의 인간피부섬유아세포 HS68에 대한 항노화 효과 (Antiaging Activity of Mixed Extracts from Korean Medicinal Herbs on HS68 Skin Fibroblast)

  • 신동철;김귀철;송시영;김희진;양재찬;이용화;김보애
    • 대한본초학회지
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    • 제29권2호
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    • pp.39-45
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    • 2014
  • Objectives : The purpose of this study was to investigate antiaging and antioxidant effects on cultured human skin fibroblast with 80% ethanol extracts of plants including of stem of Dendropanax morbifera, Corni fructus and Lycii Fructus. Methods : An ethanol extract of three medicinal plants including stem of Dendropanax morbifera, Corni fructus and Lycii Fructus. Extracts were assessed to determine the mechanism of antioxidant and antiaging activities. Antioxidant activity of extract was evaluated by two different assays as 2,2-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging and super oxide dismutase (SOD) like activities. These extracts were tested for cell viability on HS68 skin fibroblast by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay. We investigated the effects of Ultraviolet-B irradiation on cytotoxicity, type 1 collagen, elastin level and oxidative damage in cultured human skin fibroblast (HS68). Recently, many studies have reported that elastin is also involved in inhibiting or repairing wrinkle formation, although collagen is a major factor in the skin wrinkle formation. Results : The extracts obtained dose-dependently increased the scavenging activity on DPPH radical scavenging activity and SOD like activity. The extracts of complex herbal medicine showed low cytotoxicity as more than 100% cell viability in 100ppm/ml concentration. HS68 fibroblasts were survived 70% at 120 $mJ/cm^2$ UVB irradiation and treated tumor necrosis factor (TNF)-alpha. The levels of aging factors and cytotoxicity were decreased by ethanol extract of complex herbal medicine. Conclusions : These results suggest that ethanol extracts of complex medicinal plants of including of stem of Dendropanax morbifera, Corni fructus and Lycii Fructus may have value as the potential antioxidant and antiaging medicinal plant.

단치소요산(丹梔逍遙散)이 자외선을 조사한 피부진피세포의 활성 및 유전자발현에 미치는 영향 (Effects of Danchisoyo-san on UVB-induced Cell Damage and Gene Expression in Dermal Fibroblast)

  • 임현정;유동열
    • 대한한방부인과학회지
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    • 제24권2호
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    • pp.13-32
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    • 2011
  • Objectives: This study was performed to elucidate the effects of Danchisoyo-san (DS) on cell damage and gene expression in UVB-exposed dermal fibroblast. Methods: To demonstrate the inhibitory effects of DS on aging of the skin, we used human dermal fibroblast(F6) and UVB light(30 mJ/$cm^2$) was used to damage to dermal fibroblast. We measured the nitrite production, LDH release, and gene expression in UVB-irradiated dermal fibroblast to elucidate the actionmechanism of DS. Also, we evaluated the amount of increased PICP, TIMP-1 in dermal fibroblast. PICP, TIMP-1 concentration was measured using EIA kit, and gene expression (MMP-1, procollagen, c-fos, c-jun, NF-kB, Bcl-2, Bcl-xL, iNOS) were determined using real-time PCR. Results: 1. DS inhibited LDH-release, nitrite production in UVB-irradiated dermal fibroblast. 2. DS suppressed the gene expression of MMP-1 in UVB-irradiated dermal fibroblast. 3. DS increased the gene expression of procollagen in UVB-iradiated dermal fibroblast. 4. DS suppressed the gene expression of c-jun, c-fos, NF-kB, iNOS in UVBirradiated dermal fibroblast. 5. DS increased the gene expression of Bcl-2 in UVB-iradiated dermal fibroblast. 6. DS increased the cell proliferation of dermal fibroblast. Conclusions: From the results, we concluded DS increases the cell proliferation and collagen synthesis in dermal fibroblast. So we suggest that DS has the antiwrinkle effects.

