• 제목/요약/키워드: Melanin synthesis inhibition

검색결과 187건 처리시간 0.025초

만형자 용매 분획물의 미백 개선 효과 (Whitening Effects of Solvent Fractions Isolated from Vitex rotundifolia)

  • 유재묘;김동희;손준호
    • Journal of Applied Biological Chemistry
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    • 제58권3호
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    • pp.266-271
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    • 2015
  • 최근에는 hyper-pigmentation에 대한 제품 개발을 위해 melanogenesis의 경로에 대한 이해를 위해 많은 노력을 하고 있다. 이에 따라 본 연구에서는 만형자(Vitex rotundifolia)의 depigmentation에 대한 효과를 조사하였다. B16F10 mouse melanoma cell을 이용하여 tyrosinase, MITF, TRP-1, TRP-2 그리고 melanin synthesis의 저해를 확인하였고, 만형자 ethyl acetate 분획물(VR-EA)을 처리하였을 때 농도의존적으로 감소한다는 것을 알 수 있었다. 특히, VR-EA는 tyrosinase와 TRP-1의 경우 각각 53.2, 88.4%의 저해율을 보여 미백에 있어서 효과적인 활성을 보여주었다. 따라서 만형자는 melanin synthesis를 효과적으로 막아주어 미백소재로서 활용 가능성이 충분하다고 사료된다.

대잎 추출물의 멜라닌 합성과 타이로신 활성 저해 효과 (Inhibitory Effects of Phyllostachys bambusoides on Melanin Synthesis and Tyrosinase Activity in Cultured Human Melanoma Cells)

  • 허만규;한민호;박철;최영현
    • 생명과학회지
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    • 제24권3호
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    • pp.284-289
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    • 2014
  • 타이로신은 멜라닌 합성을 조절하는 효소이다. 본 연구에서는 현재까지 미백 효능에 대하여 연구가 진행되지 않은 대나무 중 왕대의 잎 및 대 속 내피 추출물이 유발하는 타이로시나제 활성 및 멜라닌 생성 억제 정도를 조사하였다. 대 잎과 대 속 추출물을 5 mg/ml 농도로 멜라닌 세포에 처리하면 세포의 생존율이 감소하는 것으로 나타났다. 또한 세포독성이 없는 조건의 대 잎과 대 속 추출물을 처리하였을 경우 타이로시나제 활성이 억제되었으며, 멜라닌 생성도 억제되는 것으로 나타났다. 본 연구의 결과를 살펴볼 때 대나무 추출물이 타이로시나제 활성과 발현을 저해함으로써 멜라닌 생성을 억제할 수 있는 후보군으로 가능성이 있는 것으로 생각된다.

B16 흑색종세포에서 로바스타틴에 의한 멜라닌 합성 촉진효과에 미치는 세포내 칼슘의 역할 (Role of Intracellular $Ca^{2+}$ in the Lovastatin-Induced Stimulation of Melanin Synthesis in B16 Melanoma Cells)

  • 이용수
    • 약학회지
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    • 제57권1호
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    • pp.24-31
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    • 2013
  • Although statins, inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, have been shown to increase melanin synthesis, the exact mechanism of this action is not fully understood. In this study we investigated the possible involvement of intracellular $Ca^{2+}$ signal in the mechanism of stimulation of melanin synthesis induced by lovastatin in B16 cells. Lovastatin stimulated the production of melanin in a dose-dependent manner in the cells. Treatment with mevalonate, FPP and GGPP, precursors of cholesterol, did not significantly suppress the lovastatin-induced melanin production, suggesting that inhibition of cholesterol synthesis may not be involved in the mechanism of the action of lovastatin. In addition, lovastatin did not significantly alter the cAMP concentration and the stimulated production of melanin by lovastatin was not significantly changed by treatment with H89, a potent inhibitor of protein kinase A, which demonstrates that cAMP pathway may not be involved. However, lovastatin increased intracellular $Ca^{2+}$ concentration in a dose-related fashion. Treatment with EGTA, an extracellular $Ca^{2+}$ chelator did not significantly alter the lovastatin-induced intracellular $Ca^{2+}$ increase and melanin synthesis, whereas intracellular $Ca^{2+}$ reduction with BAPTA/AM and intracellular $Ca^{2+}$ release blockers (dantrolene and TMB-8) completely blunted these actions of lovastatin. Taken together, these results suggest that the intracellular $Ca^{2+}$ release may play an important role in the lovastatin-induced stimulation of melanin synthesis in B16 cells. These results further suggest that lovastatin may be useful for the treatment of hypopigmentation disorders, such as vitiligo.

