Effect of Ocimum basilicum leaves extract on
acetaminophen-induced nephrotoxicity in
BALB/c mice
Abstract
Abstract:
Background: Acetaminophen (APAP) is one of the most widely used drugs to treat pain. Its overdose is lethal
causing liver and kidney failure. Nephrotoxicity and hepatotoxicity are mostly due to the overproduction of
reactive oxygen species. Ocimum basilicum, known as basil, is a commonly used medicinal plant due to its versatile
role as antibacterial, antifungal, and anti-oxidative. We aim in this study to investigate the preventive and
protective effect of basil leaves aqueous extract against APAP-induced hepatorenal toxicity in BALB/c mice.
Methods: Acute kidney injury (AKI) was induced in mice using APAP. Mice were treated with basils extract
pre and post AKI induction. Kidney and liver functions were assessed by measuring creatinine, urea, alanine
transaminase, and aspartate transaminase levels in serum. Superoxide dismutase, catalase (CAT), and malondialdehyde
levels of renal and hepatic tissues were assayed using Elisa. Kidney injury molecule (KIM-1) was
quantified in kidney homogenate. Histopathological analysis of kidney and liver were examined.
Results: Significant increase in all serum parameters, in hepatic and renal MDA, and in renal KIM-1 levels was
observed post AKI induction. Treatment with basils post AKI induction minimized APAP damage by reducing
serum markers and MDA in both organs and by increasing SOD and CAT. However, pretreatment with basils
extract caused additional increase in serum ALT and AST and MDA in liver, with a significant increase in renal
antioxidant enzymes. These results were confirmed by histopathological examination.
Conclusion: Basil extract may act as a natural antioxidant to treat APAP-induced acute hepato-renal toxicity
when used as a post-treatment.
Keywords: acetaminophen, hepatotoxicity, Lamiaceae, nephrotoxicity, Ocimum basilicum, oxidative damage
Coauthor(s)
Hajar Karaali, Ragaee Fahmi
Journal/Conference Information
Journal of Complementary and Integrative Medicine,DOI: DOI: 10.1515/jcim-2018-0111, ISSN: PMID: 30312166, Volume: PMID: 30312166, Issue: oct 12 2018, Pages Range: 1-15,