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本文引用的文献

1
In vitro and in vivo evaluation of ellagic acid on melanogenesis inhibition.体外和体内评估鞣花酸对黑色素生成的抑制作用。
Int J Cosmet Sci. 2000 Aug;22(4):291-303. doi: 10.1046/j.1467-2494.2000.00023.x.
2
Kojic acid -absence of tumor-initiating activity in rat liver, and of carcinogenic and photo-genotoxic potential in mouse skin.曲酸——在大鼠肝脏中无肿瘤启动活性,在小鼠皮肤中无致癌和光遗传毒性潜力。
J Toxicol Sci. 2007 May;32(2):143-59. doi: 10.2131/jts.32.143.
3
Approaches to identify inhibitors of melanin biosynthesis via the quality control of tyrosinase.通过酪氨酸酶的质量控制来鉴定黑色素生物合成抑制剂的方法。
J Invest Dermatol. 2007 Apr;127(4):751-61. doi: 10.1038/sj.jid.5700683. Epub 2007 Jan 11.
4
Hydroquinone and its analogues in dermatology - a potential health risk.对苯二酚及其类似物在皮肤病学中的应用——潜在的健康风险。
J Cosmet Dermatol. 2005 Jun;4(2):55-9. doi: 10.1111/j.1473-2165.2005.40202.x.
5
Hypopigmenting agents: an updated review on biological, chemical and clinical aspects.色素减退剂:关于生物学、化学和临床方面的最新综述
Pigment Cell Res. 2006 Dec;19(6):550-71. doi: 10.1111/j.1600-0749.2006.00334.x.
6
Centaureidin promotes dendrite retraction of melanocytes by activating Rho.矢车菊素通过激活Rho促进黑素细胞的树突回缩。
Biochim Biophys Acta. 2006 Mar;1760(3):487-94. doi: 10.1016/j.bbagen.2006.01.003. Epub 2006 Jan 27.
7
Tyrosinase maturation through the mammalian secretory pathway: bringing color to life.酪氨酸酶通过哺乳动物分泌途径的成熟:赋予生命色彩。
Pigment Cell Res. 2006 Feb;19(1):3-18. doi: 10.1111/j.1600-0749.2005.00288.x.
8
Inhibitory effects of 4-n-butylresorcinol on tyrosinase activity and melanin synthesis.4-正丁基间苯二酚对酪氨酸酶活性和黑色素合成的抑制作用。
Biol Pharm Bull. 2005 Dec;28(12):2216-9. doi: 10.1248/bpb.28.2216.
9
Tyrosinase inhibitors from natural and synthetic sources: structure, inhibition mechanism and perspective for the future.天然和合成来源的酪氨酸酶抑制剂:结构、抑制机制及未来展望
Cell Mol Life Sci. 2005 Aug;62(15):1707-23. doi: 10.1007/s00018-005-5054-y.
10
Lactic acid as a new therapeutic peeling agent in melasma.乳酸作为黄褐斑治疗的新型剥脱剂。
Dermatol Surg. 2005 Feb;31(2):149-54; discussion 154. doi: 10.1111/j.1524-4725.2005.31035.

在日本研发的用于预防或治疗色素沉着紊乱的准药品。

Quasi-drugs developed in Japan for the prevention or treatment of hyperpigmentary disorders.

作者信息

Ando Hideya, Matsui Mary S, Ichihashi Masamitsu

机构信息

Skin Aging and Photo-aging Research Center, Doshisha University, Kizugawa, Kyoto 619-0225, Japan; E-Mail:

出版信息

Int J Mol Sci. 2010 Jun 18;11(6):2566-75. doi: 10.3390/ijms11062566.

DOI:10.3390/ijms11062566
PMID:20640168
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2904932/
Abstract

Excess production of melanin or its abnormal distribution, or both, can cause irregular hyperpigmentation of the skin, leading to melasma and age spots. To date, various quasi-drugs that prevent or improve hyperpigmentary disorders have been developed and officially approved by the Ministry of Health, Labor and Welfare of Japan. Many of these inhibit the activity of tyrosinase, an enzyme required for melanin synthesis, for example, by competitive or non-competitive inhibition of its catalytic activity, by inhibiting its maturation, or by accelerating its degradation. In this review, we categorize the quasi-drugs developed in Japan to prevent or treat hyperpigmentary disorders, or both, and discuss perspectives for future development.

摘要

黑色素生成过多或其分布异常,或两者兼而有之,可导致皮肤出现不规则色素沉着,引发黄褐斑和老年斑。迄今为止,日本厚生劳动省已研发并正式批准了多种预防或改善色素沉着紊乱的准药品。其中许多药物通过竞争性或非竞争性抑制其催化活性、抑制其成熟或加速其降解等方式,抑制酪氨酸酶(黑色素合成所需的一种酶)的活性。在本综述中,我们对日本研发的用于预防或治疗色素沉着紊乱或两者兼治的准药品进行了分类,并探讨了未来的发展前景。