Bioactive Lipids in COVID-19-Further Evidence

Undurti N Das1

  • 1UND Life Sciences, Battle Ground, WA, USA; BioScience Research Centre and Department of Medicine, GVP Medical College and Hospital, Visakhapatnam, India.

Archives of Medical Research
|September 28, 2020
PubMed

Insights

Arachidonic acid (AA) and bioactive lipids (BALs) may prevent and treat COVID-19 by inactivating SARS-CoV-2. Low levels of AA and lipoxin A4 (LXA4) are linked to increased COVID-19 severity in vulnerable populations.

Area of Science:

  • Biochemistry
  • Immunology
  • Virology

Background:

  • Macrophages and T cells release arachidonic acid (AA) and bioactive lipids (BALs) to combat microbes.
  • Pro-inflammatory (PGE2, LTs) and anti-inflammatory (LXA4, resolvins, protectins, maresins) metabolites derived from AA and omega-3 fatty acids modulate macrophage polarization.
  • AA, PGE2, LXA4, and other BALs inhibit pro-inflammatory cytokines like IL-6 and TNF-α.

Purpose of the Study:

  • To investigate the potential of AA and BALs in preventing and treating COVID-19.
  • To explore the role of AA and BALs in SARS-CoV-2 inactivation and their impact on immune responses.
  • To examine the association between low AA and LXA4 levels and susceptibility to severe COVID-19.

Main Methods:

  • Review of existing observations and literature supporting the role of BALs in microbial inactivation and immune modulation.
  • Analysis of the influence of AA and BALs on cytokine synthesis and macrophage polarization.
  • Examination of the link between AA, LXA4 levels, and COVID-19 risk factors like metabolic diseases and age.

Main Results:

  • AA and BALs inactivate SARS-CoV-2 and various microbes.
  • BALs influence the generation of M1 and M2 macrophages and inhibit key pro-inflammatory cytokines.
  • Low plasma concentrations of AA and LXA4 are observed in individuals with insulin resistance, obesity, diabetes, hypertension, heart disease, and the elderly, potentially increasing their COVID-19 susceptibility.
  • Mesenchymal stem cells (MSCs) utilize LXA4 for therapeutic effects in COVID-19.
  • Drugs like statins, colchicine, and corticosteroids may affect BALs metabolism.
  • AA and BALs regulate cell membrane fluidity and ACE-2 receptor expression.

Conclusions:

  • Administration of BALs, particularly AA, could be beneficial for preventing and managing COVID-19 and other enveloped viral infections.
  • Maintaining adequate levels of AA and LXA4 may be crucial for mitigating COVID-19 severity, especially in at-risk populations.
  • Further research into BALs as therapeutic agents for viral infections is warranted.

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