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What about COVID-19 and arachidonic acid pathway?
- Source :
-
European journal of clinical pharmacology [Eur J Clin Pharmacol] 2020 Nov; Vol. 76 (11), pp. 1501-1504. Date of Electronic Publication: 2020 Jun 25. - Publication Year :
- 2020
-
Abstract
- Background and Objective: COVID-19 is a highly contagious viral disease. In this study, we tried to define and discuss all the findings on the potential association between arachidonic acid (AA) pathway and COVID-19 pathophysiology.<br />Methods: A literature search across PubMed, Scopus, Embase, and Cochrane database was conducted. A total of 25 studies were identified.<br />Results: The data elucidated that COX-2 and prostaglandins (PGs), particularly PGE <subscript>2</subscript> , have pro-inflammatory action in COVID-19 pathophysiology. Arachidonic acid can act as endogenous antiviral compound. A deficiency in AA can make humans more susceptible to COVID-19. Targeting these pro-inflammatory mediators may help in decreasing the mortality and morbidity rate in COVID-19 patients.<br />Conclusions: PGE <subscript>2</subscript> levels and other PGs levels should be measured in patients with COVID-19. Lowering the PGE <subscript>2</subscript> levels through inhibition of human microsomal prostaglandin E synthase-1 (mPGES-1) can enhance the host immune response against COVID-19. In addition, the hybrid compounds, such as COX-2 inhibitors/TP antagonists, can be an innovative treatment to control the overall balance between AA mediators in patients with COVID-19.
- Subjects :
- Anti-Inflammatory Agents, Non-Steroidal pharmacology
Betacoronavirus
COVID-19
Cyclooxygenase 2 blood
Humans
Pandemics
Phospholipases A2 biosynthesis
Prostaglandin-E Synthases blood
Prostaglandins biosynthesis
Prostaglandins blood
Protein-Lysine 6-Oxidase biosynthesis
SARS-CoV-2
Sex Factors
Arachidonic Acid biosynthesis
Coronavirus Infections physiopathology
Cyclooxygenase 2 biosynthesis
Inflammation metabolism
Pneumonia, Viral physiopathology
Prostaglandin-E Synthases biosynthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1432-1041
- Volume :
- 76
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- European journal of clinical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 32583353
- Full Text :
- https://doi.org/10.1007/s00228-020-02941-w