재조합 표피성장인자가 방사선이 조사된 섬유아세포 증식에 미치는 영향 (Effects of Recombinant Human Epidermal Growth Factor on the Proliferationand Radiation Survival of Human Fibroblast Cell Lines in Vitro)

  • 김현숙;강기문;이상욱;나재범;채규영
    • Radiation Oncology Journal
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    • 제24권3호
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    • pp.179-184
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    • 2006
  • 목 적: 재조합 표피성장인자는(rhEGF) 다양한 표피와 상피 세포의 증식을 자극하는 것으로 알려져 있다. 본 연구에서는 방사선이 조사된 섬유아세포의 증식에 rhEGF의 효과를 알아보고자 하였다. 대상 및 방법: 인간에서 기원한 섬유아세포를 초대배양(primary culture)한 세포를 이용하였다. 대웅제약에서 유전자 재조합하여 대장균에서 발현하여 생산한 rhEGF를 제공 받아 사용하였다. 방사선 조사는 4 MV 선형가속기(CLINAC 600C, Varian, Palo Alto, CA, USA)를 이용하여 분당 2 Gy 내외의 선량률로 균일하게 조사하였다. 조사된 방사선량은 8 Gy이었다. 생존세포수는 trypan blue 염색법을 이용하였고, rhEGF에 의한 세포주기의 변화를 관찰하기 위하여 유세포 분석법을 시행하였다. 결 과: 4 Gy의 방사선을 조사한 후 7일째까지 생존 세포수를 trypan blue 염색법을 이용하여 측정한 결과 모든 rhEGF 농도(1.0 nM, 10 nM, 100 nM, 1,000 nM )에서 방사선 조사 단독군보다 생존세포 수가 많았다. 방사선을 조사하지 않은 섬유아세포에서 rhEGF를 10 nM처리한 후 FACS scan을 시행한 결과 세포주기 중에서 S기 비율이 증가하였다. 결 론: 방사선이 조사된 섬유아세포에서 rhEGF를 투여하면 rhEGF를 투여하지 않은 섬유아세포에 비해서 세포증식이 가속됨을 확인할 수 있었다.

사상자(Torilis Fructus)가 섬유아세포의 Procollagen 생합성과 Matrix metalloproteinase-I(MMP-1)의 활성에 미치는 영향 (Effect of Torilis Fructus on Procollagen Biosynthesis and Activity of Matrix Metalloproteinase-I(MMP-1) in Human Dermal Fibroblast)

  • 구본석;황의일;소승호;이성계;한경호;김나미
    • 생약학회지
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    • 제38권4호
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    • pp.349-353
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    • 2007
  • Skin wrinkle formations are associated with collagen synthesis and matrix metalloproteinase-I(MMP-1) activity. This study was carried out to find out skin wrinkle reducing components in Torilis Fructus. Torilis Fructus were extracted with 70% ethanol and the ethanol extracts were systematically fractionated with n-hexane, ethylacetate, n-butanol and distilled water. Among them, antiwrinkle component from n-hexane fraction was purified by several column chromatographies and HPLC, which identified as torilin by $^1H-NMR,\;^{13}C-NMR$ and ESI-MS. To determine cell viability, collagen biosynthesis and MMP-1 activity, human dermal fibroblast was treated with 1-5 ppm concentrations of Torilis Fructus extract fraction and torilin. Cell viability was showed 84-102% at all group treated with 1-5 ppm. Collagen synthesis was increased in all group, especially torilin-treated group was highest amount. Active forms of MMP-1 were decreased in all group. From these results, we consider that Torilis Fructus have several antiwrinkle components and torilin may be one of the effective components.

융복합적인 웰리스를 위한 미강추출물의 항산화 활성 (Antioxidant Activities of Rice Bran Extracts for Wellness Convergence)

  • 이재혁;박정숙
    • 디지털융복합연구
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    • 제13권2호
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    • pp.401-406
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    • 2015
  • 이 논문의 목적은 미강추출물 및 탈지미강추출물의 항산화력과 피부에 대한 안전성을 살펴보는데 목적이 있다. 미강과 탈지미강은 물과 에탄올로 추출하여 사용하였다. 미강추출물의 항산화능을 보기위해 DPPH로 유도된 free radical의 소거능에 의한 항산화 활성, 리보플라빈에 의해 유도된 Superoxide 생성 억제 활성, Xanthine Oxidase 저해활성을 측정하였으며 피부에 대한 안전성을 보기위해 인간 섬유아세포의 세포독성을 MTS방법을 통하여 살펴보았다. 본 연구결과는 미강추출물과 탈지미강추출물 중에서 특히 에탄올추출물은 탁월한 항산화력을 보였으며 인간 섬유아세포에서 세포독성 없이 안전하였다. 이상의 결과로 미강 및 탈지미강 추출물 중 에탄올 추출물은 화장품과 같은 미용산업 분야에서 기능성 소재로 활용과 스킨케어분야에 융복합 할 수 있을 것으로 사료된다.

