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黄花蒿乙醇提取物具有抗光老化活性。

Artemisia asiatica ethanol extract exhibits anti-photoaging activity.

机构信息

Department of Genetic Engineering and Biomedical Institute for convergence (BICS), Sungkyunkwan University, Suwon 16419, Republic of Korea.

Research and Business Foundation, Sungkyunkwan University, Suwon 16419, Republic of Korea.

出版信息

J Ethnopharmacol. 2018 Jun 28;220:57-66. doi: 10.1016/j.jep.2018.03.037. Epub 2018 Mar 31.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Artemisia asiatica Nakai is a traditional herbal plant that has long been used in anti-inflammatory, anti-infective and skin protective remedies.

AIM OF THE STUDY

In this study, traditionally known skin-protective activity of Artemisia asiatica Nakai was examined with its ethanol extract (Aa-EE) under various photoaging conditions using skin-originated cells, and the underlying mechanism was also examined using various types of cells.

MATERIALS AND METHODS

Effects of Aa-EE on cell viability, photocytotoxicity, and expression of matrix metalloproteinases (MMPs), cyclooxygenase (COX)-2, and moisturizing factors were measured in B16F10, HEK293, NIH3T3, and HaCaT cells under untreated and ultraviolet B (UVB)-irradiation conditions. Anti-melanogenic effect of Aa-EE was also examined by measuring both melanin content in B16F10 cells and tyrosinase activity. Anti-photoaging mechanism of Aa-EE was explored by determining the activation levels of signaling molecules by immunoblotting analysis.

RESULTS

Aa-EE protected HaCaT cells from UVB irradiation-induced death. Aa-EE increased the expression of a type 1 pro-collagen gene and decreased the expression of matrix metalloproteinases, and COX-2 in NIH3T3 cells induced by UVB. Aa-EE increased the expression of transglutamase-1, hyaluronic acid synthase (HAS)-2, and HAS-3 in HaCaT cells and decreased the production of melanin in α-melanocyte-stimulating hormone-stimulated B16F10 cells by suppressing tyrosinase activity and the expression of tyrosinase, microphthalmia-associated transcription factor, tyrosinase-related protein (TRP)-1 and TRP-2.

CONCLUSION

The results suggest that Aa-EE could be skin-protective remedy with anti-photoaging, anti-apoptotic, skin remodeling, moisturizing, and anti-melanogenesis properties.

摘要

植物药相关性

青蒿是一种传统的草本植物,长期以来一直被用于抗炎、抗感染和皮肤保护疗法。

研究目的

本研究采用皮肤源性细胞,在各种光老化条件下,对青蒿传统上已知的皮肤保护活性进行了研究,并利用各种类型的细胞对其潜在机制进行了研究。

材料和方法

在未经紫外线 B(UVB)照射和 UVB 照射条件下,用 B16F10、HEK293、NIH3T3 和 HaCaT 细胞测量青蒿乙醇提取物(Aa-EE)对细胞活力、光细胞毒性以及基质金属蛋白酶(MMPs)、环氧化酶(COX)-2 和保湿因子表达的影响。还通过测量 B16F10 细胞中的黑色素含量和酪氨酸酶活性来检查 Aa-EE 的抗黑色素生成作用。通过免疫印迹分析确定信号分子的激活水平,探讨 Aa-EE 的抗光老化机制。

结果

Aa-EE 可保护 HaCaT 细胞免受 UVB 照射诱导的死亡。Aa-EE 增加了 NIH3T3 细胞中由 UVB 诱导的Ⅰ型前胶原基因的表达,降低了 MMPs 和 COX-2 的表达。Aa-EE 增加了 HaCaT 细胞中转谷氨酰胺酶-1、透明质酸合酶(HAS)-2 和 HAS-3 的表达,并通过抑制酪氨酸酶活性和酪氨酸酶、小眼畸形相关转录因子、酪氨酸酶相关蛋白(TRP)-1 和 TRP-2 的表达,减少了α-促黑素细胞刺激素刺激的 B16F10 细胞中黑色素的产生。

结论

结果表明,Aa-EE 可能是一种具有抗光老化、抗凋亡、皮肤重塑、保湿和抗黑色素生成作用的皮肤保护疗法。

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