백강잠의 멜라닌 생성 억제와 미백효과에 관한 연구 (A Study on the Melanin Synthesis Inhibition and Whitening Effect of Bombysis Corpus)

  • 오한철;임규상;황충연;윤인환;김남권
    • 한방안이비인후피부과학회지
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    • 제20권3호
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    • pp.1-13
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    • 2007
  • Objective : This study was performed to assess the whitening effect of Bombysis Corpus on melanin synthesis. Methods : The whitening effects of Bombysis Corpus were examined by in vitro melanin production assay. We assessed inhibitory effects of Bombysis Corpus on melanin-release from B16F10, on melanin production in B16F10, on mushroom tyrosinase activity in vitro, on tyrosinase activity in B16F10, effect of Bombysis Corpus on the expression tyrosinase, TRP-1, PKA, ERK-1 ERK-2, AKT-1, MITF in B16F10. Results : 1. Bombysis Corpus inhibited melanin-release, melanin production in B16F10. 2. Bombysis Corpus inhibited tyrosinase activity in vitro and in B16F10. 3. Bombysis Corpus suppressed the expression of tyrosinase, TRP-1 in B16F10. 4. Bombysis Corpus suppressed the expression of PKA in B16F10. 5. Bombysis Corpus suppressed the expression of ERK-1, ERK-2, AKT-1 in B16F10. 6. Bombysis Corpus suppressed the expression of MITF in B16F10. Conclusion : The study shows that Bombysis Corpus inhibited melanin production on the melanogenesis.

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Enhancement of Melanin Synthesis by the Branch Extracts of Vaccinium oldhamii through Activating Tyrosinase Activity in B16F10 Melanoma Cells

  • Son, Kun Ho;Baek, Jueng Kyu;Park, Su Bin;Kim, Ha Na;Park, Gwang Hun;Son, Ho-Jun;Eo, Hyun Ji;Song, Jeong Ho;Jeong, Hyung Jin;Jeong, Jin Boo
    • 한국자원식물학회지
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    • 제31권5호
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    • pp.547-553
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    • 2018
  • This study was conducted to investigate the effect of branch extracts of Vaccinium oldhamii (VOB) on melanin synthesis in B16F10 cells. VOB promoted melanin production in absence or presence of ${\alpha}$-melanocyte-stimulating hormone (${\alpha}-MSH$) in B16F10 cells. However, VOB did not affect the expression of tyrosinase and TRP-1 associated with melanin synthesis at the mRNA and protein levels in B16F10. But, VOB decreased TRP-2 protein level and induced tyrosinase activation in B16F10 cells. Inhibition of tyrosinase activity and tyrosinase knockdown attenuated VOB-mediated melanin synthesis. In conclusion, VOB may stimulate melanin synthesis through activating tyrosinase activity.

녹차씨 껍질 에탄올 추출물의 미백 활성 (Whitening Effect of Green Tea Seed Shell Ethanol Extracts)

  • 송하연;성낙윤;정필문;강민수;박원종;변의홍
    • 한국식품영양과학회지
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    • 제44권10호
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    • pp.1470-1475
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    • 2015
  • 본 연구는 산업 부산물의 이용성 향상을 위하여 폐자원인 녹차씨 껍질 추출물의 미백 활성을 평가하기 위하여 수행되었다. 녹차씨 껍질로부터 유용성 성분을 얻기 위하여 에탄올 추출을 한 결과 건조중량 대비 1.24%의 추출물의 수율을 얻을 수 있었고, DPPH 라디칼 소거능 및 tyrosinase 억제능을 관찰한 결과 녹차씨 껍질 추출물의 농도가 증가할수록 활성이 유의적으로 증가하는 것으로 나타났다. 또한 이러한 미백 효과가 세포 내에서도 일어나는지에 관하여 알아보기 위하여 melanoma 세포인 B16BL6에 ${\alpha}$-MSH를 처리하여 melanin의 형성을 촉진시키는 melanogenesis 과정을 유도한 후 녹차씨 껍질 추출물을 처리한 결과 농도 의존적으로 melanin의 형성이 감소되는 것을 알 수 있었다. 이상의 결과로 녹차씨 껍질 추출물의 미백 활성을 확인할 수 있었으며, 이를 활용하여 식품 및 화장품의 기능성 소재로 이용한다면 산업 부산물인 녹차씨 껍질을 활용하는 차원에서 그 경제적 가치가 매우 클 것으로 사료된다.

Efficient Target-Site Assay of Chemicals for Melanin Biosynthesis Inhibition of Magnaporthe grisea

  • Kim, Jin-Cheol;Son, Mi-Jung;Kim, Heung-Tae;Park, Gyung-Ja;Hahn, Hoh-Gyu;Nam, Kee-Dal;Cho, Kwang-Yun
    • The Plant Pathology Journal
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    • 제16권3호
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    • pp.125-129
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    • 2000
  • A rapid and efficient assay to determine melanin biosynthesis inhibition of Magnaporthe grisea, a causal agent of the rice blast, by chemicals was developed. Wells in 24-well plates were loaded with spore suspension of the fungus and three known melanin biosynthesis inhibitors of KC10017, tricyclazole, and carpropamid. Subsequent color changes of mycelia and culture media in the wells were observed 7 days after incubation. The wells treated with KC10017 (an inhibitor of polyketide synthesis step and/or pentaketide cyclization step) became colorless, whereas tricyclazole (an inhibitor of 1, 3, 8-trihydroxynaphthalene reductase) or carpropamid (an inhibitor of scytalone dehydratase)-treated wells exhibited red color. They did not show any inhibitory effect on fungal growth. The inhibition of reaction steps prior to 1, 3, 6, 8-tetrahydroxynaphthalene formation was easily determined by colorless medium and mycelia. However, it was impossible to distinguish between inhibition of reduction steps and inhibition of dehydration steps by colors of the cultures. It was accomplished through HPLC analysis of the melanin biosynthesis-involving pentaketide metabolites accumulated by the inhibitors. Through screening of a number of synthetic chemicals using the in vitro assay, we could find a novel chemical group of melanin biosynthesis inhibitor.

