Suppr超能文献

局部用制剂中加入查尔酮可抑制无毛小鼠紫外线 B 辐射皮肤损伤模型中的皮肤炎症和氧化应激。

Trans-chalcone added in topical formulation inhibits skin inflammation and oxidative stress in a model of ultraviolet B radiation skin damage in hairless mice.

机构信息

Departamento de Ciências Farmacêuticas, Universidade Estadual de Londrina, Avenida Robert Koch, 60, Hospital Universitário, 86039-440 Londrina, Paraná, Brazil.

Departamento de Ciências Patológicas, Universidade Estadual de Londrina, Rodovia Celso Garcia Cid, Km 380, PR445, Cx. Postal 10.011, 86057-970 Londrina, Paraná, Brazil.

出版信息

J Photochem Photobiol B. 2017 Jun;171:139-146. doi: 10.1016/j.jphotobiol.2017.05.002. Epub 2017 May 2.

Abstract

Trans-chalcone (TC) is a common precursor of flavonoids. However, the pharmacological properties of TC remain to be fully understood. The present study investigated whether topical formulation containing TC (TFcTC) presents therapeutic effect in UVB radiation-induced skin damage using disease, enzyme activity, antioxidant activity, protein and mRNA parameters. Control topical formulation (CTF) and TFcTC were applied in hairless mice before and after exposure to UVB radiation. Dorsal skin samples were collected after UVB exposure to evaluate: i) skin edema (weight) was measured by punch biopsy; ii) spectrophotometric assays were used to measure myeloperoxidase (MPO) and catalase activities, ferric (FRAP) and ABTS cation reducing antioxidant power, superoxide anion production and levels of reduced glutathione (GSH); iii) enzymography was used to measure matrix metalloproteinase-9 (MMP-9) activity; iv) chemiluminescence was used to measure the lipid peroxidation (LPO); v) enzyme-linked immunosorbent assay (ELISA) was used to measure tumor necrosis factor alpha (TNF-α) levels; vi) reverse transcription quantitative PCR (RT-qPCR) was used to measure cyclooxygenase-2 (COX-2), gp91 (NADPH oxidase sub-unity), glutathione peroxidase-1 (Gpx1), glutathione reductase (Gr), nuclear factor erythroid 2-related factor 2 (Nrf2), and heme oxygenase-1 (HO-1) mRNA expression. TFcTC inhibited UVB-induced skin edema, MPO activity, MMP-9 activity, TNF-α production, and COX-2 mRNA expression. TFcTC inhibited UVB-induced LPO, down-regulated superoxide anion levels and gp91 mRNA expression, and improved antioxidant potential and GSH skin levels. The mRNA expression of detoxification systems such as Nrf2, HO-1, Gpx1 and Gr, and catalase activity were also enhanced by treatment with TFcTC. In conclusion, TFcTC protects mice skin from UVB radiation by inhibiting inflammation, and improving antioxidant and detoxification systems. Therefore, topical treatment with TC is a novel therapeutic approach for the treatment of UVB radiation skin damages, which merits further pre-clinical and clinical investigation.

摘要

反式查耳酮(TC)是类黄酮的常见前体。然而,TC 的药理作用仍有待充分了解。本研究通过疾病、酶活性、抗氧化活性、蛋白质和 mRNA 参数,探讨了含有 TC 的局部制剂(TFcTC)是否对 UVB 辐射诱导的皮肤损伤具有治疗作用。在暴露于 UVB 辐射之前和之后,将对照局部制剂(CTF)和 TFcTC 应用于无毛小鼠。在暴露于 UVB 后采集背部皮肤样本以评估:i)通过打孔活检测量皮肤水肿(重量);ii)使用分光光度法测定髓过氧化物酶(MPO)和过氧化氢酶活性、铁(FRAP)和 ABTS 阳离子还原抗氧化能力、超氧阴离子产生和还原型谷胱甘肽(GSH)水平;iii)酶谱法测定基质金属蛋白酶-9(MMP-9)活性;iv)化学发光法测定脂质过氧化(LPO);v)酶联免疫吸附测定(ELISA)测定肿瘤坏死因子-α(TNF-α)水平;vi)逆转录定量 PCR(RT-qPCR)测定环氧化酶-2(COX-2)、gp91(NADPH 氧化酶亚单位)、谷胱甘肽过氧化物酶-1(Gpx1)、谷胱甘肽还原酶(Gr)、核因子红细胞 2 相关因子 2(Nrf2)和血红素加氧酶-1(HO-1)mRNA 表达。TFcTC 抑制 UVB 诱导的皮肤水肿、MPO 活性、MMP-9 活性、TNF-α 产生和 COX-2 mRNA 表达。TFcTC 抑制 UVB 诱导的 LPO,下调超氧阴离子水平和 gp91 mRNA 表达,并改善抗氧化能力和 GSH 皮肤水平。解毒系统如 Nrf2、HO-1、Gpx1 和 Gr 的 mRNA 表达以及过氧化氢酶活性也因 TFcTC 的治疗而增强。总之,TFcTC 通过抑制炎症和改善抗氧化和解毒系统来保护小鼠皮肤免受 UVB 辐射。因此,TC 的局部治疗是治疗 UVB 辐射皮肤损伤的一种新的治疗方法,值得进一步进行临床前和临床研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验