• 제목/요약/키워드: B16F1 melanoma

검색결과 329건 처리시간 0.03초

한국 자생 석곡 메탄올 추출물의 미백 및 주름개선 효과 (Whitening and Anti-wrinkle Effects of Korean Native Dendrobium moniliforme Methanol Extract)

  • 정호경;장지훈;고재형;강병만;여준환;조정희;조현우;빈철구;김성철;정원석
    • 한국약용작물학회지
    • /
    • 제22권5호
    • /
    • pp.331-338
    • /
    • 2014
  • Dendrobium moniliforme (DM) is a valuable and versatile herbal medicine with the anecdotal claims of antioxidant and anti-inflammation. In the present study, we investigated the whitening and anti-wrinkling effects of DM under various conditions with B16F10 melanoma cells and human dermal fibroblasts. The DM extract inhibited melanin contents and tyrosinase activity in a dose-dependent manner, compared with untreated group. Treatment of the DM extract effectively suppressed the ${\alpha}$-MSH-stimulated melanin formation, tyrosinase activity and dendrite outgrowth. Moreover, the ${\alpha}$-MSH-induced mRNA expressions of tyrosinase-related protein-1 (TRP-1) and tyrosinase-related protein-2 (TRP-2) and protein expression of tyrosinase were significantly attenuated by DM treatment. We also investigated the DM increased the production of type I procollagen and inhibited TNF-${\alpha}$-induced mRNA expressions of MMP-1, -3 in the human dermal fibroblast. These results indicate that DM may be a great cosmeceutical ingredient for its whitening and anti-wrinkle effects.

Synthesis and Evaluation of Coumaroyl Dipeptide Amide as Potential Whitening Agents

  • Lee, Hye-Suk;Shin, Kyong-Hoon;Ryu, Geun-Seog;Cho, In-Shik;Kim, Jae-Il;Lee, Jae-Ho;Kim, Han-Young
    • Bulletin of the Korean Chemical Society
    • /
    • 제34권10호
    • /
    • pp.3017-3021
    • /
    • 2013
  • Coumaroyl dipeptide amide, Coumaric acid-LG-$NH_2$, was prepared successfully using the solid-phase method, and its efficacy as a skin whitening agent was studied. Coumaric acid-LG-$NH_2$ was prepared with Rink-amide resin, and 96.354% of purity was obtained. Using MTT assay and LDH release assay, we found that it exhibited very low cytotoxicity. And, we found that Coumaric acid-LG-$NH_2$ inhibited tyrosinase activity dose-dependently and showed superior tyrosinase inhibitory activity to well-known whitening agent, arbutin. $IC_{50}$ value of Coumaric acid-LG-$NH_2$ was 182.4 ${\mu}M$, and $IC_{50}$ value of arbutin was 384.6 ${\mu}M$. Also, in measurement of melanin contents using B16F1 melanoma cell lines, Coumaric acid-LG-$NH_2$ reduced melanin production induced by ${\alpha}$-MSH statistically significant, and showed superior melanin inhibitory activity to p-coumaric acid or arbutin. In addition, Coumaric acid-LG-$NH_2$ reduced MC1R mRNA expression level. Thus, we concluded that MC1R pathway is the significant pathway of Coumaric acid-LG-$NH_2$, and Coumaric acid-LG-$NH_2$ has great potential to be used as novel whitening agents.

K-약침(藥鍼)의 급성(急性) 아급성(亞急性) 독성실험(毒性實驗) 및 항암효과(항암효과)에 관(關)한 실험적(實驗的) 연구(硏究) (The Study on Acute Subacute Toxicity and Anti-cancer Effect of K-herbal-acupuncture)

