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

IF 2.5 Q3 ONCOLOGY
Min Chang Oh, Pincha Devage Sameera Madushan Fernando, Mei Jing Piao, Kyoung Ah Kang, Herath Mudiyanselage Udari Lakmini Herath, Jin Won Hyun
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Abstract

Excessive UVB exposure causes development of both malignant and non-malignant melanoma via the secretion of α-melanocyte-stimulating hormone (α-MSH). We investigated whether baicalein (5,6,7-trihydroxyflavone) could inhibit α-MSH-stimulated melanogenesis. Baicalein prevented UVB- and α-MSH-induced melanin production and attenuated α-MSH-stimulated tyrosinase (monophenol monooxygenase) activity, and expression of tyrosinase and tyrosine-related protein-2. In addition, baicalein prevented melanogenesis and pigmentation via the p38 mitogen-activated protein kinases signaling pathway. These findings suggest that baicalein represents a natural compound for attenuating melanogenesis.

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黄芩素通过p38丝裂原激活蛋白激酶途径抑制B16F10小鼠黑色素瘤细胞中α-刺激黑色素细胞激素刺激的黑色素生成
过量的UVB暴露通过α-促黑素细胞激素(α-MSH)的分泌导致恶性和非恶性黑色素瘤的发展。我们研究了黄芩素(5,6,7-三羟基黄酮)是否能抑制α- msh刺激的黑色素生成。黄芩素可以抑制UVB-和α- msh诱导的黑色素生成,减弱α- msh刺激的酪氨酸酶(单酚单加氧酶)活性,降低酪氨酸酶和酪氨酸相关蛋白-2的表达。此外,黄黄素通过p38丝裂原激活蛋白激酶信号通路阻止黑色素形成和色素沉着。这些发现表明黄芩素是一种天然的抑制黑色素生成的化合物。
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