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Capsaicin reverses the inhibitory effect of licochalcone A/β-Arbutin on tyrosinase expression in b16 mouse melanoma cells

机译:辣椒素逆转了甘草甜菜碱A /β-熊果苷对b16小鼠黑素瘤细胞酪氨酸酶表达的抑制作用

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Introduction: Melanin is synthesized by melanocytes, which are located in the basal layer of the skin. After synthesis, melanin is further deposited on the surface of the skin to form black spots or chloasma. Tyrosinase is a rate-limiting enzyme that plays an important role in melanogenesis. Currently, there are many drugs that inhibit tyrosinase expression to further reduce melanogenesis. Nevertheless, some of these could reverse the pharmacological effect of other drugs, when used simultaneously. Materials and Methods: B16 mouse melanoma cells were treated with the tyrosinase inhibitors licochalcone A and β-arbutin, alone or in combination with capsaicin, an alkaloid found in peppers. Cytotoxicity, melanin content, and tyrosinase activity and expression were determined. Results: Licochalcone A/β-arbutin inhibited tyrosinase expression and further hindered melanin synthesis when applied individually to B16 mouse melanoma cells. However, licochalcone A/β-arbutin combined with 50 μmol/L capsaicin enhanced the expression of tyrosinase in these cells and further increased melanin content. Conclusion: Our data implied that capsaicin could reverse the inhibitory effect of licochalcone A/β-arbutin on tyrosinase expression in B16 mouse melanoma cells. SUMMARY B16 mouse melanoma cells were treated with the tyrosinase inhibitors licochalcone A and β-arbutin, alone or in combination with capsaicin, an alkaloid found in peppers. Cytotoxicity, melanin content, and tyrosinase activity and expression were determined. Licochalcone A/β-arbutin inhibited tyrosinase expression and further hindered melanin synthesis when applied individually to B16 mouse melanoma cells. However, licochalcone A/β-arbutin combined with 50 μmol/L capsaicin enhanced the expression of tyrosinase in these cells and further increased melanin content. Our research implied that capsaicin could reverse the inhibitory effect of licochalcone A/β-arbutin on tyrosinase expression in B16 mouse melanoma cells. Abbreviations used: B16: B16 mouse melanoma cells; L-DOPA: 3, 4-L-dihydroxyphenylalanine; TYR: Tyrosinase; USP: United States Pharmacopeia; FBS: Fetal bovine serum; EDTA: Ethylenediaminetetraacetic acid; DMSO: Dimethyl sulfoxide; RPMI: Roswell Park Memorial Institute; MTT3: 4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide, NaOH: Sodium hydroxide; PBS: Phosphate-buffered saline; RIPA: Radio-immunoprecipitation assay; PMSF: Phenylmethanesulfonyl fluoride or phenylmethylsulfonyl fluoride; SDS: Sodium dodecyl sulfate, sodium sa PVDF: Polyvinylidene fluoride; ECL: Enhanced chemiluminescence. Open in a separate window.
机译:简介:黑色素是由位于皮肤基底层的黑色素细胞合成的。合成后,黑色素进一步沉积在皮肤表面上,形成黑斑或黄褐斑。酪氨酸酶是一种限速酶,在黑色素生成中起重要作用。当前,有许多抑制酪氨酸酶表达以进一步减少黑色素生成的药物。然而,当同时使用时,其中一些可能会逆转其他药物的药理作用。材料和方法:B16小鼠黑素瘤细胞分别用酪氨酸酶抑制剂licochalcone A和β-熊果苷或与辣椒中的生物碱辣椒素结合使用。测定细胞毒性,黑色素含量以及酪氨酸酶活性和表达。结果:单独应用到B16小鼠黑色素瘤细胞中时,Licochalcone A /β-熊果苷可抑制酪氨酸酶的表达,并进一步抑制黑色素的合成。然而,甘草甜菜碱A /β-熊果苷与50μmol/ L辣椒素的结合增强了酪氨酸酶在这些细胞中的表达,并进一步增加了黑色素的含量。结论:我们的数据表明辣椒素可以逆转甘草糖苷A /β-熊果苷对B16小鼠黑素瘤细胞酪氨酸酶表达的抑制作用。总结B16小鼠黑素瘤细胞用酪氨酸酶抑制剂licochalcone A和β-熊果苷单独或与辣椒素(一种辣椒中的生物碱)组合使用。测定细胞毒性,黑色素含量以及酪氨酸酶活性和表达。当分别应用于B16小鼠黑色素瘤细胞时,Licochalcone A /β-熊果苷抑制酪氨酸酶表达并进一步阻碍黑色素的合成。然而,甘草甜菜碱A /β-熊果苷与50μmol/ L辣椒素的结合增强了酪氨酸酶在这些细胞中的表达,并进一步增加了黑色素的含量。我们的研究表明,辣椒素可以逆转甘草糖苷A /β-熊果苷对B16小鼠黑素瘤细胞酪氨酸酶表达的抑制作用。使用的缩写:B16:B16小鼠黑色素瘤细胞; L-DOPA:3,4-L-二羟基苯丙氨酸; TYR:酪氨酸酶; USP:美国药典; FBS:胎牛血清; EDTA:乙二胺四乙酸;乙二胺四乙酸。 DMSO:二甲基亚砜; RPMI:罗斯威尔公园纪念学院; MTT 3:4,5-二甲基-2-噻唑基)-2,5-二苯基-2-H-溴化四唑,NaOH:氢氧化钠; NH 4。 PBS:磷酸盐缓冲盐水; RIPA:放射免疫沉淀试验; PMSF:苯甲磺酰氟或苯甲基磺酰氟; SDS:十二烷基硫酸钠,钠盐; PVDF:聚偏二氟乙烯; ECL:增强化学发光。在单独的窗口中打开。

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