  • 김광호;권기록
    • 대한약침학회지
    • /
    • 제6권1호
    • /
    • pp.76-94
    • /
    • 2003
  • Objectives : The purpose of this study was to investigate Acute$\cdot$Subacute Toxicity and Anti-cancer Effect of K-Herbal-acupuncture in mice and rats. Methods : Balb/c mice were injected intraperitoneally with K-herbal-acupuncture for $LD_{50}$ and acute toxicity test. Sprague-Dawley rats were injected intraperitoneally with K-herbal-acupuncture for subacute toxicity test. K-Herbal-acupuncture was injected on abdomen of mice with S-180 cancer cell line. Result : 1. $LD_{50}$ of K-Herbal-acupuncture was limited $4{\times}10^{-3}$ml/kg~$2{\times}10^{-3}$ml/kg by the test. 2. In acute toxicity test, all of mice were down to the moving reflex, but the weight of mice was increased in treatment group, compared with the normal group. (P<0.05) 3. In acute toxicity test of serum biochemical values of mice, glucose was increased in treatment II group, total cholesterol was increased both treatments.(P<0.05) 4. In subacute toxicity test, the clinical signs of toxication was down to the moving reflex, but it is not severe like acute toxicity test, and observed weight loss at the treatments. 5. In subacute toxicity test, liver weight was decreased compared with the normal group. (P<0.05) 6. In subacute toxicity test of complete blood count test (CBC) of rat, HCT was decreased in treatments, compared with the normal group.(P<0.05) 7. In subacute toxicity test of serum biochemical values of rat, uric acid and triglyceride were decreased, and glucose was increased in treatment groups compared with the control group. (P<0.05) 8. Median survival time was increased about $45\%$ in treatment groups compared with the control group.(P<0.05) 9. Natural killer cell activity was increased in B16F10 lung cancer model, but it was not in sarcoma-180 abdomen cancer. 10. In interleukin-2 productivity test, treatment groups didn't show significant change in lung cancer and abdomen cancer, compared with the normal group.(P<0.005) 11. In making an examination of metastatic cancer with the naked eye, melanoma metastasized in the Lung of C57BL/6 mice. The treated group showed more Melanoma than the control in the numbers and volume. Conclusion : According to the result, K-herbal-acupuncture need further study to know the function and effect in cancer.

슈퍼자미(SuperC3GHi) 미강 발효물의 생리활성 (Evaluation of Biological Activities of Fermented Rice Bran from Novel Black Colored Rice Cultivar SuperC3GHi)

  • 김동주;최수민;김화영;김중학;류수노;한상준;홍성길
    • 한국작물학회지
    • /
    • 제56권4호
    • /
    • pp.420-426
    • /
    • 2011
  • 슈퍼자미(SuperC3GHi) 쌀 품종은 색소 성분인 cyanidine-3-glucoside(C3G)의 함량을 크게 증대시킨 품종이다. 슈퍼자미 벼품종을 활용한 새로운 기능성 소재 및 제품으로의 개발 가능성을 타진하기 위하여 본 연구에서는 슈퍼자미 벼품종의 버섯 균사체 발효물을 이용하여 항염증, 항알러지, 항암 기능의 검증을 수행하였다. 1. 슈퍼자미 미강 발효물의 항염 활성을 분석하기 위하여 ear-edema test를 수행한결과 약 35.6%의 염증 억제율을 나타내었다. 2. 슈퍼자미 미강 발효물의 항알러지 활성을 확인하기 위하여 비만세포인 RBL-2H3 세포의 hexoamidase 및 histamine 유리 활성을 조사한 결과 슈퍼자미 미강 발효물을 처리하였을 때 각각 약 40% 및 57%의 억제 활성을 나타내어 항알러지 활성을 확인하였다. 3. 슈퍼자미 미강 발효물의 항암 활성을 조사한 결과 복수암 모델 및 고형암 모델에서 모두 암세포의 증식을 억제하는 활성을 나타내었고, 혈액중 백혈구의 수치를 유의적으로 증가하는 것으로 나타나 슈퍼자미 미강 발효물이 항암 활성을 있음을 확인 할 수 있었다. 4. 이상의 결과에서 슈퍼자미 품종의 미강을 버섯 균사체 발효를 통해 얻어진 기능성 소재는 항염, 항알러지, 항암 활성을 통해서 우수한 기능성 소재로서의 개발 가능성이 매우 높다고 판단된다.

루꼴라(Eruca sativa) 추출물의 멜라닌 생성 저해 효과 (Anti-melanogenic effect of Eruca sativa extract)

