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In silico analysis of Pers. phytocompounds against wound healing biomarkers and ascertaining through in vitro cell migration assay.对Pers.植物化合物进行计算机模拟分析,研究其对伤口愈合生物标志物的作用,并通过体外细胞迁移试验进行验证。
3 Biotech. 2022 Aug;12(8):166. doi: 10.1007/s13205-022-03229-9. Epub 2022 Jul 11.
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本文引用的文献

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The Wound Healing Potential of (Pers.) C. D. Adams (Asteraceae).(波斯)C.D.亚当斯(菊科)的伤口愈合潜力
Evid Based Complement Alternat Med. 2019 Jan 21;2019:7957860. doi: 10.1155/2019/7957860. eCollection 2019.
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Synthesis, Biological Evaluation and Molecular Docking Studies of New Pyrazolines as an Antitubercular and Cytotoxic Agents.新型吡唑啉类抗结核和细胞毒性药物的合成、生物学评价及分子对接研究
Infect Disord Drug Targets. 2019;19(3):310-321. doi: 10.2174/1871526519666181217120626.
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Chemical Composition and Antifungal and , Antioxidant, and Anticholinesterase Activities of Extracts and Constituents of (DC.) Baill.(DC.)贝利提取物及其成分的化学成分、抗真菌、抗氧化和抗胆碱酯酶活性
Evid Based Complement Alternat Med. 2018 Nov 7;2018:1748487. doi: 10.1155/2018/1748487. eCollection 2018.
4
Induction of Colonic Regulatory T Cells by Mesalamine by Activating the Aryl Hydrocarbon Receptor.美沙拉嗪通过激活芳烃受体诱导结肠调节性T细胞
Cell Mol Gastroenterol Hepatol. 2017 Apr 11;4(1):135-151. doi: 10.1016/j.jcmgh.2017.03.010. eCollection 2017 Jul.
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Receptor-ligand molecular docking.受体-配体分子对接
Biophys Rev. 2014 Mar;6(1):75-87. doi: 10.1007/s12551-013-0130-2. Epub 2013 Dec 21.
6
Ex Vivo Application of Secreted Metabolites Produced by Soil-Inhabiting Bacillus spp. Efficiently Controls Foliar Diseases Caused by Alternaria spp.土壤芽孢杆菌属产生的分泌代谢产物的体外应用可有效控制链格孢属引起的叶部病害
Appl Environ Microbiol. 2015 Oct 30;82(2):478-90. doi: 10.1128/AEM.02662-15. Print 2016 Jan 15.
7
Wound repair and regeneration: mechanisms, signaling, and translation.伤口修复与再生:机制、信号传导及转化应用
Sci Transl Med. 2014 Dec 3;6(265):265sr6. doi: 10.1126/scitranslmed.3009337.
8
Advances in skin grafting and treatment of cutaneous wounds.皮肤移植和皮肤伤口治疗的进展。
Science. 2014 Nov 21;346(6212):941-5. doi: 10.1126/science.1253836.
9
Innate and Adaptive Immune Responses in Wound Epithelialization.伤口上皮化过程中的先天性和适应性免疫反应
Adv Wound Care (New Rochelle). 2014 Jul 1;3(7):492-501. doi: 10.1089/wound.2012.0435.
10
Computational Modeling of Inflammation and Wound Healing.炎症与伤口愈合的计算建模
Adv Wound Care (New Rochelle). 2013 Nov;2(9):527-537. doi: 10.1089/wound.2012.0416.

对Pers.植物化合物进行计算机模拟分析,研究其对伤口愈合生物标志物的作用,并通过体外细胞迁移试验进行验证。

In silico analysis of Pers. phytocompounds against wound healing biomarkers and ascertaining through in vitro cell migration assay.

作者信息

Saha Shraddha, Naik Jinal, Amaresan Natarajan, Pithawala Meonis

机构信息

C. G. Bhakta Institute of Biotechnology, Uka Tarsadia University, Maliba Campus, Bardoli, Surat, Gujarat 394350 India.

出版信息

3 Biotech. 2022 Aug;12(8):166. doi: 10.1007/s13205-022-03229-9. Epub 2022 Jul 11.

DOI:10.1007/s13205-022-03229-9
PMID:35845110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9276916/
Abstract

Pers. is known for its medicinal properties. Although traditionally Pers. has been used for wound healing, yet scientific investigations reporting its ability to heal wounds are lacking. Phytochemical profiling of Pers. inflorescence crude extract was carried out by LC-MS analysis. Ten phytochemicals were selected for in silico analysis based on retention time, mass-to-charge ratio and resolution of mass spectrum. Molecular docking of all ten compounds was done against selected wound healing biomarkers viz., interleukin 6(IL-6), interleukin β (IL-β), insulin-like growth factor tyrosine kinase receptor (IGF-1R) and transformation growth factor β (TGF-β). Based on this, catechin, mesalazine and piperazine were subjected for in vitro cell migration assay (3T3 L1 mouse fibroblast cell line) to assess their wound healing potentials. Molecular docking revealed that mesalazine, catechin, and piperazine have potential ligands based on lowest docking energy (ranging from - 4.1587 to - 0.972), Glide E score (ranging from - 26.929 to - 57.882), Glide G score (ranging from - 4.16 to - 7.972) and numbers of hydrogen bonds compared to other compounds studied. The migration assay revealed that, compared to control (52.5%), Pers. inflorescence crude extract showed maximum wound healing potential (80%) followed by Catechin (66.8%) Mesalazine (58.3%) and Piperazine (51.2%). The combined in silico and in vitro approach opens new dimension for designing innovative therapeutics to manage different types of wounds.

摘要

Pers.因其药用特性而闻名。尽管传统上Pers.一直用于伤口愈合,但缺乏报告其伤口愈合能力的科学研究。通过液相色谱-质谱分析对Pers.花序粗提物进行了植物化学分析。根据保留时间、质荷比和质谱分辨率选择了10种植物化学物质进行计算机模拟分析。对所有10种化合物与选定的伤口愈合生物标志物即白细胞介素6(IL-6)、白细胞介素β(IL-β)、胰岛素样生长因子酪氨酸激酶受体(IGF-1R)和转化生长因子β(TGF-β)进行了分子对接。基于此,对儿茶素、美沙拉嗪和哌嗪进行体外细胞迁移试验(3T3 L1小鼠成纤维细胞系)以评估它们的伤口愈合潜力。分子对接显示,与其他研究的化合物相比,美沙拉嗪、儿茶素和哌嗪具有基于最低对接能量(范围为-4.1587至-0.972)、Glide E分数(范围为-26.929至-57.882)、Glide G分数(范围为-4.16至-7.972)和氢键数量的潜在配体。迁移试验表明,与对照(52.5%)相比,Pers.花序粗提物显示出最大的伤口愈合潜力(80%),其次是儿茶素(66.8%)、美沙拉嗪(58.3%)和哌嗪(51.2%)。计算机模拟和体外相结合的方法为设计创新疗法来治疗不同类型的伤口开辟了新的维度。