Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Nov;13(6):1048-1054.
doi: 10.1111/cts.12862. Epub 2020 Aug 29.

Effect of Common Medications on the Expression of SARS-CoV-2 Entry Receptors in Kidney Tissue

Affiliations

Effect of Common Medications on the Expression of SARS-CoV-2 Entry Receptors in Kidney Tissue

Narjes Saheb Sharif-Askari et al. Clin Transl Sci. 2020 Nov.

Abstract

Besides the respiratory system, severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) infection was shown to affect other essential organs such as the kidneys. Early kidney involvement during the course of infection was associated with worse outcomes, which could be attributed to the direct SARS-CoV-2 infection of kidney cells. In this study, the effect of commonly used medications on the expression of SARS-CoV-2 receptor, angiotensin-converting enzyme (ACE)2, and TMPRSS2 protein in kidney tissues was evaluated. This was done by in silico analyses of publicly available transcriptomic databases of kidney tissues of rats treated with multiple doses of commonly used medications. Of 59 tested medications, 56% modified ACE2 expression, whereas 24% modified TMPRSS2 expression. ACE2 was increased with only a few of the tested medication groups, namely the renin-angiotensin inhibitors, such as enalapril, antibacterial agents, such as nitrofurantoin, and the proton pump inhibitor, omeprazole. The majority of the other medications decreased ACE2 expression to variable degrees with allopurinol and cisplatin causing the most noticeable downregulation. The expression level of TMPRSS2 was increased with a number of medications, such as diclofenac, furosemide, and dexamethasone, whereas other medications, such as allopurinol, suppressed the expression of this gene. The prolonged exposure to combinations of these medications could regulate the expression of ACE2 and TMPRSS2 in a way that may affect kidney susceptibility to SARS-CoV-2 infection. Data presented here suggest that we should be vigilant about the potential effects of commonly used medications on kidney tissue expression of ACE2 and TMPRSS2.

PubMed Disclaimer

Conflict of interest statement

The authors declared no competing interests for this work.

Figures

Figure 1
Figure 1
Effect of common medications on the expression levels of severe acute respiratory syndrome‐coronavirus 2 entry receptors in kidney. (a) Shows the baseline expression of angiotensin‐converting enzyme (ACE)2 and TMPRSS2 in healthy lung and kidney tissues extracted from the Genotype‐Tissue Expression project. (b) Represents the main medication classes that affected the expression levels of ACE2. (c–e) Shows medications causing the highest and lowest fold change for ACE2 TMPRSS2, and CD147 expression levels.

References

    1. Xiao, F. et al Evidence for gastrointestinal infection of SARS‐CoV‐2. Gastroenterology 158, 1831–1833.e1833 (2020). - PMC - PubMed
    1. Huang, C. et al Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 395, 497–506 (2020). - PMC - PubMed
    1. Cheng, Y. et al Kidney disease is associated with in‐hospital death of patients with COVID‐19. Kidney Int. 97, 829–838 (2020). - PMC - PubMed
    1. Ronco, C. , Reis, T. & Husain‐Syed, F. Management of acute kidney injury in patients with COVID‐19. Lancet Resp Med. 8, 738–742 (2020). - PMC - PubMed
    1. Peiris, J.S. et al Clinical progression and viral load in a community outbreak of coronavirus‐associated SARS pneumonia: a prospective study. Lancet 361, 1767–1772 (2003). - PMC - PubMed

Publication types

LinkOut - more resources