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红景天苷可以靶向 P4HB 介导的炎症和皮肤的黑色素生成。

Salidroside can target both P4HB-mediated inflammation and melanogenesis of the skin.

机构信息

Cheermore Cosmetic Dermatology Laboratory, Shanghai, China.

State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai University, Tianjin, China.

出版信息

Theranostics. 2020 Aug 13;10(24):11110-11126. doi: 10.7150/thno.47413. eCollection 2020.

Abstract

Many external factors can induce the melanogenesis and inflammation of the skin. Salidroside (SAL) is the main active ingredient of , which is a perennial grass plant of the Family Crassulaceae. This study evaluated the effect and molecular mechanism of SAL on skin inflammation and melanin production. It then explored the molecular mechanism of melanin production under ultraviolet (UV) and inflammatory stimulation. VISIA skin analysis imaging system and DermaLab instruments were used to detect the melanin reduction and skin brightness improvement rate of the volunteers. UV-treated Kunming mice were used to detect the effect of SAL on skin inflammation and melanin production. Molecular docking and Biacore were used to verify the target of SAL. Immunofluorescence, luciferase reporter assay, CO-IP, pull-down, Western blot, proximity ligation assay (PLA), and qPCR were used to investigate the molecular mechanism by which SAL regulates skin inflammation and melanin production. SAL can inhibit the inflammation and melanin production of the volunteers. SAL also exerted a protective effect on the UV-treated Kunming mice. SAL can inhibit the tyrosinase (TYR) activity and TYR mRNA expression in A375 cells. SAL can also regulate the ubiquitination degradation of interferon regulatory factor 1 (IRF1) by targeting prolyl 4-hydroxylase beta polypeptide (P4HB) to mediate inflammation and melanin production. This study also revealed that IRF1 and upstream stimulatory factor 1 (USF1) can form a transcription complex to regulate TYR mRNA expression. IRF1 also mediated inflammatory reaction and TYR expression under UV- and lipopolysaccharide-induced conditions. Moreover, SAL derivative SAL-plus (1-(3,5-dihydroxyphenyl) ethyl-β-d-glucoside) showed better effect on inflammation and melanin production than SAL. SAL can inhibit the inflammation and melanogenesis of the skin by targeting P4HB and regulating the formation of the IRF1/USF1 transcription complex. In addition, SAL-plus may be a new melanin production and inflammatory inhibitor.

摘要

许多外部因素可诱导皮肤的黑色素生成和炎症反应。红景天苷(SAL)是景天属植物的主要活性成分,景天属植物是景天科的一种多年生草本植物。本研究评估了 SAL 对皮肤炎症和黑色素生成的影响及其分子机制,并探讨了在紫外线(UV)和炎症刺激下黑色素生成的分子机制。VISIA 皮肤分析成像系统和 DermaLab 仪器用于检测志愿者的黑色素减少和皮肤亮度提高率。使用 UV 处理的昆明小鼠检测 SAL 对皮肤炎症和黑色素生成的影响。分子对接和 Biacore 用于验证 SAL 的靶标。免疫荧光、荧光素酶报告基因检测、CO-IP、下拉实验、Western blot、临近连接分析(PLA)和 qPCR 用于研究 SAL 调节皮肤炎症和黑色素生成的分子机制。SAL 可抑制志愿者的炎症和黑色素生成。SAL 对 UV 处理的昆明小鼠也具有保护作用。SAL 可抑制 A375 细胞中的酪氨酸酶(TYR)活性和 TYR mRNA 表达。SAL 还可以通过靶向脯氨酰 4-羟化酶β多肽(P4HB)调节干扰素调节因子 1(IRF1)的泛素化降解,从而调节炎症和黑色素生成。本研究还揭示了 IRF1 和上游刺激因子 1(USF1)可以形成转录复合物来调节 TYR mRNA 表达。IRF1 还介导 UV 和脂多糖诱导条件下的炎症反应和 TYR 表达。此外,SAL 衍生物 SAL-plus(1-(3,5-二羟基苯基)乙基-β-D-葡萄糖苷)在炎症和黑色素生成方面的效果优于 SAL。SAL 可通过靶向 P4HB 抑制皮肤炎症和黑色素生成,并调节 IRF1/USF1 转录复合物的形成。此外,SAL-plus 可能是一种新的黑色素生成和炎症抑制剂。

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