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来自民间药物榕属植物的去甲氧基醉椒素在 B16F10 细胞和小鼠皮肤中表现出无细胞毒性的黑色素生成抑制剂作用。

Norartocarpetin from a folk medicine Artocarpus communis plays a melanogenesis inhibitor without cytotoxicity in B16F10 cell and skin irritation in mice.

机构信息

Department of Fragrance and Cosmetic Science, College of Pharmacy, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

BMC Complement Altern Med. 2013 Dec 10;13:348. doi: 10.1186/1472-6882-13-348.

Abstract

BACKGROUND

Many natural products used in preventive medicine have also been developed as cosmeceutical ingredients in skin care products, such as Scutellaria baicalensis and Gardenia jasminoides. Norartocarpetin is one of the antioxidant and antityrosinase activity compound in Artocarpus communis; however, the cytotoxicity, skin irritation and antimelanogenesis mechanisms of norartocarpetin have not been investigated yet.

METHODS

In the present study, cell viability in vitro and skin irritation in vivo are used to determine the safety of norartocarpetin. The melanogenesis inhibition of norartocarpetin was determined by cellular melanin content and tyrosinase in B16F10 melanoma cell. Moreover, we examined the related-melanogenesis protein by western blot analysis for elucidating the antimelanogenesis mechanism of norartocarpin.

RESULTS

The result of the present study demonstrated that norartocarpetin not only present non-cytotoxic in B16F10 and human fibroblast cells but also non-skin irritation in mice. Moreover, our result also first found that norartocarpetin downregulated phospho-cAMP response element-binding (phospho-CREB) and microphthalmia-associated transcription factor (MITF) expression, which in turn decreased both synthesis of tyrosinases (TRP-1 and TRP-2) and cellular melanin content. This process is dependent on norartocarpetin phosphorylation by mitogen-activated protein kinases such as phospho-JNK and phospho-p38, and it results in decreased melanogenesis.

CONCLUSION

The present study suggests that norartocarpetin could be used as a whitening agent in medicine and/or cosmetic industry and need further clinical study.

摘要

背景

许多用于预防医学的天然产物也被开发为护肤品中的化妆品成分,如黄芩和栀子。山栀子中的紫檀芪是一种具有抗氧化和酪氨酸酶活性的化合物;然而,紫檀芪的细胞毒性、皮肤刺激性和抗黑色素生成机制尚未得到研究。

方法

在本研究中,体外细胞活力和体内皮肤刺激用于确定紫檀芪的安全性。通过 B16F10 黑色素瘤细胞中的细胞黑色素含量和酪氨酸酶来确定紫檀芪的黑色素生成抑制作用。此外,我们通过 Western blot 分析检查了相关的黑色素生成蛋白,以阐明紫檀芪的抗黑色素生成机制。

结果

本研究结果表明,紫檀芪不仅在 B16F10 和人成纤维细胞中无细胞毒性,而且在小鼠中也无皮肤刺激性。此外,我们的结果还首次发现紫檀芪下调磷酸化 cAMP 反应元件结合蛋白(磷酸化 CREB)和小眼畸形相关转录因子(MITF)的表达,进而降低了酪氨酸酶(TRP-1 和 TRP-2)的合成和细胞黑色素含量。这个过程依赖于丝裂原活化蛋白激酶(如磷酸化 JNK 和磷酸化 p38)对紫檀芪的磷酸化,从而导致黑色素生成减少。

结论

本研究表明,紫檀芪可作为医学和/或化妆品工业中的美白剂,并需要进一步的临床研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25dc/3878891/7148194872c7/1472-6882-13-348-1.jpg

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