Characterization of a novel tyrosinase inhibitor, (2RS,4R)-2-(2,4-dihydroxyphenyl) thiazolidine-4-carboxylic acid (MHY384)

被引:31
|
作者
Han, Yu Kyeong [2 ]
Park, Yun Jung
Ha, Young Mi
Park, Daeui
Lee, Ji Yeon
Lee, Naree [3 ]
Yoon, Jeong Hyun
Moon, Hyung Ryong [1 ]
Chung, Hae Young
机构
[1] Pusan Natl Univ, Coll Pharm, Med Chem Lab, Mol Inflammat Res Ctr Aging Intervent MRCA, Pusan 609735, South Korea
[2] Dongnam Inst Radiol & Med Sci, Res Ctr, Pusan 619953, South Korea
[3] Univ Illinois, Dept Biochem, Champaign, IL USA
来源
基金
新加坡国家研究基金会;
关键词
Antityrosinase activity; Melanogenesis; Microphthalmia-associated transcription factor; Cyclic adenosine monophosphate; Skin-whitening agent; Docking analysis; HUMAN MELANOCYTES; MELANOMA-CELLS; CYCLIC-AMP; KOJIC ACID; MELANOGENESIS; SKIN; PIGMENTATION; SIGNAL; MICROPHTHALMIA; MECHANISMS;
D O I
10.1016/j.bbagen.2012.01.001
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
Background: We synthesized (2RS,4R)-2-(2,4-dihydroxyphenyl)thiazolidine-4-carboxylic acid (MHY384) as a potential tyrosinase inhibitor and investigated its antityrosinase activity. Methods: The structure of MHY384 was established using H-1 and C-13 NMR spectroscopy and mass spectral analyses. To investigate dual mechanisms of action of MHY384 for the inhibition of melanin synthesis, we confirmed the inhibitory effect of tyrosinase catalytic activity of MHY384. Then, we confirmed the inhibitory effect of MHY384 on transcription of tyrosinase mRNA through alpha-MSH-induced cAMP-PKA-MITF signaling. In addition, we supported the inhibitory mechanism of MHY384 against tyrosinase using a kinetic study and docking programs. Results: To determine how MHY384 regulates melanogenesis, we measured melanin levels and expression of the genes for microphthalmia-associated transcription factor (MITF) and tyrosinase in alpha-melanocyte-stimulating hormone (alpha-MSH)-induced B16F10 melanoma cells. MHY384 potently inhibited tyrosinase activity and melanin production in B16F10 melanoma cells. Through docking models, we were able to construct the tertiary structure of mushroom tyrosinase and simulate its docking with MHY384. The result supports that MHY384 strongly interacts with tyrosinase residues in the active site and it can directly inhibit tyrosinase. To investigate additional mechanisms of action of MHY384, we confirmed that the inhibition of tyrosinase activity was found to be due to the modulation of the expression of tyrosinase and its transcription factor, MITF, through CAMP, which regulates protein kinase A. Conclusions: This study strongly indicates that the depigmenting effect of MHY384 results from the down-regulation of MITF and tyrosinase through direct tyrosinase inhibition. General significance: Our findings suggest that MHY384 can be an effective skin-whitening agent. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:542 / 549
页数:8
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