S-(-)-10,11-Dihydroxyfarnesoic Acid Methyl Ester Inhibits Melanin Synthesis in Murine Melanocyte Cells

被引:10
作者
Baek, Seung-Hwa [1 ]
Ahn, Jun-Won [2 ,3 ]
Nam, Sung-Hee [4 ]
Yoon, Cheol-Sik [5 ]
Shin, Jae-Cheon [6 ]
Lee, Sang-Han [1 ,2 ,7 ]
机构
[1] Kyungpook Natl Univ, Grad Sch, Dept Food Sci & Biotechnol, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Grad Sch, Dept Nanosci & Technol, Taegu 702701, South Korea
[3] Nano Convergence Pract Applicat Ctr, Taegu 704801, South Korea
[4] Rural Adm Agcy, Natl Acad Agr Sci, Dept Agr Biol, Suwon 441707, South Korea
[5] Mycoplus Co Ltd, Anyang 431080, South Korea
[6] Pohang Ctr Evaluat Biomat, Pohang 790834, South Korea
[7] Kyungpook Natl Univ, Food & Bioind Res Inst, Taegu 702701, South Korea
关键词
dihydroxyfarnesoic acid; melanin; tyrosinase; inhibitor; insect juvenile hormone; whitening; SKIN; PIGMENTATION; MELANOGENESIS; PROTECTION; AGENTS;
D O I
10.3390/ijms150712750
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of antimelanogenic agents is important for the prevention of serious aesthetic problems such as melasmas, freckles, age spots, and chloasmas. In the course of screening for melanin synthesis inhibitors, we found that the culture broth from an insect morphopathogenic fungus, Beauveria bassiana CS1029, exhibits potent antimelanogenic activity. We isolated and purified an active metabolite and identified it as S-(-)-10,11-dihydroxyfarnesoic acid methyl ester (dhFAME), an insect juvenile hormone. To address whether dhFAME inhibits melanin synthesis, we first measured the size of the melanin biosynthesis inhibition zone caused by dhFAME. dhFAME also showed inhibitory activity against mushroom tyrosinase in Melan-a cells. Intracellular, dose-dependent tyrosinase inhibition activity was also confirmed by zymography. In addition, we showed that dhFAME strongly inhibits melanin synthesis in Melan-a cells. Furthermore, we compared levels of TYR, TRP-1, TRP-2, MITF, and MC1R mRNA expression by reverse-transcription polymerase chain reaction and showed that treatment of Melan-a cells with 35 mu M dhFAME led to an 11-fold decrease in TYR expression, a 6-fold decrease in TRP-2 expression, and a 5-fold decrease in MITF expression. Together, these results indicate that dhFAME is a potent inhibitor of melanin synthesis that can potentially be used for cosmetic biomaterial(s).
引用
收藏
页码:12750 / 12763
页数:14
相关论文
共 29 条
[1]   Regulation of melanin synthesis by selenium-containing carbohydrates [J].
Ahn, SJ ;
Koketsu, M ;
Ishihara, H ;
Lee, SM ;
Ha, SK ;
Lee, KH ;
Kang, TH ;
Kim, SY .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2006, 54 (03) :281-286
[2]   Quasi-Drugs Developed in Japan for the Prevention or Treatment of Hyperpigmentary Disorders [J].
Ando, Hideya ;
Matsui, Mary S. ;
Ichihashi, Masamitsu .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2010, 11 (06) :2566-2575
[3]  
[Anonymous], 2013, Image J Software 1.48 version., Patent No. 101239631
[4]   Postinflammatory Hyperpigmentation Etiologic and Therapeutic Considerations [J].
Callender, Valerie D. ;
St Surin-Lord, Sharleen ;
Davis, Erica C. ;
Maclin, Marissa .
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2011, 12 (02) :87-99
[5]  
Videira IFD, 2013, AN BRAS DERMATOL, V88, P76, DOI 10.1590/S0365-05962013000100009
[6]   Evidence that stress to the epidermal barrier influenced the development of pigmentation in humans [J].
Elias, Peter M. ;
Menon, Gopinathan ;
Wetzel, Bruce K. ;
Williams, John W. .
PIGMENT CELL & MELANOMA RESEARCH, 2009, 22 (04) :420-434
[7]   Depigmentation Effect of Kadsuralignan F on Melan-A Murine Melanocytes and Human Skin Equivalents [J].
Goh, Myeong-Jin ;
Lee, Hae-Kwang ;
Cheng, Liang ;
Kong, De-Yun ;
Yeon, Jae-Ho ;
He, Quan-Quan ;
Cho, Jun-Cheol ;
Na, Yong Joo .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2013, 14 (01) :1655-1666
[8]   MGRN1-dependent pigment-type switching requires its ubiquitination activity but not its interaction with TSG101 or NEDD4 [J].
Gunn, Teresa M. ;
Silvius, Derek ;
Bagher, Pooneh ;
Sun, Kaihua ;
Walker, Katherine K. .
PIGMENT CELL & MELANOMA RESEARCH, 2013, 26 (02) :263-268
[9]   Wnt3a inhibits proliferation but promotes melanogenesis of melan-a cells [J].
Guo, Haiying ;
Yang, Ke ;
Deng, Fang ;
Xing, Yizhan ;
Li, Yuhong ;
Lian, Xiaohua ;
Yang, Tian .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2012, 30 (03) :636-642
[10]  
Hearing Vincent J, 2011, J Invest Dermatol, V131, pE8, DOI 10.1038/skinbio.2011.4