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Modulation effects of sweroside isolated from the Lonicera japonica on melanin synthesis

机译:铜苷中分离的调节效果与甘白酶LINONERA japonica对黑色素合成

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In the course of screening for the melanogenesis inhibitors, sweroside was isolated from Lonicera japonica. Its chemical structure was determined on the basis of spectroscopic analysis, including mass spectroscopy and nuclear magnetic resonance analysis. Sweroside inhibited potent melanogenesis in melan-a cells at 300 mu M without cytotoxicity. Also, sweroside decreased tyrosinase, tyrosinase-related protein-1 (TRP-1) and TRP-2 protein production in melan a cells. To identify the signaling pathway of sweroside, the ability of sweroside to influence Akt and extracellular signal-regulated protein kinase (ERK) activation was investigated. Sweroside induced Akt and ERK in a dose-dependent manner. In addition, the specific inhibition of the Akt and ERK signaling pathways were studied by specific inhibitor LY294002 and U0126, respectively and it was causing the increased melanin synthesis. Furthermore, sweroside presented inhibition of the body pigmentation and tyrosinase activity in zebrafish in vivo model. These results suggest that sweroside isolated from L. japonica may be an effective skin-whitening agent through the regulates the expression of MAP kinase and melanogenic enzymes. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:在筛选素瘤抑制剂的过程中,铜醇素被与Lonicera japonica分离。其化学结构是在光谱分析的基础上确定的,包括质谱和核磁共振分析。铜醇素抑制MELAN-CELES在300μm的细胞中抑制有效的糖胺,没有细胞毒性。此外,铜醇素在Melan细胞中降低了酪氨酸酶,酪氨酸酶相关蛋白-1(TRP-2)和TRP-2蛋白质产生。为了鉴定铜醇素的信号通路,研究了铜醇素以影响AKT和细胞外信号调节蛋白激酶(ERK)活化的能力。铜醇素以剂量依赖性方式诱导AKT和ERK。此外,通过特异性抑制剂LY294002和U0126研究了AKT和ERK信号传导途径的特异性抑制,并导致黑色素合成增加。此外,在体内模型中呈斑马鱼中体色素沉着和酪氨酸酶活性的抑制作用。这些结果表明,通过调节MAP激酶和丝酶的表达,粳稻分离的铜醇溶糖苷可以是有效的皮肤美白剂。 (c)2015 Elsevier Ireland Ltd.保留所有权利。

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