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Inhibitory Effects of Plant Extracts on Tyrosinase Activity and Melanin Synthesis

  • Park, Hyen-Joo;Park, Kwang-Kyun;Hwang, Jae-Kwan;Chung, Won-Yoon;Lee, Seung-Eun;Lee, Sang-Kook
    • Natural Product Sciences
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    • 제16권2호
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    • pp.133-139
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    • 2010
  • In order to develop a new skin whitening agent, approximately 100 plant extracts were evaluated for their inhibitory activities against melanin biosynthesis in cultured mouse melanocyte melan-a cells. As a result, seven extracts exhibited over 50% inhibition of melanin synthesis compared to control at a concentration of $20\;{\mu}g/ml$. In particular, Aster ageratoides Turcz. var. ageratoides (branch, root, aerial, flower; $IC_{50}$ = 17.3, 6.1, 13.6, $12.9\;{\mu}g/ml$, respectively) and Physalis alkekengi var. francheti (leaf, unripen fructus, aerial; $IC_{50}$ = 6.5, 28.3, $23.9\;{\mu}g/ml$) markedly inhibited melanin synthesis. In addition, tyrosinase activity was monitored by the measurement of dopachrome formation from the oxidation of L-3,4-dihydroxyphenylalanine. Extracts of A. ageratoides Turcz. var. ageratoides (flower) and P. alkekengi var. francheti (leaf) showed the most potent tyrosinase inhibitory activity. These plants might be the potential candidate sources in the development of novel skin-whitening products.

노무라입깃해파리 가수분해 추출물의 멜라닌합성 저해효과 (Melanogenesis Inhibition Effects of Nemopilema nomurai Hydrolized Extracts)

  • 이하연;김영훈;엄선영;정욱순;장문식;이남호
    • 대한화장품학회지
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    • 제40권4호
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    • pp.341-347
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    • 2014
  • 본 연구에서는 노무라입깃해파리(Nemopilema nomurai) 가수분해 추출물의 미백활성에 대하여 검색하였다. 가수분해 시료(NHE, N. nomurai Hydrolized Extract)는 노무라입깃해파리를 상업용 단백질분해효소(Protamex, Alcalase, Flavourzyme, Neutrase)를 이용하여 $55^{\circ}C$에서 pH 5-8 조건으로 처리하는 과정을 거쳐 얻었다. 미백활성은 B16-F1 멜라노마 세포에서 멜라닌 색소 합성 저해능 평가를 통하여 확인하였다. 실험결과, Neutrase로 처리된 시료(N-NHE)에서 $100{\mu}g/mL$의 농도에서 멜라닌 생성이 가장 효율적으로 89.9% 감소되는 것을 관찰하였다. 이 시료는 또한 tyrosinase와 TRP-1 (tyrosinase related protein-1) 단백질의 발현을 억제하였다. 이상의 연구 결과는 노무라입깃해파리 가수분해 추출물의 화장품 미백 소재로의 개발 가능성을 보여주고 있다.

Melanin synthesis and skin wrinkle inhibitory effects of the medicinal mushroom Ganoderma applanatum

  • Yoon, Ki Nam;Lee, Tae Soo
    • 한국버섯학회지
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    • 제19권3호
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    • pp.150-159
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    • 2021
  • Anti-melanogenesis and skin anti-wrinkle effects of methanol (ME) and hot water (HE) extracts from the fruiting bodies of Ganoderma applanatum were investigated in this study. The total phenolic contents of the ME and HE of the mushroom were 11.68 and 3.15 ㎍ GAEs/mg, respectively, whereas the total flavonoid contents of the ME and HE were 21.82 and 2.69 ㎍ QEs/mg, respectively. The survival rate of B16-F10 murine melanoma cells treated with 750 ㎍ ME and HE were 83.46% and 85.54%, respectively, thereby suggesting that mushroom extracts were slightly cytotoxic at the tested concentration. The in vitro tyrosinase inhibition by ME (83.15%) and HE (83.44%) was significantly lower than that of kojic acid (99.61%), the positive control, at 2.0 mg/mL. Although the inhibition of cellular melanin synthesis in B16-F10 melanoma cells by 2.0 mg/mL of ME (50.24%) and HE (51.24%) was lower than that of arbutin (64.84%), the inhibition by both ME and HE was higher than 50%. Collagenase inhibition by HE was comparable to 2.0 mg/mL epigallocatechin (EGCG), the positive control; however, elastase inhibition by ME and HE was lower than that of EGCG at the concentration tested. The results showed that the fruiting bodies of G. applanatum had good anti-tyrosinase, good anti-collagenase, and moderate anti-elastase activities, which might be useful for developing novel skin-whitening and anti-wrinkle agents.