  • 김현수
    • 한국식품저장유통학회지
    • /
    • 제23권1호
    • /
    • pp.74-79
    • /
    • 2016
  • 본 연구에서 루꼴라(E. sativa)에 대한 다양한 생리활성을 조사하여 기능성소재 응용가능성을 검토하였다. 루꼴라 추출물은 멜라노마 세포에 대하여 낮은 세포독성을 나타냈다. 세포독성이 거의 없는 농도에서 루꼴라 추출물 처리 시 항산화 활성($ID_{50}$, 17.60 mg/L)이 매우 우수하게 나타났으며 루꼴라 추출물 처리시 높은 tyrosinase 활성저해($ID_{50}$, 132.54 mg/L) 및 멜라닌 함량 저하($ID_{50}$, 158.90 mg/L)를 보여주었다. 또한, 루꼴라 추출물 농도 의존적으로 tyrosinase 발현이 억제되었으며, 이는 루꼴라 추출물이 직접적인 tyrosinase 활성저해 및 세포 내 tyrosinase 발현을 억제시킴으로서 멜라닌 합성을 저해하는 것으로 판단된다. 이와 같은 결과로 미루어 볼 때 루꼴라 추출물은 피부미백 소재 등 피부개선 효과를 지닌 기능성 화장품에 활용하기 위한 매우 효과적인 재료가 될 수 있다고 판단되며 향후 주름개선 효과 등 추가적인 실험을 통하여 화장품 소재 개발 응용 가능성을 타진할 것이다.

Passiflora caerulea 추출물의 화장품 소재 활용 가능성 (The Possibility of Passiflora Caerulea Extract as Cosmetic Material)

  • 이재남
    • 한국응용과학기술학회지
    • /
    • 제39권5호
    • /
    • pp.710-719
    • /
    • 2022
  • 본 연구는 Passiflora caerulea 추출물의 항산화 활성 및 멜라닌 생합성 억제 효과 측정을 통해 화장품 소재로서의 활용 가능성을 확인하고자 하였다. Passiflora caerulea 추출물은 70% 에탄올로 추출하였고, TEAC assay를 이용한 ABTS radical 소거능을 측정하였다. 또한 Neutral red assay를 이용한 세포 생존율, DCF-DA를 통한 세포 내 ROS 생성 억제, 멜라닌 생합성 억제 효과를 측정하였다. 연구결과, Passiflora caerulea 추출물의 ABTS radical 소거능은 농도 의존적 소거활성이 확인되었으며, positive control(양성대조군)로 이용한 trolox와 0.1 mg/mL 농도에서는 유사한 radical 소거 활성을 확인하였다. CFDA를 통한 세포 내 활성산소종(ROS) 생성은 농도 의존적으로 억제되었고, B16F10 melanoma 세포에 대한 세포 독성은 나타나지 않았다. 또한 𝛼-MSH로 유도된 멜라닌 생합성 억제 효과를 확인하였다. 따라서 본 연구를 통해 Passiflora caerulea 추출물은 화장품 소재로서의 활용 가능성이 있는 것으로 판단된다.

꾸지뽕나무 추출물의 피부 생리 활성 (Physiological Activities of Cudrania tricuspidata Extracts on the Skin)

  • 최학주;김청택;도민연;랑문정
    • 한국응용과학기술학회지
    • /
    • 제32권2호
    • /
    • pp.260-274
    • /
    • 2015
  • 본 논문은 한국과 중국에서는 전통 한방약재로 오랫동안 사용된 꾸지뽕나무(Cudrania tricuspidata)의 잎, 줄기, 뿌리부분의 에탄올추출물의 물, 에탄올, 에칠아세테이트 용해성 분획물에 대한 피부 생리활성에 관한 실험결과이다. 대식세포인 macrophage(RAW 264.7 cell)에 대하여 이들 분획물들의 nitric oxide 및 염증성 사이토카인 분비 억제효과를 검토한 결과, nitric oxide 생성 억제에는 잎부위의 에칠아세테이트 분획물과 에탄올분획물이, 염증성 사이토카인인 $IL-1{\beta}$ 생성 억제에는 모든 분획물들이 효과가 있고, 염증성 사이토카인인 IL-6 생성 억제에는 잎, 줄기, 뿌리부위의 에칠아세테이트 분획물들이 효과가 있는 것으로 나타났다. 흑색종세포인 melanoma cell(B16-F10 cell)에서 멜라닌 생성억제효과를 측정한 결과, 잎의 에틸아세테이트 분획물 처리에서만 유의성 있는 억제효과를 나타내었다. 주름 개선 효과를 확인하기 위해 인체 정상 피부 섬유아세포( CCD986sk cell)에 대하여 콜라겐의 합성 촉진 효과를 측정한 결과. 잎, 줄기, 뿌리부위의 물 분획물과 잎, 줄기의 에탄올 분획물에서 콜라겐 합성 촉진 효과를 보였다.

