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甘氨酰化二甲双胍治疗可降低 SARS-CoV-2 病毒载量:一项体外模型和随机、双盲、IIb 期临床试验。

Treatment with metformin glycinate reduces SARS-CoV-2 viral load: An in vitro model and randomized, double-blind, Phase IIb clinical trial.

机构信息

Departamento de Innovación Biomédica, CICESE, Carretera Ensenada-Tijuana 3918, Zona Playitas, Ensenada, BC 22860, Mexico.

The American British Cowdray Medical Center I.A.P. (Centro Médico ABC), Mexico.

出版信息

Biomed Pharmacother. 2022 Aug;152:113223. doi: 10.1016/j.biopha.2022.113223. Epub 2022 Jun 2.

DOI:10.1016/j.biopha.2022.113223
PMID:35709650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9159967/
Abstract

The health crisis caused by the new coronavirus SARS-CoV-2 highlights the need to identify new treatment strategies for this viral infection. During the past year, over 400 coronavirus disease (COVID-19) treatment patents have been registered; nevertheless, the presence of new virus variants has triggered more severe disease presentations and reduced treatment effectiveness, highlighting the need for new treatment options for the COVID-19. This study evaluates the Metformin Glycinate (MG) effect on the SARS-CoV-2 in vitro and in vivo viral load. The in vitro study was conducted in a model of Vero E6 cells, while the in vivo study was an adaptive, two-armed, randomized, prospective, longitudinal, double-blind, multicentric, and phase IIb clinical trial. Our in vitro results revealed that MG effectively inhibits viral replication after 48 h of exposure to the drug, with no cytotoxic effect in doses up to 100 µM. The effect of the MG was also tested against three variants of interest (alpha, delta, and epsilon), showing increased survival rates in cells treated with MG. These results are aligned with our clinical data, which indicates that MG treatment reduces SARS-CoV2-infected patients´ viral load in just 3.3 days and supplementary oxygen requirements compared with the control group. We expect our results can guide efforts to position MG as a therapeutic option for COVID-19 patients.

摘要

由新型冠状病毒 SARS-CoV-2 引起的健康危机凸显了确定针对这种病毒感染的新治疗策略的必要性。在过去的一年中,已经有超过 400 项冠状病毒病 (COVID-19) 治疗专利被注册;然而,新病毒变种的出现引发了更严重的疾病表现,并降低了治疗效果,突出了需要为 COVID-19 提供新的治疗选择。本研究评估了甘氨酸甲福明 (MG) 对 SARS-CoV-2 的体外和体内病毒载量的影响。体外研究在 Vero E6 细胞模型中进行,而体内研究是一项适应性、双臂、随机、前瞻性、纵向、双盲、多中心、IIb 期临床试验。我们的体外结果表明,MG 在暴露于药物 48 小时后能有效抑制病毒复制,在高达 100 μM 的剂量下没有细胞毒性作用。MG 的作用还针对三种关注变体(alpha、delta 和 epsilon)进行了测试,结果表明在 MG 处理的细胞中存活率提高。这些结果与我们的临床数据一致,表明与对照组相比,MG 治疗可将 SARS-CoV2 感染患者的病毒载量减少 3.3 天,并减少对补充氧气的需求。我们希望我们的结果可以指导将 MG 定位为 COVID-19 患者的治疗选择的努力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec92/9159967/4780bd9a2d06/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec92/9159967/ae53fe9fabb6/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec92/9159967/385438a22a05/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec92/9159967/4780bd9a2d06/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec92/9159967/ae53fe9fabb6/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec92/9159967/385438a22a05/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec92/9159967/4780bd9a2d06/gr3_lrg.jpg

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