Gazi University, Faculty of Pharmacy, Department of Toxicology, Ankara, Turkey.
Ankara University, Biotechnology Institute, Gumusdere Campus, Kecioren, Ankara, Turkey.
Environ Toxicol Pharmacol. 2020 Oct;79:103436. doi: 10.1016/j.etap.2020.103436. Epub 2020 Jun 17.
Recent analysis concerning the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)- angiotensin converting enzyme (ACE) receptor interaction in enterocytes, the definition of gut-lung axis, as well as the molecular basis of sialic acid-related dual recognition concept in gastrointestinal SARS-CoV-2 infection, have brought a new perspective to potential therapeutic targets. In this review evolving research and clinical data on gastrointestinal SARS-CoV-2 infection are discussed in the context of viral fusion and entry mechanisms, focusing on the different triggers used by coronaviruses. Furthermore, it is emphasized that the viral spike protein is prevented from binding gangliosides, which are composed of a glycosphingolipid with one or more sialic acids, in the presence of chloroquine or hydroxychloroquine. In gastrointestinal SARS-CoV-2 infection the efficiency of these repositioned drugs is debated.
最近对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)与肠细胞中的血管紧张素转换酶(ACE)受体相互作用、肠道-肺轴的定义以及胃肠道 SARS-CoV-2 感染中与唾液酸相关的双重识别概念的分子基础的分析,为潜在的治疗靶点带来了新的视角。在这篇综述中,讨论了胃肠道 SARS-CoV-2 感染的不断发展的研究和临床数据,重点介绍了冠状病毒使用的不同触发因素。此外,还强调了在氯喹或羟氯喹存在的情况下,病毒的刺突蛋白可防止与神经节苷脂结合,神经节苷脂是由含有一个或多个唾液酸的糖脂组成的。在胃肠道 SARS-CoV-2 感染中,这些重新定位药物的效果存在争议。