쥐 흑색종 세포에서 산화적 스트레스에 의한 MMPs의 발현과 활성에 대한 흑도라지 추출물의 억제 효과 (Inhibitory Effect of Aged Black Platycodi Radix Extract on Expression and Activation of Matrix Metalloproteinases in Oxidative-stressed Melanoma Cells)

  • 채용병;이수진;장호정;박정애;김문무;정경태
    • 생명과학회지
    • /
    • 제20권5호
    • /
    • pp.736-744
    • /
    • 2010
  • 도라지는 민간에서 항궤양, 항진통, 항알러지, 혈관과 히스타민 억제 및 항산화 효과가 있는 것으로 알려져 있고, 그 뿌리인 길경은 아시아에서 식용으로 즐겨먹는 식품 소재로 사포닌이 과량 함유되어 있는 것으로 보고 되어 있으나, 그 작용기전은 과학적으로 해명되지 않았다. 본 연구에서 처음으로 흑도라지가 특정한 공정기술을 이용하여 개발되었으며, 산화적 스트레스 및 MMPs) 대한 ABPRE의 억제 효과를 조사하였다. ABPRE의 항산화효과를 조사하기 위해서 DPPH radical, hydroxyl radical, reducing power, hydrogen peroxide, lipid peroxidation 및 DNA 산화에 대한 연구를 수행하였다. 연구 결과 ABPRE는 DPPH radical 소거에는 효과를 나타내었으나 지질과산화에 의한 malondialdehyde의 생성은 억제하지 않았다. 그러나, ABPRE의 존재 하에서 산화적 DNA 손상이 억제되었다. 또한 gelatin zymography 및 western blot 분석에서 ABPRE는 PMS (phenazine methosulfate)에 의해서 자극된 MMP-2의 발현과 활성을 감소시켰으며, ABPRE는 항산화 효과 및 tyrosinase 발현 억제에 의한 L-DOPA로 유발된 melanin 생성을 저해 하였을 뿐만 아니라 Nrf2에 의해서 조절되는 항산화 효소인 SOD-1과 SOD-2의 발현을 증가시키는 것으로 나타났다. 그러므로 ABPRE는 항산화와 관련 있는 암전이의 예방을 위한 항암제의 후보 소재로 그 가능성이 기대된다.

Melanogenesis regulatory constituents from Premna serratifolia wood collected in Myanmar

