Robust antiviral activity of commonly prescribed antidepressants against emerging coronaviruses: in vitro and in silico drug repurposing studies
During the current coronavirus disease 2019 (COVID-19) pandemic, symptoms of depression are commonly documented among both symptomatic and asymptomatic quarantined COVID-19 patients. Despite that many of the FDA-approved drugs have been showed anti-SARS-CoV-2 activity in vitro and remarkable efficac...
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Published in | Scientific reports Vol. 12; no. 1; pp. 12920 - 12 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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London
Nature Publishing Group UK
28.07.2022
Nature Publishing Group Nature Portfolio |
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Abstract | During the current coronavirus disease 2019 (COVID-19) pandemic, symptoms of depression are commonly documented among both symptomatic and asymptomatic quarantined COVID-19 patients. Despite that many of the FDA-approved drugs have been showed anti-SARS-CoV-2 activity in vitro and remarkable efficacy against COVID-19 in clinical trials, no pharmaceutical products have yet been declared to be fully effective for treating COVID-19. Antidepressants comprise five major drug classes for the treatment of depression, neuralgia, migraine prophylaxis, and eating disorders which are frequently reported symptoms in COVID-19 patients. Herein, the efficacy of eight frequently prescribed FDA-approved antidepressants on the inhibition of both SARS-CoV-2 and MERS-CoV was assessed. Additionally, the in vitro anti-SARS-CoV-2 and anti-MERS-CoV activities were evaluated. Furthermore, molecular docking studies have been performed for these drugs against the spike (S) and main protease (M
pro
) pockets of both SARS-CoV-2 and MERS-CoV. Results showed that Amitriptyline, Imipramine, Paroxetine, and Sertraline had potential anti-viral activities. Our findings suggested that the aforementioned drugs deserve more in vitro and in vivo studies targeting COVID-19 especially for those patients suffering from depression. |
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AbstractList | During the current coronavirus disease 2019 (COVID-19) pandemic, symptoms of depression are commonly documented among both symptomatic and asymptomatic quarantined COVID-19 patients. Despite that many of the FDA-approved drugs have been showed anti-SARS-CoV-2 activity in vitro and remarkable efficacy against COVID-19 in clinical trials, no pharmaceutical products have yet been declared to be fully effective for treating COVID-19. Antidepressants comprise five major drug classes for the treatment of depression, neuralgia, migraine prophylaxis, and eating disorders which are frequently reported symptoms in COVID-19 patients. Herein, the efficacy of eight frequently prescribed FDA-approved antidepressants on the inhibition of both SARS-CoV-2 and MERS-CoV was assessed. Additionally, the in vitro anti-SARS-CoV-2 and anti-MERS-CoV activities were evaluated. Furthermore, molecular docking studies have been performed for these drugs against the spike (S) and main protease (M
pro
) pockets of both SARS-CoV-2 and MERS-CoV. Results showed that Amitriptyline, Imipramine, Paroxetine, and Sertraline had potential anti-viral activities. Our findings suggested that the aforementioned drugs deserve more in vitro and in vivo studies targeting COVID-19 especially for those patients suffering from depression. During the current coronavirus disease 2019 (COVID-19) pandemic, symptoms of depression are commonly documented among both symptomatic and asymptomatic quarantined COVID-19 patients. Despite that many of the FDA-approved drugs have been showed anti-SARS-CoV-2 activity in vitro and remarkable efficacy against COVID-19 in clinical trials, no pharmaceutical products have yet been declared to be fully effective for treating COVID-19. Antidepressants comprise five major drug classes for the treatment of depression, neuralgia, migraine prophylaxis, and eating disorders which are frequently reported symptoms in COVID-19 patients. Herein, the efficacy of eight frequently prescribed FDA-approved antidepressants on the inhibition of both SARS-CoV-2 and MERS-CoV was assessed. Additionally, the in vitro anti-SARS-CoV-2 and anti-MERS-CoV activities were evaluated. Furthermore, molecular docking studies have been performed for these drugs against the spike (S) and main protease (Mpro) pockets of both SARS-CoV-2 and MERS-CoV. Results showed that Amitriptyline, Imipramine, Paroxetine, and Sertraline had potential anti-viral activities. Our findings suggested that the aforementioned drugs deserve more in vitro and in vivo studies targeting COVID-19 especially for those patients suffering from depression. Abstract During the current coronavirus disease 2019 (COVID-19) pandemic, symptoms of depression are commonly documented among both symptomatic and asymptomatic quarantined COVID-19 patients. Despite that many of the FDA-approved drugs have been showed anti-SARS-CoV-2 activity in vitro and remarkable efficacy against COVID-19 in clinical trials, no pharmaceutical products have yet been declared to be fully effective for treating COVID-19. Antidepressants comprise five major drug classes for the treatment of depression, neuralgia, migraine prophylaxis, and eating disorders which are frequently reported symptoms in COVID-19 patients. Herein, the efficacy of eight frequently prescribed FDA-approved antidepressants on the inhibition of both SARS-CoV-2 and MERS-CoV was assessed. Additionally, the in vitro anti-SARS-CoV-2 and anti-MERS-CoV activities were evaluated. Furthermore, molecular docking studies have been performed for these drugs against the spike (S) and main protease (Mpro) pockets of both SARS-CoV-2 and MERS-CoV. Results showed that Amitriptyline, Imipramine, Paroxetine, and Sertraline had potential anti-viral activities. Our findings suggested that the aforementioned drugs deserve more in vitro and in vivo studies targeting COVID-19 especially for those patients