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茶黄素 A 的抗黑色素生成作用。

Antimelanogenesis Effects of Theasinensin A.

机构信息

Department of Biocosmetics, Sungkyunkwan University, Suwon 16419, Korea.

Department of Integrative Biotechnology and Biomedical Institute for Convergence at SKKU (BICS), Sungkyunkwan University, Suwon 16419, Korea.

出版信息

Int J Mol Sci. 2021 Jul 12;22(14):7453. doi: 10.3390/ijms22147453.

Abstract

Theasinensin A (TSA) is a major group of catechin dimers mainly found in oolong tea and black tea. This compound is also manufactured with epigallocatechin gallate (EGCG) as a substrate and is refined after the enzyme reaction. In previous studies, TSA has been reported to be effective against inflammation. However, the effect of these substances on skin melanin formation remains unknown. In this study, we unraveled the role of TSA in melanogenesis using mouse melanoma B16F10 cells and normal human epidermal melanocytes (NHEMs) through reverse transcription polymerase chain reaction (RT-PCR), Western blotting analysis, luciferase reporter assay, and enzyme-linked immunosorbent assay analysis. TSA inhibited melanin formation and secretion in α-melanocyte stimulating hormone (α-MSH)-induced B16F10 cells and NHEMs. TSA down-regulated the mRNA expression of (), (), and , which are all related to melanin formation in these cells. TSA was able to suppress the activities of certain proteins in the melanocortin 1 receptor (MC1R) signaling pathway associated with melanin synthesis in B16F10 cells: cyclic adenosine monophosphate (cAMP) response element-binding protein (CREB), protein kinase A (PKA), tyrosinase, and microphthalmia-associated transcription factor (MITF). We also confirmed α-MSH-mediated CREB activities through a luciferase reporter assay, and that the quantities of cAMP were reduced by TSA in the enzyme linked immunosorbent assay (ELISA) results. Based on these findings, TSA should be considered an effective inhibitor of hyperpigmentation.

摘要

茶黄素 A(TSA)是主要存在于乌龙茶和红茶中的儿茶素二聚体。这种化合物也是用表没食子儿茶素没食子酸酯(EGCG)作为底物制造的,并在酶反应后进行精制。在以前的研究中,TSA 已被报道对炎症有效。然而,这些物质对皮肤黑色素形成的影响尚不清楚。在这项研究中,我们使用小鼠黑色素瘤 B16F10 细胞和正常人表皮黑素细胞(NHEM)通过逆转录聚合酶链反应(RT-PCR)、Western blot 分析、荧光素酶报告基因分析和酶联免疫吸附分析来揭示 TSA 在黑色素生成中的作用。TSA 抑制 α-促黑素细胞激素(α-MSH)诱导的 B16F10 细胞和 NHEM 中的黑色素形成和分泌。TSA 下调了这些细胞中与黑色素形成有关的()、()和()的 mRNA 表达。TSA 能够抑制与 B16F10 细胞中黑色素合成相关的黑素皮质素 1 受体(MC1R)信号通路中某些蛋白的活性:环磷酸腺苷(cAMP)反应元件结合蛋白(CREB)、蛋白激酶 A(PKA)、酪氨酸酶和小眼畸形相关转录因子(MITF)。我们还通过荧光素酶报告基因分析证实了 α-MSH 介导的 CREB 活性,并且 TSA 在酶联免疫吸附分析(ELISA)结果中减少了 cAMP 的量。基于这些发现,TSA 应被视为一种有效的过度色素沉着抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ae2/8305159/2cff8662dfb2/ijms-22-07453-g001.jpg

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