  • WOO, SO-YEUN
    • 한국자원식물학회:학술대회논문집
    • /
    • 한국자원식물학회 2019년도 춘계학술대회
    • /
    • pp.21-22
    • /
    • 2019
  • Melanin is a mixture of pigmented biopolymers synthesized by epidermal melanocytes that determine the skin, eye, and hair colors. Melanocytes produce two different kinds of melanin, eumelanin (dark brown/black insoluble pigments found in dark skin and dark hair and pheomelanin (lighter red/yellow). The biological role of melanin is to prevent skin damage by ultraviolet (UV) radiation. However, the overproduction or deficiency of melanin synthesis could lead to serious dermatological problems, which include melasma, melanoderma, lentigo, and vitiligo. Therefore, regulating melanin production is important to prevent the pigmentation disorders. Myanmar has a rich in natural resources. However, the chemical constituents of these natural resources in Myanmar have not been fully investigated. In the effort to search for compounds with anti-melanin deposition activity from Myanmar natural resources, five plants were collected in Myanmar. Extracts of these collected five plants were tested for anti-melanin deposition activity against a mouse melanoma cell line (B16-F10) induced with ${\alpha}$-melanocyte-stimulating hormone (${\alpha}$-MSH) and 3-isobutyl-1-methylxanthine (IBMX), and their anti-melanin deposition activities were compared with the positive control, arbutin. Among the tested extracts, the CHCl3 extracts of the Premna serratifolia (syn: P. integrifolia) wood showed anti-melanin deposition activities with IC50 values of $81.3{\mu}g/mL$. Hence, this study aims to identify secondary metabolites with anti-melanin deposition activity from P. serratifolia wood of Myanmar. P. serratifolia belongs to the Verbenaceae family and is widely distributed in near western sea coast from South Asia to South East Asia, which include India, Malaysia, Vietnam, Cambodia, and Sri Lanka. People in Tanintharyi region located in the southern part of Myanmar utilize the P. serratifolia, Sperethusa crenulata, Naringi crenulata, and Limonia acidissima as Thanaka, traditional cosmetics in Myanmar. Thanaka is applied in the form of paste onto skins to make it smooth and clear, as well as to prevent wrinkles, skin aging, excessive facial oil, pimples, blackheads, and whiteheads. However, the chemical constituents responsible for their cosmetic properties are yet to be identified. Moreover, the chemical constituents of P. serratifolia was almost uncharacterized. Investigation of the P. serratifolia chemical constituents is thus an attractive endeavor to discover new anti-melanin deposition active compounds. The investigation of the chemical constituents of the active CHCl3 extract of P. serratifolia led to isolation of four new lignoids, premnan A (1), premnan B (2), taungtangyiol C (3), and 7,9-dihydroxydolichanthin B (4), together with premnan C (5) (assumed to be an artifact), one natural newlignoid,(3R,4S)-4-(1,3-benzodioxol-5-ylcarbonyl)-3-[(R)-1-(1,3-benzo dioxol-5-yl)-1-hydroxy methyl]tetrahydro-2-furanone (6), and five known compounds (7-11)1,2). The structures of all isolated compounds were determined on the basis of their spectroscopic data and by comparison with the reported literatures. The absolute configurations of 1-3 and 5 were also determined by optical rotation and circular dichroism (CD) data analyses1). The anti-melanin deposition activities of all the isolated compounds were evaluated against B16-F10 cell line. 7,9-Dihydroxydolichanthin B (4) and ($2{\alpha},3{\alpha}$)-olean-12-en-28-oic acid (11) showed strong anti-melanin deposition activities with IC50 values of 18.4 and $11.2{\mu}M$, respectively, without cytotoxicity2). On the other hand, compounds 1-3, 5, and 7 showed melanogenesis enhancing activities1). To better understand their anti-melanin deposition mechanism, the effects of 4 and 11 on tyrosinase activities were investigated. The assay indicated that compounds 4 and 11 did not inhibit tyrosinase. Furthermore, we also examined the mRNA expression of microphthalmia-associated transcription factor (MITF), tyrosinase (TYR), tyrosinase-related protein-1 (TRP-1), and tyrosinase-related protein-2 (TRP-2). Compounds 4 and 11 down-regulated the expression of Tyr and Mitf mRNAs, respectively. Although the P. serratifolia wood has been used as traditional cosmetics in Myanmar for centuries, there are no scientific evidences to support its effectiveness as cosmetics. Investigation of the anti-melanin deposition activity of the chemical constituents of P. serratifolia thus provided insight into the effectiveness of the P. serratifolia wood as a cosmetic agent.

  • PDF

Anti-Angiogenic Activity of Mouse N-/C-terminal deleted Endostatin

  • Cho, Hee-Yeong;Kim, Woo-Jean;Lee, Sae-Won;Kim, Young-Mi;Choi, Eu-Yul;Park, Yong-Suk;Kwon, Young-Guen;Kim, Kyu-Won
    • BMB Reports
    • /
    • 제34권3호
    • /
    • pp.206-211
    • /
    • 2001
  • Endostatin, a proteolytic fragment of collagen XVIII, is a potent inhibitor of angiogenesis and the growth of several primary tumors. However, the opinions on the activity of endostatin derivatives deleted N- or C- terminal are still controversial. In this regard, we produced mouse endostatin and its derivatives in the prokaryotic system, and studied their anti-tumor activity. The [$^3H$]-thymidine incorporation assay demonstrated that N-terminal deleted mouse endostatin, and a C- and N-terminal deleted mutant, effectively inhibited the proliferation of human umbilical vein endothelial cells (HUVECs). The biological activity of endostatin was also shown by its in vivo anti-angiogenic ability on the chorioallantoic membrane (CAM) of a chick embryo. Treatment of $200\;{\mu}g$ of mouse endostatin, or N-terminal deleted mouse endostatin, inhibited capillary formation of CAM 45 to 71%, which is comparative to a 80% effect of positive control, $1\;{\mu}g$ of retinoic acid. An in vivo mouse tumor growth assay showed that N-terminal deleted mouse endostatin, and the N-/C-terminal deleted mutant, significantly repressed the growth of B16F10 melanoma cells in mice as did the full-length mouse endostatin. According to these results, N-and N-/C-terminal deleted mouse endostatins are the potent inhibitors of tumor growth and angiogenesis.

  • PDF