Cargando…

Drug repurposing of anti-infective clinical drugs: Discovery of two potential anti-cytokine storm agents

Coronavirus Disease 2019 (COVID-19) caused by Severe Acute Respiratory Syndrome Coronavirus -2 (SARS-CoV-2) has been widely spread in the world with a high mortality. Cytokine storm syndrome (CSS) and acute lung injury caused by SARS-CoV-2 infection severely threaten the patients. With the purpose t...

Descripción completa

Detalles Bibliográficos
Autores principales: Su, Li, Tu, Ye, Kong, De-pei, Chen, Da-gui, Zhang, Chen-xi, Zhang, Wan-nian, Zhuang, Chun-lin, Wang, Zhi-bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Author(s). Published by Elsevier Masson SAS. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443334/
https://www.ncbi.nlm.nih.gov/pubmed/32846329
http://dx.doi.org/10.1016/j.biopha.2020.110643
_version_ 1783573614703935488
author Su, Li
Tu, Ye
Kong, De-pei
Chen, Da-gui
Zhang, Chen-xi
Zhang, Wan-nian
Zhuang, Chun-lin
Wang, Zhi-bin
author_facet Su, Li
Tu, Ye
Kong, De-pei
Chen, Da-gui
Zhang, Chen-xi
Zhang, Wan-nian
Zhuang, Chun-lin
Wang, Zhi-bin
author_sort Su, Li
collection PubMed
description Coronavirus Disease 2019 (COVID-19) caused by Severe Acute Respiratory Syndrome Coronavirus -2 (SARS-CoV-2) has been widely spread in the world with a high mortality. Cytokine storm syndrome (CSS) and acute lung injury caused by SARS-CoV-2 infection severely threaten the patients. With the purpose to find effective and low-toxic drugs to mitigate CSS, entecavir and imipenem were identified to reduce TNF-α using a LPS-induced macrophage model from the anti-infective drug library. Entecavir and imipenem efficiently suppressed the release of inflammatory cytokines by partly intervention of NF-κB activity. The acute lung injury was also alleviated and the survival time was prolonged in mice. In addition, entecavir and imipenem inhibited the release of TNF-α and IL-10 in human peripheral blood mononuclear cells (hPBMCs). Collectively, we proposed that entecavir and imipenem might be candidates for the treatment of CSS.
format Online
Article
Text
id pubmed-7443334
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The Author(s). Published by Elsevier Masson SAS.
record_format MEDLINE/PubMed
spelling pubmed-74433342020-08-24 Drug repurposing of anti-infective clinical drugs: Discovery of two potential anti-cytokine storm agents Su, Li Tu, Ye Kong, De-pei Chen, Da-gui Zhang, Chen-xi Zhang, Wan-nian Zhuang, Chun-lin Wang, Zhi-bin Biomed Pharmacother Short Communication Coronavirus Disease 2019 (COVID-19) caused by Severe Acute Respiratory Syndrome Coronavirus -2 (SARS-CoV-2) has been widely spread in the world with a high mortality. Cytokine storm syndrome (CSS) and acute lung injury caused by SARS-CoV-2 infection severely threaten the patients. With the purpose to find effective and low-toxic drugs to mitigate CSS, entecavir and imipenem were identified to reduce TNF-α using a LPS-induced macrophage model from the anti-infective drug library. Entecavir and imipenem efficiently suppressed the release of inflammatory cytokines by partly intervention of NF-κB activity. The acute lung injury was also alleviated and the survival time was prolonged in mice. In addition, entecavir and imipenem inhibited the release of TNF-α and IL-10 in human peripheral blood mononuclear cells (hPBMCs). Collectively, we proposed that entecavir and imipenem might be candidates for the treatment of CSS. The Author(s). Published by Elsevier Masson SAS. 2020-11 2020-08-23 /pmc/articles/PMC7443334/ /pubmed/32846329 http://dx.doi.org/10.1016/j.biopha.2020.110643 Text en © 2020 The Author(s) 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 Short Communication
Su, Li
Tu, Ye
Kong, De-pei
Chen, Da-gui
Zhang, Chen-xi
Zhang, Wan-nian
Zhuang, Chun-lin
Wang, Zhi-bin
Drug repurposing of anti-infective clinical drugs: Discovery of two potential anti-cytokine storm agents
title Drug repurposing of anti-infective clinical drugs: Discovery of two potential anti-cytokine storm agents
title_full Drug repurposing of anti-infective clinical drugs: Discovery of two potential anti-cytokine storm agents
title_fullStr Drug repurposing of anti-infective clinical drugs: Discovery of two potential anti-cytokine storm agents
title_full_unstemmed Drug repurposing of anti-infective clinical drugs: Discovery of two potential anti-cytokine storm agents
title_short Drug repurposing of anti-infective clinical drugs: Discovery of two potential anti-cytokine storm agents
title_sort drug repurposing of anti-infective clinical drugs: discovery of two potential anti-cytokine storm agents
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443334/
https://www.ncbi.nlm.nih.gov/pubmed/32846329
http://dx.doi.org/10.1016/j.biopha.2020.110643
work_keys_str_mv AT suli drugrepurposingofantiinfectiveclinicaldrugsdiscoveryoftwopotentialanticytokinestormagents
AT tuye drugrepurposingofantiinfectiveclinicaldrugsdiscoveryoftwopotentialanticytokinestormagents
AT kongdepei drugrepurposingofantiinfectiveclinicaldrugsdiscoveryoftwopotentialanticytokinestormagents
AT chendagui drugrepurposingofantiinfectiveclinicaldrugsdiscoveryoftwopotentialanticytokinestormagents
AT zhangchenxi drugrepurposingofantiinfectiveclinicaldrugsdiscoveryoftwopotentialanticytokinestormagents
AT zhangwannian drugrepurposingofantiinfectiveclinicaldrugsdiscoveryoftwopotentialanticytokinestormagents
AT zhuangchunlin drugrepurposingofantiinfectiveclinicaldrugsdiscoveryoftwopotentialanticytokinestormagents
AT wangzhibin drugrepurposingofantiinfectiveclinicaldrugsdiscoveryoftwopotentialanticytokinestormagents