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©The Author(s) 2021.
World J Gastroenterol. Dec 28, 2021; 27(48): 8370-8373
Published online Dec 28, 2021. doi: 10.3748/wjg.v27.i48.8370
Published online Dec 28, 2021. doi: 10.3748/wjg.v27.i48.8370
Name | Type | Mechanisms as anti-COVID-19 drugs and/or drugs for drug-induced liver injury | Mechanisms of hepatotoxicity | Ref. |
Anti-COVID-19 drugs | ||||
Dexamethasone | Anti-inflammatory drug | Amelioration of inflammatory organ injury in viral pneumonia. Alleviation of tissue damage caused by inflammatory responses of the immune system within the liver. | Drug-drug interactions due to cytochrome P450 induction. Elevation of liver enzyme levels, increase in hepatic lipid peroxidation, and decrease in antioxidant activities. | [2,6,7] |
Remdesivir | Antiviral drug | Inhibition of RNA polymerase, as a nucleotide analog. | Hepatocellular toxicity. | [10] |
Drugs for drug-induced liver injury | ||||
Glycyrrhizic acid | Hepatoprotector | Regulation of the expression of hepatobiliary membrane transporters. | [12] | |
Ursodeoxycholic acid | Hepatoprotector | Anti-inflammatory, antioxidant, immunomodulatory and antiapoptotic profiles. Inhibition of proinflammatory cytokine production. | [14] |
- Citation: Sato K, Yamazaki Y, Uraoka T. Strategy for the control of drug-induced liver injury due to investigational treatments/drugs for COVID-19. World J Gastroenterol 2021; 27(48): 8370-8373
- URL: https://www.wjgnet.com/1007-9327/full/v27/i48/8370.htm
- DOI: https://dx.doi.org/10.3748/wjg.v27.i48.8370