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羟乙基白杨素通过抑制酪氨酸酶活性产生的抗黑色素生成作用及相关方法。

Anti-melanogenic effects of hydroxyethyl chrysin through the inhibition of tyrosinase activity: and approaches.

作者信息

Lee Yuna, Song Ha-Yeon, Byun Eui-Baek

机构信息

Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, Jeongeup, 56212, Republic of Korea.

出版信息

Heliyon. 2025 Jan 4;11(2):e41718. doi: 10.1016/j.heliyon.2025.e41718. eCollection 2025 Jan 30.

DOI:10.1016/j.heliyon.2025.e41718
PMID:39882455
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11774776/
Abstract

The suppression of tyrosinase (TYR), a key enzyme in melanogenesis, has been suggested as an effective strategy for preventing melanin accumulation. We previously discovered the novel chrysin derivative hydroxyethyl chrysin (HE-chrysin) through an irradiation technique, which exerted higher anti-inflammatory and anti-cancer activities than original chrysin. In the present study, we explored whether HE-chrysin has antioxidant and anti-melanogenic capacity using B16F10 murine melanoma cells and molecular docking. HE-chrysin exhibited enhanced antioxidant capacity in DPPH, ABTS, and FRAP assays, and it decreased cellular HO-stimulated reactive oxygen species levels in comparison to original chrysin. At 2.5 μM, HE-chrysin reduced 3-isobutyl-1-methylxanthine-stimulated melanin production significantly by suppressing intracellular TYR activity without cytotoxicity. Furthermore, molecular docking showed that HE-chrysin inhibited TYR activity by interacting with key residues (Glu and Asn) and chelating Cu ions at the active site, with a binding free energy of -7.00 kcal/mol compared with arbutin (-5.12 kcal/mol). Our findings show that HE-chrysin is an anti-melanogenic candidate and a potential antioxidant for use in dermatologic therapy.

摘要

抑制酪氨酸酶(TYR),一种黑色素生成中的关键酶,已被认为是预防黑色素积累的有效策略。我们之前通过辐照技术发现了新型白杨素衍生物羟乙基白杨素(HE-白杨素),其抗炎和抗癌活性高于原始白杨素。在本研究中,我们使用B16F10小鼠黑色素瘤细胞和分子对接技术探究了HE-白杨素是否具有抗氧化和抗黑色素生成能力。在DPPH、ABTS和FRAP测定中,HE-白杨素表现出增强的抗氧化能力,与原始白杨素相比,它降低了细胞内HO刺激的活性氧水平。在2.5 μM时,HE-白杨素通过抑制细胞内TYR活性显著降低了3-异丁基-1-甲基黄嘌呤刺激的黑色素生成,且无细胞毒性。此外,分子对接显示,HE-白杨素通过与关键残基(Glu和Asn)相互作用并在活性位点螯合铜离子来抑制TYR活性,与熊果苷(-5.12 kcal/mol)相比,其结合自由能为-7.00 kcal/mol。我们的研究结果表明,HE-白杨素是一种抗黑色素生成候选物,也是用于皮肤科治疗的潜在抗氧化剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/dd7ec84c8c2a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/0fbc2295e7cc/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/c38f93a5cecb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/b5fffc4a4da5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/e04364279857/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/a2b261612e98/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/dd7ec84c8c2a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/0fbc2295e7cc/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/c38f93a5cecb/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/b5fffc4a4da5/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/e04364279857/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/a2b261612e98/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a02/11774776/dd7ec84c8c2a/gr5.jpg

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Baicalein Inhibits α-Melanocyte-stimulating Hormone-stimulated Melanogenesis via p38 Mitogen-activated Protein Kinase Pathway in B16F10 Mouse Melanoma Cells.
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