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COVID-19治疗中地塞米松血管转运的分子决定因素。

Molecular determinants of vascular transport of dexamethasone in COVID-19 therapy.

作者信息

Shabalin Ivan G, Czub Mateusz P, Majorek Karolina A, Brzezinski Dariusz, Grabowski Marek, Cooper David R, Panasiuk Mateusz, Chruszcz Maksymilian, Minor Wladek

机构信息

Department of Molecular Physiology and Biological Physics, University of Virginia, 1340 Jefferson Park Avenue, Charlottesville, VA 22908, USA.

Center for Biocrystallographic Research, Institute of Bioorganic Chemistry, Polish Academy of Sciences, 61-704 Poznan, Poland.

出版信息

IUCrJ. 2020 Sep 29;7(Pt 6):1048-58. doi: 10.1107/S2052252520012944.

Abstract

Dexamethasone, a widely used corticosteroid, has recently been reported as the first drug to increase the survival chances of patients with severe COVID-19. Therapeutic agents, including dexamethasone, are mostly transported through the body by binding to serum albumin. Here, the first structure of serum albumin in complex with dexamethasone is reported. Dexamethasone binds to drug site 7, which is also the binding site for commonly used nonsteroidal anti-inflammatory drugs and testosterone, suggesting potentially problematic binding competition. This study bridges structural findings with an analysis of publicly available clinical data from Wuhan and suggests that an adjustment of the dexamethasone regimen should be further investigated as a strategy for patients affected by two major COVID-19 risk factors: low albumin levels and diabetes.

摘要

地塞米松是一种广泛使用的皮质类固醇,最近有报道称它是第一种能提高重症 COVID-19 患者生存几率的药物。包括地塞米松在内的治疗药物大多通过与血清白蛋白结合在体内运输。在此,报道了血清白蛋白与地塞米松复合物的首个结构。地塞米松与药物结合位点 7 结合,该位点也是常用非甾体抗炎药和睾酮的结合位点,这表明可能存在有问题的结合竞争。这项研究将结构研究结果与对来自武汉的公开临床数据的分析相结合,并表明作为一种针对受两个主要 COVID-19 风险因素影响的患者的策略,即低白蛋白水平和糖尿病,应进一步研究调整地塞米松治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b5c/7642781/bd2444986cd3/m-07-01048-fig1.jpg

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