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Angiotensin converting enzyme-2 as therapeutic target in COVID-19
Neda Roshanravan1, Samad Ghaffari1, Mehdi Hedayati2
1Cardiovascular Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Abstract:
The pandemic of coronavirus disease 2019 (COVID-19) is a global health emergency that poses a significant threat to world people's health. This outbreak causes major challenges to healthcare systems. Given the lack of effective treatments or vaccine for it, the identification of novel and safe drugs against COVID-19 infection is an urgent need. Angiotensin-converting enzyme 2 (ACE2) is not only an entry receptor of the SARS-CoV-2 virus, the virus that causes COVID-19, but also can protect from lung injury. In this view, we highlighted potential approaches to address ACE2-mediated SARS-CoV-2 virus, including 1) delivering an excessive soluble form of ACE2 (recombinant human ACE2: rhACE2) and 2) inhibition of the interaction between SARS-CoV-2 virus and ACE2 by some compounds with competitive effects (morphine and codeine). Further clinical trials in this regard can reveal a more definite conclusion against the COVID-19 disaster.
Insights
Researchers explored strategies to combat COVID-19 by targeting the ACE2 receptor. Potential treatments include using soluble ACE2 and compounds like morphine to block viral entry, offering hope against the pandemic.
Area of Science:
- Virology
- Infectious Diseases
- Pharmacology
Background:
- The COVID-19 pandemic presents a severe global health crisis, straining healthcare systems worldwide.
- Effective treatments and vaccines for COVID-19 are currently lacking, necessitating urgent development of novel therapeutic strategies.
- Angiotensin-converting enzyme 2 (ACE2) plays a dual role as the entry receptor for SARS-CoV-2 and a protective factor against lung injury.
Purpose of the Study:
- To identify and highlight potential therapeutic approaches targeting the ACE2 receptor for combating SARS-CoV-2 infection.
- To explore strategies that modulate the interaction between SARS-CoV-2 and ACE2 to mitigate viral pathogenesis.
Main Methods:
- Investigated the delivery of a soluble form of ACE2 (recombinant human ACE2: rhACE2) to intercept the virus.
- Examined the potential of compounds like morphine and codeine to inhibit the interaction between SARS-CoV-2 and ACE2 through competitive binding.
Main Results:
- The study proposes two primary strategies for therapeutic intervention against SARS-CoV-2 via ACE2 modulation.
- Recombinant human ACE2 (rhACE2) offers a potential method to sequester the virus.
- Morphine and codeine are identified as potential inhibitors of the virus-ACE2 interaction.
Conclusions:
- Targeting the ACE2 receptor presents a promising avenue for developing novel COVID-19 therapies.
- Further clinical investigations are crucial to validate the efficacy and safety of rhACE2 and competitive inhibitors like morphine and codeine.
- These approaches could offer a significant contribution to managing the ongoing COVID-19 pandemic.
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