Back to Search Start Over

Melatonin alleviates arsenic‐induced liver injury by regulating protein RKIP and enhancing antioxidant defencse mechanisms.

Authors :
Rezvankhah, Soheil
Zargari, Felor
Sharifi, Rasoul
Source :
Journal of Biochemical & Molecular Toxicology; Sep2024, Vol. 38 Issue 9, p1-5, 5p
Publication Year :
2024

Abstract

Arsenic (As) is a highly toxic metal and one of the main factors in cancer development through oxidative stress and production of reactive oxygen species. Prior research has demonstrated melatonin's potential as a free radical scavenger. Raf kinase inhibitory protein (RKIP) is an important regulator of intracellular signaling pathways that has been linked to various types of cancer. The aim of this research was to explore the influence of melatonin's antioxidant properties on the expression of the protein RKIP and the antioxidant status of liver tissue in rats that were exposed to arsenic. Thirty two male Wistar rats were divided into four groups of eight, including control, melatonin‐treated (20 mg/Kg of melatonin), sodium arsenite‐treated (5.5 mg/Kg of sodium arsenite), and melatonin + sodium arsenite‐treated groups (combination) for 4 weeks. The expression level of protein RKIP was measured by Western blot, and malondialdehyde (MDA) content of the liver as well as the activities of antioxidant enzymes were measured. The data analyzed using one‐way ANOVA (significance level of p < 0.05) and GraphPad Prism (9) software. Sodium arsenite treatment led to a significant decrease in RKIP protein expression and antioxidant enzyme activity, and an increase in liver MDA levels (p < 0.001). Conversely, melatonin treatment in the combination group resulted in a significant increase in RKIP protein expression and antioxidant enzyme activity and a decrease in liver MDA levels (p < 0.05). These findings suggest that melatonin can attenuate oxidative damage caused by arsenic in liver cells by enhancing RKIP protein expression and antioxidant enzyme activity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10956670
Volume :
38
Issue :
9
Database :
Complementary Index
Journal :
Journal of Biochemical & Molecular Toxicology
Publication Type :
Academic Journal
Accession number :
179550503
Full Text :
https://doi.org/10.1002/jbt.23835