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非酶促软化樱花提取物对日光紫外线诱导的基质金属蛋白酶(MMP)-1表达的抑制作用

Inhibition of Solar UV-Induced Matrix Metalloproteinase (MMP)-1 Expression by Non-Enzymatic Softening Cherry Blossom () Extract.

作者信息

Jung Yeong-A, Lee Ji-Yoon, Lee Pomjoo, Shin Han-Seung, Kim Jong-Eun

机构信息

Department of Food Science and Biotechnology, Dongguk University-Seoul, Ilsandong-gu, Goyang-si 10326, Korea.

Biomodulation Major, Department of Agricultural Biotechnology, Seoul National University, Seoul 08826, Korea.

出版信息

Plants (Basel). 2021 May 19;10(5):1016. doi: 10.3390/plants10051016.

Abstract

Cherry blossom () petals are used as ingredients in many cosmetics. However, despite their use in numerous products, the exact function of cherry blossom petals in cosmetics is unclear. Therefore, we need evidence-based studies to support the labeling claims that are made in cherry blossom products in the cosmetics industry. We investigated the skin anti-aging potential of non-enzymatic softening cherry blossom extract (NES-CBE) in this study. The extract desalinated, to improve its quality such that it can be used as a functional material for the skin. The anti-wrinkle effect of NES-CBE was investigated on human keratinocytes (HaCaT cells) under solar UV (sUV) light exposure. We found that NES-CBE reduced the sUV-induced matrix metalloproteinase (MMP)-1 expression and modulated the transactivation of the activator protein (AP)-1. Furthermore, NES-CBE suppressed the phosphorylation of MEK1/2 and ERK proteins, indicating its regulation of sUV-induced MAPK signaling. Additionally, we observed NES-CBE reduced MMP-1 protein expression in a human skin equivalent model. Taken together, these results suggest that NES-CBE reduces sUV-induced MMP-1 protein expression through reducing AP-1 transactivation via regulation of the MEK1/2-ERK pathway.

摘要

樱花()花瓣被用作许多化妆品的成分。然而,尽管它们被用于众多产品中,但樱花花瓣在化妆品中的具体功能尚不清楚。因此,我们需要基于证据的研究来支持化妆品行业中樱花产品所做的标签声明。在本研究中,我们调查了非酶促软化樱花提取物(NES-CBE)的皮肤抗衰老潜力。对提取物进行脱盐处理,以提高其质量,使其能够用作皮肤的功能性材料。在太阳紫外线(sUV)照射下,研究了NES-CBE对人角质形成细胞(HaCaT细胞)的抗皱作用。我们发现NES-CBE降低了sUV诱导的基质金属蛋白酶(MMP)-1表达,并调节了激活蛋白(AP)-1的反式激活。此外,NES-CBE抑制了MEK1/2和ERK蛋白的磷酸化,表明其对sUV诱导的MAPK信号通路的调节作用。此外,我们观察到NES-CBE在人皮肤等效模型中降低了MMP-1蛋白表达。综上所述,这些结果表明NES-CBE通过调节MEK1/2-ERK途径减少AP-1反式激活,从而降低sUV诱导的MMP-1蛋白表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fbc/8161269/f526d0440e65/plants-10-01016-g001.jpg

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