suffering from depression. During the current coronavirus disease 2019 (COVID-19) pandemic, symptoms of depression are commonly documented among both symptomatic and asymptomatic quarantined COVID-19 patients. Despite that many of the FDA-approved drugs have been showed anti-SARS-CoV-2 activity in vitro and remarkable efficacy against COVID-19 in clinical trials, no pharmaceutical products have yet been declared to be fully effective for treating COVID-19. Antidepressants comprise five major drug classes for the treatment of depression, neuralgia, migraine prophylaxis, and eating disorders which are frequently reported symptoms in COVID-19 patients. Herein, the efficacy of eight frequently prescribed FDA-approved antidepressants on the inhibition of both SARS-CoV-2 and MERS-CoV was assessed. Additionally, the in vitro anti-SARS-CoV-2 and anti-MERS-CoV activities were evaluated. Furthermore, molecular docking studies have been performed for these drugs against the spike (S) and main protease (Mpro) pockets of both SARS-CoV-2 and MERS-CoV. Results showed that Amitriptyline, Imipramine, Paroxetine, and Sertraline had potential anti-viral activities. Our findings suggested that the aforementioned drugs deserve more in vitro and in vivo studies targeting COVID-19 especially for those patients suffering from depression.During the current coronavirus disease 2019 (COVID-19) pandemic, symptoms of depression are commonly documented among both symptomatic and asymptomatic quarantined COVID-19 patients. Despite that many of the FDA-approved drugs have been showed anti-SARS-CoV-2 activity in vitro and remarkable efficacy against COVID-19 in clinical trials, no pharmaceutical products have yet been declared to be fully effective for treating COVID-19. Antidepressants comprise five major drug classes for the treatment of depression, neuralgia, migraine prophylaxis, and eating disorders which are frequently reported symptoms in COVID-19 patients. Herein, the efficacy of eight frequently prescribed FDA-approved antidepressants on the inhibition of both SARS-CoV-2 and MERS-CoV was assessed. Additionally, the in vitro anti-SARS-CoV-2 and anti-MERS-CoV activities were evaluated. Furthermore, molecular docking studies have been performed for these drugs against the spike (S) and main protease (Mpro) pockets of both SARS-CoV-2 and MERS-CoV. Results showed that Amitriptyline, Imipramine, Paroxetine, and Sertraline had potential anti-viral activities. Our findings suggested that the aforementioned drugs deserve more in vitro and in vivo studies targeting COVID-19 especially for those patients suffering from depression. |
ArticleNumber | 12920 |
Author | Mahmoud, Dina B. Al‐Karmalawy, Ahmed A. Abo Shama, Noura M. Abulkhair, Hamada S. Moatasim, Yassmin Gomaa, Mokhtar R. Kandeil, Ahmed Ali, Mohamed A. Kutkat, Omnia Mostafa, Ahmed El-Taweel, Ahmed N. GabAllah, Mohamed Kayali, Ghazi |
Author_xml | – sequence: 1 givenname: Omnia surname: Kutkat fullname: Kutkat, Omnia organization: Center of Scientific Excellence for Influenza Viruses, National Research Centre – sequence: 2 givenname: Yassmin surname: Moatasim fullname: Moatasim, Yassmin organization: Center of Scientific Excellence for Influenza Viruses, National Research Centre – sequence: 3 givenname: Ahmed A. surname: Al‐Karmalawy fullname: Al‐Karmalawy, Ahmed A. organization: Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Horus University-Egypt – sequence: 4 givenname: Hamada S. surname: Abulkhair fullname: Abulkhair, Hamada S. organization: Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Horus University-Egypt, Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Al-Azhar University – sequence: 5 givenname: Mokhtar R. surname: Gomaa fullname: Gomaa, Mokhtar R. organization: Center of Scientific Excellence for Influenza Viruses, National Research Centre – sequence: 6 givenname: Ahmed N. surname: El-Taweel fullname: El-Taweel, Ahmed N. organization: Center of Scientific Excellence for Influenza Viruses, National Research Centre – sequence: 7 givenname: Noura M. surname: Abo Shama fullname: Abo Shama, Noura M. organization: Center of Scientific Excellence for Influenza Viruses, National Research Centre – sequence: 8 givenname: Mohamed surname: GabAllah fullname: GabAllah, Mohamed organization: Center of Scientific Excellence for Influenza Viruses, National Research Centre – sequence: 9 givenname: Dina B. surname: Mahmoud fullname: Mahmoud, Dina B. organization: Pharmaceutics Department, Egyptian Drug Authority, formerly known as National Organization for Drug Control and Research – sequence: 10 givenname: Ghazi surname: Kayali fullname: Kayali, Ghazi organization: Department of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas, Human Link DMCC – sequence: 11 givenname: Mohamed A. surname: Ali fullname: Ali, Mohamed A. organization: Center of Scientific Excellence for Influenza Viruses, National Research Centre – sequence: 12 givenname: Ahmed surname: Kandeil fullname: Kandeil, Ahmed email: kandeil_a@hotmail.com organization: Center of Scientific Excellence for Influenza Viruses, National Research Centre – sequence: 13 givenname: Ahmed surname: Mostafa fullname: Mostafa, Ahmed email: ahmed_elsayed@daad-alumni.de organization: Center of Scientific Excellence for Influenza Viruses, National Research Centre |
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SubjectTerms | 631/154 639/638 692/699 Amitriptyline Antidepressants Antiviral activity Antiviral agents Antiviral drugs Clinical trials Coronaviruses COVID-19 Eating disorders Headache Humanities and Social Sciences Imipramine Mental depression Middle East respiratory syndrome Migraine multidisciplinary Neuralgia Pandemics Paroxetine Patients Prophylaxis Science Science (multidisciplinary) Sertraline Severe acute respiratory syndrome coronavirus 2 |
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Title | Robust antiviral activity of commonly prescribed antidepressants against emerging coronaviruses: in vitro and in silico drug repurposing studies |
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