Suppr超能文献

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.

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。

相似文献

7
Biofilm inhibition mechanism from extract of Hymenocallis littoralis leaves.沿阶草叶提取物的抑菌机制。
J Ethnopharmacol. 2018 Aug 10;222:121-132. doi: 10.1016/j.jep.2018.04.031. Epub 2018 Apr 24.

本文引用的文献

1
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.
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.
5
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.
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.

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