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Niclosamide for Covid-19: bridging the gap

AIM/PURPOSE: Niclosamide (NCL) is an anthelminthic drug, which is widely used to treat various diseases due to its pleiotropic anti-inflammatory and antiviral activities. NCL modulates of uncoupling oxidative phosphorylation and different signaling pathways in human biological processes. The wide-sp...

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Autores principales: Al-kuraishy, Hayder M., Al-Gareeb, Ali I., Alzahrani, Khalid J., Alexiou, Athanasios, Batiha, Gaber El-Saber
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522539/
https://www.ncbi.nlm.nih.gov/pubmed/34664162
http://dx.doi.org/10.1007/s11033-021-06770-7
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author Al-kuraishy, Hayder M.
Al-Gareeb, Ali I.
Alzahrani, Khalid J.
Alexiou, Athanasios
Batiha, Gaber El-Saber
author_facet Al-kuraishy, Hayder M.
Al-Gareeb, Ali I.
Alzahrani, Khalid J.
Alexiou, Athanasios
Batiha, Gaber El-Saber
author_sort Al-kuraishy, Hayder M.
collection PubMed
description AIM/PURPOSE: Niclosamide (NCL) is an anthelminthic drug, which is widely used to treat various diseases due to its pleiotropic anti-inflammatory and antiviral activities. NCL modulates of uncoupling oxidative phosphorylation and different signaling pathways in human biological processes. The wide-spectrum antiviral effect of NCL makes it a possible candidate for recent pandemic SARS-CoV-2 infection and may reduce Covid-19 severity. Therefore, the aim of the present study was to review and clarify the potential role of NCL in Covid-19. METHODS: This study reviewed and highlighted the protective role of NCL therapy in Covid-19. A related literature search in PubMed, Scopus, Web of Science, Google Scholar, and Science Direct was done. RESULTS: NCL has noteworthy anti-inflammatory and antiviral effects. The primary antiviral mechanism of NCL is through neutralization of endosomal PH and inhibition of viral protein maturation. NCL acts as a proton carrier, inhibits homeostasis of endosomal PH, which limiting of viral proliferation and release. The anti-inflammatory effects of NCL are mediated by suppression of inflammatory signaling pathways and release of pro-inflammatory cytokines. However, the major limitation in using NCL is low aqueous solubility, which reduces oral bioavailability and therapeutic serum concentration that reducing the in vivo effect of NCL against SARS-CoV-2. CONCLUSIONS: NCL has anti-inflammatory and immune regulatory effects by modulating the release of pro-inflammatory cytokines, inhibition of NF-κB /NLRP3 inflammasome and mTOR signaling pathway. NCL has an anti-SARS-CoV-2 effect via interruption of viral life-cycle and/or induction of cytopathic effect. Prospective clinical studies and clinical trials are mandatory to confirm the potential role of NCL in patients with Covid-19 concerning the severity and clinical outcomes.
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spelling pubmed-85225392021-10-20 Niclosamide for Covid-19: bridging the gap Al-kuraishy, Hayder M. Al-Gareeb, Ali I. Alzahrani, Khalid J. Alexiou, Athanasios Batiha, Gaber El-Saber Mol Biol Rep Mini Review Article AIM/PURPOSE: Niclosamide (NCL) is an anthelminthic drug, which is widely used to treat various diseases due to its pleiotropic anti-inflammatory and antiviral activities. NCL modulates of uncoupling oxidative phosphorylation and different signaling pathways in human biological processes. The wide-spectrum antiviral effect of NCL makes it a possible candidate for recent pandemic SARS-CoV-2 infection and may reduce Covid-19 severity. Therefore, the aim of the present study was to review and clarify the potential role of NCL in Covid-19. METHODS: This study reviewed and highlighted the protective role of NCL therapy in Covid-19. A related literature search in PubMed, Scopus, Web of Science, Google Scholar, and Science Direct was done. RESULTS: NCL has noteworthy anti-inflammatory and antiviral effects. The primary antiviral mechanism of NCL is through neutralization of endosomal PH and inhibition of viral protein maturation. NCL acts as a proton carrier, inhibits homeostasis of endosomal PH, which limiting of viral proliferation and release. The anti-inflammatory effects of NCL are mediated by suppression of inflammatory signaling pathways and release of pro-inflammatory cytokines. However, the major limitation in using NCL is low aqueous solubility, which reduces oral bioavailability and therapeutic serum concentration that reducing the in vivo effect of NCL against SARS-CoV-2. CONCLUSIONS: NCL has anti-inflammatory and immune regulatory effects by modulating the release of pro-inflammatory cytokines, inhibition of NF-κB /NLRP3 inflammasome and mTOR signaling pathway. NCL has an anti-SARS-CoV-2 effect via interruption of viral life-cycle and/or induction of cytopathic effect. Prospective clinical studies and clinical trials are mandatory to confirm the potential role of NCL in patients with Covid-19 concerning the severity and clinical outcomes. Springer Netherlands 2021-10-18 2021 /pmc/articles/PMC8522539/ /pubmed/34664162 http://dx.doi.org/10.1007/s11033-021-06770-7 Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Mini Review Article
Al-kuraishy, Hayder M.
Al-Gareeb, Ali I.
Alzahrani, Khalid J.
Alexiou, Athanasios
Batiha, Gaber El-Saber
Niclosamide for Covid-19: bridging the gap
title Niclosamide for Covid-19: bridging the gap
title_full Niclosamide for Covid-19: bridging the gap
title_fullStr Niclosamide for Covid-19: bridging the gap
title_full_unstemmed Niclosamide for Covid-19: bridging the gap
title_short Niclosamide for Covid-19: bridging the gap
title_sort niclosamide for covid-19: bridging the gap
topic Mini Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522539/
https://www.ncbi.nlm.nih.gov/pubmed/34664162
http://dx.doi.org/10.1007/s11033-021-06770-7
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