In Silico Screening, In Vitro Mpro Inhibitory, and Adjunctive Therapy Value of Minocycline for the Treatment of COVID-19

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Journal of Clinical Pharmacy and Therapeutics Pub Date : 2023-10-09 DOI:10.1155/2023/9955105
Yaru Han, Xianxiang Bai, Si Wu, Xiurong Luan, Liwen Ren, Jinhua Wang, Zhanfei She, Bin Xiao, Guanhua Du
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Abstract

What Is Known and Objective. Novel coronavirus disease (COVID-19) is still ravaging globally since its first discovery in 2019. With the continuous emergence of severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) mutant strains, therapeutic entities are still needed to be discovered. This study was to explore SARS-CoV-2 inhibitors and therapeutic entities for COVID-19. Methods. Based on Lipinski’s rule of 5, a small-scale “old” drug database (clinical drugs being used in Ordos Central Hospital) was established, and in silico screening of Mpro inhibitors was conducted. Binding affinity and interaction as well as structure-affinity relationship were analyzed. Furthermore, molecular dynamic (MD) simulation of the selected drugs was performed to understand the conformational changes in docked complex. In vitro Mpro inhibition tests were performed according to established methods. Finally, literature review of potential “old” drug for the treatment of COVID-19 was conducted. Results and Discussion. The antibiotic minocycline, an inhibitor of bacterial ribosomal RNA, was screened out which showed the highest binding affinity (−9.6 kcal/mol). Beside the hydrogen bond with Cys145 and hydrophobic interactions, minocycline formed a pi-cation with His41, which strongly supported minocycline as a Michael addition acceptor to bind with the catalytic site of Mpro. MD simulation results show that minocycline displayed less conformational changes. The structure-affinity relationship was summarized based on minocycline analogs, and minocycline showed in vitro Mpro inhibitory activity with IC50 of 5 mM. More importantly, the literature review found that minocycline had both in vitro and in vivo broad-spectrum antiviral as well as anti-inflammatory activities, and the levels of a broad spectrum of biological markers during minocycline administration were opposed to those of COVID-19 conditions (both severe and nonsevere). What is New and Conclusion. Minocycline deserves an adjunctive therapeutic option for COVID-19 condition (both severe and nonsevere). This study shed a new light on drug-repurposing strategy for the viral disease.
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米诺环素体外Mpro抑制及辅助治疗COVID-19的价值
已知的和客观的。新型冠状病毒病(COVID-19)自2019年首次发现以来,仍在全球肆虐。随着严重急性呼吸综合征-冠状病毒-2 (SARS-CoV-2)突变株的不断出现,仍需寻找治疗实体。本研究旨在探索SARS-CoV-2抑制剂和COVID-19治疗实体。方法。基于Lipinski的5法则,建立小规模“老”药物数据库(鄂尔多斯中心医院临床使用的药物),对Mpro抑制剂进行计算机筛选。分析了它们的结合亲和力、相互作用以及结构亲和力关系。此外,对所选药物进行分子动力学(MD)模拟,了解对接物的构象变化。根据建立的方法进行体外Mpro抑制试验。最后,对治疗COVID-19的潜在“老”药物进行了文献综述。结果和讨论。筛选出细菌核糖体RNA抑制剂米诺环素(minocycline),其结合亲和力最高(- 9.6 kcal/mol)。除了与Cys145的氢键和疏水相互作用外,米诺环素与His41形成了一个π -阳离子,这有力地支持了米诺环素作为Michael加成受体与Mpro的催化位点结合。MD模拟结果表明,米诺环素的构象变化较小。基于米诺环素类似物的结构-亲和关系进行总结,米诺环素显示出体外Mpro抑制活性,IC50为5 mM。更重要的是,文献综述发现米诺环素具有体外和体内广谱抗病毒和抗炎活性,并且米诺环素给药期间广谱生物标志物水平与COVID-19病情(严重和非严重)相反。什么是新的和结论。二甲胺四环素值得作为COVID-19病情(严重和非严重)的辅助治疗选择。这项研究为这种病毒性疾病的药物再利用策略提供了新的思路。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
226
审稿时长
6 months
期刊介绍: The Journal of Clinical Pharmacy and Therapeutics provides a forum for clinicians, pharmacists and pharmacologists to explore and report on issues of common interest. Reports and commentaries on current issues in medical and pharmaceutical practice are encouraged. Papers on evidence-based clinical practice and multidisciplinary collaborative work are particularly welcome. Regular sections in the journal include: editorials, commentaries, reviews (including systematic overviews and meta-analyses), original research and reports, and book reviews. Its scope embraces all aspects of clinical drug development and therapeutics, including: Rational therapeutics Evidence-based practice Safety, cost-effectiveness and clinical efficacy of drugs Drug interactions Clinical impact of drug formulations Pharmacogenetics Personalised, stratified and translational medicine Clinical pharmacokinetics.
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