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血管紧张素转换酶2和跨膜丝氨酸蛋白酶2的潜在双重抑制剂

Potential Simultaneous Inhibitors of Angiotensin-Converting Enzyme 2 and Transmembrane Protease, Serine 2.

作者信息

Wu Ching-Yuan, Lin Yu-Shih, Yang Yao-Hsu, Shu Li-Hsin, Cheng Yu-Ching, Liu Hung Te

机构信息

Department of Traditional Chinese Medicine, Chang Gung Memorial Hospital, Chiayi, Taiwan.

School of Chinese Medicine, College of Medicine, Chang Gung University, Chiayi, Taiwan.

出版信息

Front Pharmacol. 2020 Dec 17;11:584158. doi: 10.3389/fphar.2020.584158. eCollection 2020.

Abstract

Outbreak of coronavirus disease 2019 occurred in Wuhan and has rapidly spread to almost all parts of world. GB-1, the herbal formula from Tian Shang Sheng Mu of Chiayi Puzi Peitian Temple, is used for the prophylaxis of SARS-CoV-2 in Taiwan. In this study, we investigated that the effect of GB-1 and the index compounds of GB-1 on the ACE2 and TMPRSS2 expression through and study. In our result, GB-1 can inhibit ACE2 and TMPRSS2 protein expression in HepG2 cells, 293T cells, and Caco-2 cells without cytotoxicity. For the mouse model, GB-1 treatment could decrease ACE2 and TMPRSS2 expression levels of the lung and kidney tissue without adverse effects, including nephrotoxicity and hepatotoxicity. In the compositions of GB-1, 0.5-1 mg/ml of Fisch. ex DC extract could not inhibit mRNA and protein expression in HepG2 cells. In addition, theaflavin-3-gallate could inhibit protein expression of ACE2 and TMPRSS2 without significant cytotoxicity. Our results suggest that GB-1 and theaflavin-3-gallate could act as potential candidates for prophylaxis or treatment of SARS-CoV-2 infection through inhibiting protein expression of ACE2 and TMPRSS2 for the further study.

摘要

2019冠状病毒病疫情在武汉爆发,并迅速蔓延至全球几乎所有地区。嘉义朴子配天宫天上圣母的中药配方GB-1在台湾用于预防严重急性呼吸综合征冠状病毒2(SARS-CoV-2)。在本研究中,我们通过[具体研究方法]研究了GB-1及其指标性成分对血管紧张素转换酶2(ACE2)和跨膜丝氨酸蛋白酶2(TMPRSS2)表达的影响。结果显示,GB-1可抑制人肝癌细胞(HepG2细胞)、人胚肾细胞(293T细胞)和人结肠腺癌细胞(Caco-2细胞)中ACE2和TMPRSS2蛋白的表达,且无细胞毒性。对于小鼠模型,GB-1治疗可降低肺和肾组织中ACE2和TMPRSS2的表达水平,且无包括肾毒性和肝毒性在内的不良反应。在GB-1的成分中,0.5-1毫克/毫升的[具体植物名称] Fisch. ex DC提取物不能抑制HepG2细胞中[相关基因]的mRNA和蛋白表达。此外,茶黄素-3-没食子酸酯可抑制ACE2和TMPRSS2的蛋白表达,且无明显细胞毒性。我们的研究结果表明,GB-1和茶黄素-3-没食子酸酯可能通过抑制ACE2和TMPRSS2的蛋白表达,作为预防或治疗SARS-CoV-2感染的潜在候选药物,有待进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d52e/7773841/ced9b5d6cd50/fphar-11-584158-g001.jpg

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