放线菌水提取物(APWE)通过 MAPK/AP-1 和 TGFβ-Smad 通路防止紫外线诱导的光老化

Jung Min Lee, Su-Jin Park, Yu-Jin Kim, Su-Young Kim, Yoo-Na Jang, A Yeon Park, Seong-Hyun Ho, Dayoung Kim, Jung Ok Lee, Kwang-Ho Yoo, Beom Joon Kim
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Type I collagen, matrix metalloproteinase-1 (MMP-1), tissue inhibitor of metalloproteinase (TIMP-1), hyaluronic acid (HA), hyaluronan synthase 1 (HAS1) and HAS2 levels were measuring by enzyme-linked immunosorbent assay or reverse transcription quantitative polymerase chain reaction. Also, we investigate the effects of PB203 on wrinkle formation, and the potential mechanisms underlying such effects were investigated in UVB-induced wrinkle mouse model mice.</p><p><strong>Results: </strong>PB203 alleviated the UVB-induced reactive oxygen species production, phosphorylation of JNK, ERK, and p38, and formation of AP-1. In addition, PB203 inhibited the decreases in type I collagen and TIMP-1 levels, and the increase in MMP-1 levels in UVB-exposed HaCaT cells. In UVB-induced wrinkle mouse model, PB203 inhibited the decreases in elastin and type I collagen levels as well as the increases in MMP-1 expression, wrinkle formation, and skin dehydration. 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引用次数: 0

摘要

背景:银藤在东方医学中被用于治疗痛风、类风湿性关节炎和炎症。Actinidia polygama 水提取物(APWE)被命名为 PB203:研究 PB203 是否具有抗光老化作用,并了解这种作用的分子机制:方法:采用 1,1-二苯基-2-苦基肼检测法和 2',7'-二氯二氢荧光素二乙酸染色法评估经紫外线 B(UVB)照射的 HaCaT 细胞在处理或未处理 PB203 的情况下的抗氧化效果。通过酶联免疫吸附试验或逆转录定量聚合酶链反应测定 I 型胶原、基质金属蛋白酶-1 (MMP-1)、金属蛋白酶组织抑制剂 (TIMP-1)、透明质酸 (HA)、透明质酸合成酶 1 (HAS1) 和 HAS2 的水平。此外,我们还研究了 PB203 对皱纹形成的影响,并在紫外线诱导的皱纹小鼠模型中研究了这种影响的潜在机制:结果:PB203能缓解紫外线诱导的活性氧生成、JNK、ERK和p38的磷酸化以及AP-1的形成。此外,PB203 还能抑制 UVB 暴露的 HaCaT 细胞中 I 型胶原蛋白和 TIMP-1 水平的降低以及 MMP-1 水平的升高。在紫外线诱导的皱纹小鼠模型中,PB203 可抑制弹性蛋白和 I 型胶原蛋白水平的降低以及 MMP-1 表达的增加、皱纹的形成和皮肤脱水。此外,PB203 还能增加丝胶蛋白、HAS1 和 HAS2 的表达,改善皮肤屏障功能:综上所述,我们发现 PB203 是一种有效的候选功能成分或治疗剂,可用于改善紫外线介导的皮肤老化。
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Actinidia polygama Water Extract (APWE) Protects Against UVB-Induced Photoaging via MAPK/AP-1 and TGFβ-Smad Pathway.

Background: Actinidia polygama (silver vine) has been used in oriental medicine to treat gout, rheumatoid arthritis, and inflammation. Actinidia polygama water extract (APWE) is named PB203.

Objective: To investigate whether PB203 has anti-photoaging effects and to understand the molecular mechanism underlying such effects.

Methods: The antioxidant effect was assessed by 1,1-diphenyl-2-picrylhydrazyl assay and 2',7'-dichlorodihydrofluorescein diacetate staining in ultraviolet B (UVB)-irradiated HaCaT cells with or without PB203 treatment. Type I collagen, matrix metalloproteinase-1 (MMP-1), tissue inhibitor of metalloproteinase (TIMP-1), hyaluronic acid (HA), hyaluronan synthase 1 (HAS1) and HAS2 levels were measuring by enzyme-linked immunosorbent assay or reverse transcription quantitative polymerase chain reaction. Also, we investigate the effects of PB203 on wrinkle formation, and the potential mechanisms underlying such effects were investigated in UVB-induced wrinkle mouse model mice.

Results: PB203 alleviated the UVB-induced reactive oxygen species production, phosphorylation of JNK, ERK, and p38, and formation of AP-1. In addition, PB203 inhibited the decreases in type I collagen and TIMP-1 levels, and the increase in MMP-1 levels in UVB-exposed HaCaT cells. In UVB-induced wrinkle mouse model, PB203 inhibited the decreases in elastin and type I collagen levels as well as the increases in MMP-1 expression, wrinkle formation, and skin dehydration. Furthermore, PB203 increased the expression of filaggrin, HAS1, and HAS2, improving the skin barrier function.

Conclusion: Taken together, we found that PB203 is as a potent candidate to serve as a functional ingredient or therapeutic agent to improve UVB-mediated skin aging.

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