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辣椒素可逆转甘草查尔酮A/β-熊果苷对B16小鼠黑色素瘤细胞中酪氨酸酶表达的抑制作用。

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

作者信息

Hong Jun-Hui, Chen Huo-Ji, Xiang Shi-Jian, Cao Si-Wei, An Bai-Chao, Ruan Shi-Fa, Zhang Bin, Weng Li-Dong, Zhu Hong-Xia, Liu Qiang

机构信息

Department of Chinese medicine preparation, School of Traditional Chinese Medicine, P R China.

Department of Pharmacy, The affiliated hospital of Qingdao University, 266071, P R China.

出版信息

Pharmacogn Mag. 2018 Jan-Mar;14(53):110-115. doi: 10.4103/pm.pm_103_17. Epub 2018 Feb 20.

Abstract

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. 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 salt; PVDF: Polyvinylidene fluoride; ECL: Enhanced chemiluminescence.

摘要

引言

黑色素由位于皮肤基底层的黑素细胞合成。合成后,黑色素进一步沉积在皮肤表面形成黑斑或黄褐斑。酪氨酸酶是一种在黑色素生成中起重要作用的限速酶。目前,有许多药物可抑制酪氨酸酶表达以进一步减少黑色素生成。然而,其中一些药物在同时使用时可能会逆转其他药物的药理作用。

材料与方法

用酪氨酸酶抑制剂甘草查尔酮A和β - 熊果苷单独或与辣椒中发现的生物碱辣椒素联合处理B16小鼠黑色素瘤细胞。测定细胞毒性、黑色素含量以及酪氨酸酶活性和表达。

结果

当单独应用于B16小鼠黑色素瘤细胞时,甘草查尔酮A/β - 熊果苷抑制酪氨酸酶表达并进一步阻碍黑色素合成。然而,甘草查尔酮A/β - 熊果苷与50μmol/L辣椒素联合使用时会增强这些细胞中酪氨酸酶的表达并进一步增加黑色素含量。

结论

我们的数据表明辣椒素可逆转甘草查尔酮A/β - 熊果苷对B16小鼠黑色素瘤细胞中酪氨酸酶表达的抑制作用。

总结

用酪氨酸酶抑制剂甘草查尔酮A和β - 熊果苷单独或与辣椒中发现的生物碱辣椒素联合处理B16小鼠黑色素瘤细胞。测定细胞毒性、黑色素含量以及酪氨酸酶活性和表达。当单独应用于B16小鼠黑色素瘤细胞时,甘草查尔酮A/β - 熊果苷抑制酪氨酸酶表达并进一步阻碍黑色素合成。然而,甘草查尔酮A/β - 熊果苷与50μmol/L辣椒素联合使用时会增强这些细胞中酪氨酸酶的表达并进一步增加黑色素含量。我们的研究表明辣椒素可逆转甘草查尔酮A/β - 熊果苷对B16小鼠黑色素瘤细胞中酪氨酸酶表达的抑制作用。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;DMSO:二甲基亚砜;RPMI:罗斯威尔帕克纪念研究所;MTT:3 -(4,5 - 二甲基 - 2 - 噻唑基)- 2,5 - 二苯基 - 2 - H - 四氮唑溴盐;NaOH:氢氧化钠;PBS:磷酸盐缓冲盐水;RIPA:放射免疫沉淀测定法;PMSF:苯甲基磺酰氟;SDS:十二烷基硫酸钠;PVDF:聚偏二氟乙烯;ECL:增强化学发光法

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ad7/5858230/465076ad7d49/PM-14-110-g001.jpg

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