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基于结构的药物设计和鉴定辣木抑制剂,针对热休克蛋白 (HSP70-1) 作为咪喹莫特诱导的小鼠银屑病样皮肤炎症的抑制剂。

Structure-based drug designing and identification of Woodfordia fruticosa inhibitors targeted against heat shock protein (HSP70-1) as suppressor for Imiquimod-induced psoriasis like skin inflammation in mice model.

机构信息

Molecular Microbiology Laboratory, Biotechnology Department, Indian Institute of Technology, Roorkee 247667, Uttarakhand, India.

Bioinformatics Division, Indian Institute of Information Technology, Allahabad 211012, Uttar Pradesh, India.

出版信息

Mater Sci Eng C Mater Biol Appl. 2019 Feb 1;95:57-71. doi: 10.1016/j.msec.2018.10.061. Epub 2018 Oct 19.

Abstract

Heat shock proteins (HSPs) emerged as a therapeutic target and it was observed that inhibition of HSP70-1 plays a pivotal role in the management of psoriasis. In-silico investigation involving techniques like molecular docking and molecular dynamics (MD) simulation analysis was performed against HSP70-1. Further, anti-psoriatic activity of bioactive immunomodulatory compounds present in ethanolic extract of Woodfordia fruticosa flowers (Wffe) using combination of bioinformatics together with ethnopharmacological approach has been explored in this study. Myricetin (-8.024), Quercetin (-7.368) and Ellagic acid (-7.311) were the top three compounds with minimum energy levels as well as high therapeutic value/ADMET as compared to currently available marketed anti-psoriatic drug Tretinoin (-7.195). ADMET prediction was used to screen ligands for drug-likeness and efficacy. Further, biogenically Woodfordia fruticosa gold nanoparticles (WfAuNPs) were synthesized and characterized by UV-Visible Spectroscopy (UV-vis), Dynamic Light Scattering (DLS), Zeta Potential, X-Ray Diffraction (XRD) and High Resolution Transmission Electron Microscopy (HRTEM) techniques. Synthesized WfAuNPs observed in the size range of 10-20 nm and were used to develop WfAuNPs-Carbopol®934 ointment gel. Subsequently, the therapeutic efficacy of WfAuNPs-Carbopol® 934 was checked against 5% Imiquimod-induced psoriasis like skin inflammation. WfAuNPs-Carbopol® 934 was found to be exerting better therapeutic effect in reducing the mean DAI score (0.63 ± 0.08), serum cytokines (TNF-α, IL-22 and IL-23) levels along with reduced epidermal thickness, parakeratosis and marked decrease in the hyperproliferation of keratinocytes. Results of the study revealed that the WfAuNPs-Carbopol® 934 could be an effective alternative treatment for psoriasis in near future.

摘要

热休克蛋白(HSPs)成为治疗靶点,研究发现抑制 HSP70-1 在治疗银屑病中起着关键作用。本研究采用分子对接和分子动力学(MD)模拟分析等技术对 HSP70-1 进行了计算机研究。此外,本研究还结合生物信息学和民族药理学方法,研究了辣木花(Wffe)乙醇提取物中具有免疫调节作用的生物活性化合物对银屑病的抗作用。与现有的市售抗银屑病药物维甲酸(Tretinoin)相比,杨梅素(-8.024)、槲皮素(-7.368)和鞣花酸(-7.311)是能量最低、治疗价值/ADMET 最高的前三种化合物。ADMET 预测用于筛选具有药物相似性和疗效的配体。此外,还合成并通过紫外可见分光光度法(UV-vis)、动态光散射(DLS)、Zeta 电位、X 射线衍射(XRD)和高分辨率透射电子显微镜(HRTEM)技术对生物合成的辣木叶金纳米粒子(WfAuNPs)进行了表征。合成的 WfAuNPs 的尺寸范围为 10-20nm,并用于开发 WfAuNPs-Carbopol®934 软膏凝胶。随后,检查了 WfAuNPs-Carbopol®934 对 5%咪喹莫特诱导的银屑病样皮肤炎症的治疗效果。结果发现,WfAuNPs-Carbopol®934 能更好地降低平均 DAI 评分(0.63±0.08)、血清细胞因子(TNF-α、IL-22 和 IL-23)水平,减少表皮厚度、角化不全和角蛋白细胞过度增殖。研究结果表明,WfAuNPs-Carbopol®934 可能成为未来治疗银屑病的有效替代方法。

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