Skin Anti-Aging Activities of Bacteriochlorophyll a from Photosynthetic Bacteria, Rhodobacter sphaeroides

  • Kim, Nam Young;Yim, Tae Bin;Lee, Hyeon Yong
    • Journal of Microbiology and Biotechnology
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    • 제25권10호
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    • pp.1589-1598
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    • 2015
  • In this work, the anti-aging skin effects of bacteriochlorophyll a isolated from Rhodobacter sphaeroides are first reported, with notably low cytotoxicity in the range of 1% to 14% in adding 0.00078 (% (w/w)) of the extracts, compared with the normal growth of both human dermal fibroblast and keratinocyte cells without any treatment as a control. The highest production of procollagen from human fibroblast cells (CCD-986sk) was observed as 221.7 ng/ml with 0.001 (% (w/w)) of bacteriochlorophyll a, whereas 150 and 200 ng/ml of procollagen production resulted from addition of 0.001 (% (w/w)) of the photosynthetic bacteria. The bacteriochlorophyll-a-induced TNF-α production increased to 63.8%, which was lower secretion from HaCaT cells than that from addition of 0.00005 (% (w/w)) of bacteriochlorophyll a. Additionally, bacteriochlorophyll a upregulated the expression of genes related to skin anti-aging (i.e., keratin 10, involucrin, transglutaminase-1, and MMPs), by up to 4-15 times those of the control. However, crude extracts from R. sphaeroides did not enhance the expression level of these genes. Bacteriochlorophyll a showed higher antioxidant activity of 63.8% in DPPH free radical scavenging than those of water, ethanol, and 70% ethanol extracts (14.0%, 57.2%, and 12.6%, respectively). It was also shown that the high antioxidant activity could be attributed to the skin anti-aging effect of bacteriochlorophyll a, although R. sphaeroides itself would not exhibit significant anti-aging activities.

A PROMISING NEW ANTI-WRINKLE INGREDIENT: Pericarpium castaneae extracts

  • Kim, Beom-Jun;Jo, Byoung-Kee;Kim, Jeong-Ha
    • 대한화장품학회지
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    • 제25권4호
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    • pp.57-63
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    • 1999
  • Pericarpium castaneae extracts have variously potent activities, such as anti-oxidative activity and free radical scavenging activity. in vivo and in vitro studies both indicate that pericarpium castaneae extracts acts as a free radical scavenger($IC_{50}:7.6{\mu}g/ml$) stronger than gallic acid($IC_{50}:12.5{\mu}g/ml$) and ellagic acid($IC_{50}:15{\mu}g/ml$) which could prevent cutaneous UV damages and skin aging. The extracts showed a good effect as a anti-oxidant($IC_{50}:50{\mu}g/ml$). It was shown that the appearance of wrinkle in human skin was reduced by topical application of pericarpium castaneae extracts. And the treatment of human skin with the extracts increased the elasticity and moisture of the skin. We investigated the effect of the pericarpium castaneae extracts on production of extracellular matrix using cultured A431 fibroblast cells. The results indicated that the extracts had no detectable effect on collagen synthesis. But synthesis of cell adhesion protein was increased by the extracts. The results suggest that increase of cell adhesion protein synthesis by pericarpium castaneae extracts has closely related to reduction of wrinkle in skin.

