- 作者：Yu Kyeong Han<sup>asup><sup> ; sup><sup>bsup><sup> ; sup><sup>csup><sup> ; sup><sup>1sup> ; Yun Jung Park<sup>asup><sup> ; sup><sup>bsup><sup> ; sup><sup>1sup> ; Young Mi Ha<sup>asup><sup> ; sup><sup>bsup><sup> ; sup><sup>1sup> ; Daeui Park<sup>asup><sup> ; sup><sup>bsup> ; Ji Yeon Lee<sup>asup><sup> ; sup><sup>bsup> ; Naree Lee<sup>dsup> ; Jeong Hyun Yoon<sup>bsup> ; Hyung Ryong Moon<sup>asup><sup> ; sup><sup>bsup><sup> ; sup><sup>mhr108@pusan.ac.krsup> ; Hae Young Chung<sup>asup><sup> ; sup><sup>bsup><sup> ; sup><sup>hyjung@pusan.ac.krsup>
- 关键词：ANOVA ; Analysis of variance ; CREB ; cAMP responsive element binding protein ; CO2 ; Carbon dioxide ; CBP ; CREB-binding protein ; cAMP ; Cyclic adenosine monophosphate ; CDCl3 ; Deuterated chloroform ; l-DOPA ; l-3 ; 4-dihydroxyphenylalanine ; DMSO ; Dimethyl sulfoxide
- 刊名：Biochimica et Biophysica Acta (BBA)/General Subjects
- 出版年：2012
- 期刊代码：16_03044165
- 类别：bio
- 出版时间：April, 2012
- 卷：1820
- 期：4
- 页码：542-549
- 文件大小：1429 K
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 <sup>1sup>H and <sup>13sup>C 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 伪-melanocyte-stimulating hormone (伪-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.