Related Experiment Video
Updated: Jun 13, 2025

Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro
Published on: March 17, 2023
Perindopril decreases angiotensin-converting enzyme 2 (ACE2) expression in human adipocytes exposed to SARS-CoV-2 S1
Primasitha M Harsoyo1,2, Meity Ardiana1,2, Hanestya O Hermawan1,2
1Department of Cardiology and Vascular Medicine, Faculty of Medical, Universitas Airlangga, Surabaya, Indonesia.
Abstract:
The expression of angiotensin-converting enzyme 2 (ACE2) in the adipose tissues of obese patients needs further study, as it may aid infection and serve as a viral reservoir. There has been controversy over whether to use ACE inhibitors to prevent coronavirus disease 2019 (COVID-19) severity. Perindopril, an ACE2 inhibitor, has been proposed; however, its relationship with COVID-19 has not yet been clear. The aim of this study was to investigate the effect of perindopril to reduce the expression of ACE2 and pro-inflammatory cytokine in adipocytes exposed to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Enzymatic isolation of adipose tissues was performed from obese male donor patients aged 30-50 years, then exposed it with SARS-CoV-2 S1 spike protein. This study also included human recombinant ACE2 (hrsACE2) as a comparison to perindopril. The expression of ACE2 was evaluated using ELISA. Our data indicated that SARS-CoV-2 Spike protein exposure increased ACE2 expression significantly. Administration of perindopril decreased ACE2 expression (43.37 μg/mL) significantly compared to the positive group (80.31 μg/mL) (p<0.001). Perindopril administration also decreased IL-6 levels significantly compared to positive group (p<0.001). This study highlights that perindopril could reduce the ACE2 expression and pro-inflammatory cytokine levels in adipocytes exposed to SARS-CoV-2 S1 spike protein.
Insights
Perindopril, an angiotensin-converting enzyme 2 (ACE2) inhibitor, significantly reduced ACE2 expression and IL-6 levels in adipocytes exposed to SARS-CoV-2 spike protein. This suggests a potential therapeutic role in managing viral infections.
Area of Science:
- Endocrinology
- Virology
- Pharmacology
Background:
- Obesity is linked to increased angiotensin-converting enzyme 2 (ACE2) expression in adipose tissue, potentially facilitating viral infections like COVID-19.
- The role of ACE inhibitors, such as perindopril, in modulating ACE2 expression and its impact on viral pathogenesis remains unclear.
Purpose of the Study:
- To investigate the effect of perindopril on ACE2 expression and pro-inflammatory cytokine levels in adipocytes exposed to SARS-CoV-2 S1 spike protein.
Main Methods:
- Adipose tissues from obese male donors were enzymatically isolated and exposed to SARS-CoV-2 S1 spike protein.
- ACE2 expression was quantified using ELISA, with human recombinant ACE2 (hrsACE2) and perindopril as treatments.
- Interleukin-6 (IL-6) levels were also assessed.
Main Results:
- Exposure to SARS-CoV-2 Spike protein significantly increased ACE2 expression in adipocytes.
- Perindopril administration markedly decreased ACE2 expression (43.37 μg/mL) compared to the positive control (80.31 μg/mL) (p<0.001).
- Perindopril treatment also significantly reduced IL-6 levels (p<0.001).
Conclusions:
- Perindopril effectively reduces ACE2 expression in adipocytes stimulated by SARS-CoV-2 S1 spike protein.
- Perindopril demonstrates anti-inflammatory effects by decreasing IL-6 levels in this context.
- These findings suggest perindopril's potential therapeutic benefit in mitigating viral infections associated with elevated ACE2 expression.
Related Concept Videos
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors
Antihypertensive Drugs: Angiotensin II Receptor Blockers
Antihypertensive Drugs: Direct Renin Inhibitors
Adrenergic Receptors: β Subtype
Isoprenaline > Adrenaline > Noradrenaline
Neurotransmitter binding to these receptors causes activation of adenylyl cyclase resulting in increased concentrations of cAMP and modulation of calcium ion channels within the cell. They are further classified into β1, β2, and β3 subtypes.
β1-adrenoceptors: β1-adrenoceptors...
Adrenergic Receptors: ɑ Subtype
Adrenaline ≥ Noradrenaline >> Isoprenaline
α-adrenoceptors are further divided into α1 and α2-adrenoceptors.
α1-Adrenoceptors: These receptors are located postsynaptically on the effector organs and cause constriction of smooth muscle mediated by activation of phospholipase...
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

