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.

Narra J
|September 16, 2024
PubMed

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.

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