Cargando…
Astemizole as a drug to inhibit the effect of SARS-COV-2 in vitro
Since the beginning of December 2019, a novel Coronavirus severe respiratory disease, caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) which also been termed 2019-new CoV (2019-nCoV), has continued to spread worldwide. As of August 27, 2020, a total of 24,232,429 people have be...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ltd.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8081582/ https://www.ncbi.nlm.nih.gov/pubmed/33932547 http://dx.doi.org/10.1016/j.micpath.2021.104929 |
_version_ | 1783685672187461632 |
---|---|
author | Wang, Xiangjun Lu, Jiayu Ge, Shuai Hou, Yajing Hu, Tian Lv, Yuexin Wang, Cheng He, Huaizhen |
author_facet | Wang, Xiangjun Lu, Jiayu Ge, Shuai Hou, Yajing Hu, Tian Lv, Yuexin Wang, Cheng He, Huaizhen |
author_sort | Wang, Xiangjun |
collection | PubMed |
description | Since the beginning of December 2019, a novel Coronavirus severe respiratory disease, caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) which also been termed 2019-new CoV (2019-nCoV), has continued to spread worldwide. As of August 27, 2020, a total of 24,232,429 people have been infected and 826,518 people have died. In our study, we found that astemizole can antagonize ACE2 and inhibit the entry of SARS-COV-2 spike pseudovirus into ACE2-expressed HEK293T cells (ACE2hi cells). We analysied the binding character of astemizole to ACE2 by molecular docking and surface plasmon resonance (SPR) assays and molecule docking, SARS-COV-2 spike pseudotype virus was also taken to investigate the suppression viropexis effect of astemizole. The results showed that astemizole can bind to the ACE2 receptor and inhibit the invasion of SARS-COV-2 Spike pseudoviruses. Thus astemizole represent potential drug candidates that can be re-used in anti-coronavirus therapies. |
format | Online Article Text |
id | pubmed-8081582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80815822021-04-29 Astemizole as a drug to inhibit the effect of SARS-COV-2 in vitro Wang, Xiangjun Lu, Jiayu Ge, Shuai Hou, Yajing Hu, Tian Lv, Yuexin Wang, Cheng He, Huaizhen Microb Pathog Article Since the beginning of December 2019, a novel Coronavirus severe respiratory disease, caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) which also been termed 2019-new CoV (2019-nCoV), has continued to spread worldwide. As of August 27, 2020, a total of 24,232,429 people have been infected and 826,518 people have died. In our study, we found that astemizole can antagonize ACE2 and inhibit the entry of SARS-COV-2 spike pseudovirus into ACE2-expressed HEK293T cells (ACE2hi cells). We analysied the binding character of astemizole to ACE2 by molecular docking and surface plasmon resonance (SPR) assays and molecule docking, SARS-COV-2 spike pseudotype virus was also taken to investigate the suppression viropexis effect of astemizole. The results showed that astemizole can bind to the ACE2 receptor and inhibit the invasion of SARS-COV-2 Spike pseudoviruses. Thus astemizole represent potential drug candidates that can be re-used in anti-coronavirus therapies. Published by Elsevier Ltd. 2021-07 2021-04-29 /pmc/articles/PMC8081582/ /pubmed/33932547 http://dx.doi.org/10.1016/j.micpath.2021.104929 Text en © 2021 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Wang, Xiangjun Lu, Jiayu Ge, Shuai Hou, Yajing Hu, Tian Lv, Yuexin Wang, Cheng He, Huaizhen Astemizole as a drug to inhibit the effect of SARS-COV-2 in vitro |
title | Astemizole as a drug to inhibit the effect of SARS-COV-2 in vitro |
title_full | Astemizole as a drug to inhibit the effect of SARS-COV-2 in vitro |
title_fullStr | Astemizole as a drug to inhibit the effect of SARS-COV-2 in vitro |
title_full_unstemmed | Astemizole as a drug to inhibit the effect of SARS-COV-2 in vitro |
title_short | Astemizole as a drug to inhibit the effect of SARS-COV-2 in vitro |
title_sort | astemizole as a drug to inhibit the effect of sars-cov-2 in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8081582/ https://www.ncbi.nlm.nih.gov/pubmed/33932547 http://dx.doi.org/10.1016/j.micpath.2021.104929 |
work_keys_str_mv | AT wangxiangjun astemizoleasadrugtoinhibittheeffectofsarscov2invitro AT lujiayu astemizoleasadrugtoinhibittheeffectofsarscov2invitro AT geshuai astemizoleasadrugtoinhibittheeffectofsarscov2invitro AT houyajing astemizoleasadrugtoinhibittheeffectofsarscov2invitro AT hutian astemizoleasadrugtoinhibittheeffectofsarscov2invitro AT lvyuexin astemizoleasadrugtoinhibittheeffectofsarscov2invitro AT wangcheng astemizoleasadrugtoinhibittheeffectofsarscov2invitro AT hehuaizhen astemizoleasadrugtoinhibittheeffectofsarscov2invitro |