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A PROMISING NEW ANTI-WRINKLE INGREDIENT : Pericarpium castaneae extracts

  • Kim, Beom-Jun;Jo, Byoung-Kee;Kim, Jeong-Ha
    • 대한화장품학회:학술대회논문집
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    • 대한화장품학회 1999년도 IFSCC . ASCS 학술대회 발표 논문
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    • pp.57-64
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    • 1999
  • Pericarpium castaneae extracts have variously potent activities, such as anti-oxidative activity and free radical scavenging activity. in vivo and in vivo studies both indicate that pericarpium castaneae extracts acts as a flee radical scavenger ($IC_{50}$/: 7.6$\mu\textrm{g}$/ml) stronger than gallic acid($IC_{50}$/: 12.5$\mu\textrm{g}$/ml) and ellagic acid($IC_{50}$/: 15$\mu\textrm{g}$/ml) which could prevent cutaneous UV damages and skin aging. The extracts showed a good effect as a anti-oxidant ($IC_{50}$/: 50$\mu\textrm{g}$/ml). It was shown that the appearance of wrinkle in human skin was reduced by topical application of pericarpium castaneae extracts. And the treatment of human skin with the extracts increased the elasticity and moisture of the skin. We investigated the effect of tile pericarpium castaneae extracts on production of extracellular matrix using cultured A431 fibroblast cells. The results indicated that the extracts had no detectable effect on collagen synthesis, But synthesis of cell adhesion protein was increased by the extracts. The results suggest that increase of cell adhesion protein synthesis by pericarpium castaneae extracts has closely related to reduction of wrinkle in skin.

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사람 섬유아세포에서 UVB 조사에 대한 능소화 추출물의 항산화 효과 (Effect of Campsis grandiflora on Antioxidative Activity in UVB-irradiated Human Dermal Fibroblasts)

  • 김진화;이범천;;표형배
    • 약학회지
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    • 제49권2호
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    • pp.174-179
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    • 2005
  • The human skin is constantly exposed to environmental irritants such as ultraviolet, smoke, chemicals. Free radicals and reactive oxygen species (ROS) caused by these environmen tal facts play critical roles in cellular damage. These irritants are in themselves damaging to the skin structure but they also participate the immensely complex inflammatory reaction. The purpose of this study was to investigate the skin cell protective effect of Campsis grandiflora extract on the UVB-irradiated human dermal fibroblasts (HDFs). We tested free radical and superoxide scavenging effect in vitro. C. grandiflora extracts had potent radical scavenging effect by 82% at $100{\mu}g/ml$, respectively. For testing intracellular ROS scavenging activity the cultured HDFs were analyzed by increase in DCF fluorescence upon exposure to UVB 20 $MJ/cm^2$ after treatment of C.grandiflora extracts. The results showed that oxidation of CM-DCFDA was inhibited by C.grandiflora extracts effectively and C.grandiflora extracts has a potent free radical scavenging activity in UVB- irradiated HDFs. In ROS imaging using confocal microscope we visualized DCF fluorescence in HDFs directly. In conclusion, our results suggest that C.grandiflora can be effectively used for the prevention of UV-induced adverse skin reactions such as radical production, and skin cell damage.

EFFECT OF KOREAN BLACK SOYBEAN SEED ON THE CELLULAR PROLIFERATION AND THE PRODUCTION OF TYPE 111 COLLAGEN IN SKIN FIBROBLAST

  • Lee, Chungwoo;Hyeongbae Pyo;Youngho Cho;Park, Sungmin
    • 대한화장품학회지
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    • 제24권3호
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    • pp.31-37
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    • 1998
  • Soybeans are one of the major crops for human food resource; protein, lipid, and carbohydrate. In these days, they are widely using for cosmetics to supply phospholipid; natural surfactant. In this study we used black soybean seed in korea and observed many kinds of biochemical constituents; isoflavone, melatonin, crisantemine and calcium in ethanol extract. Also, its extract (we named it Flatonin) has been demonstrated that korean black soybean seed is able to stimulate the proliferation of NIH 373 cells and increase the production of type III collagen in NIH 373 and Malme-3 (human skin fibroblast) cells. The addition of korean black soybean to quiescent NIH 373 cells resulted in an increase of proliferation which was assayed by MTF method. The maximum effect of korean black soybean was detected in 0.4% korean black soybean treated cells which was comparable to that of 5% serum(96% of 5% serum effect). The addition of korean black soybean to NIH 373 and Malme-3 cells also increased the production of type III collagen in both cells. These results indicate that korean black soybean may enhance the repair process after injury and prevent aging processes in connective tissues.

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