Review of Clinical Pharmacology and Pharmacokinetics – International Edition Volume 38 (2024) – Supplementary Issue 2

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Beneficial effect of Alhagi maurorum on rats submitted to sulfadimidine-induced kidney injury
Nada Mahdi Alkhafaji1, Hussein Jasim Alharbi1*

1Department of Biology, College of Science, University of Babylon, Hillah, Iraq


*Corresponding author:
Hussein Jasim Alharbi, Department of Biology, College of Science, University of Babylon, Hillah, Iraq; Tel.: +964-(0)7811436990
E-mail: husseinjasim1967@gmail.com


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Published: 5 May 2024; https://doi.org/10.61873/HNKR5864

Abstract

Alhagi maurorum is one of the many plants that have proven effectiveness in folklore medicine and that are still utilized to treat disease or disorders, thanks to their phytochemical compounds and other secondary metabolites. Sulfadimidine, chemical known as 4-amino-N-(4,6-dimethylpyrimidin-2-yl)benzene-sulfonamide, is an antibacterial drug that has side-effects on organs such as the kidney. In this study, the unwanted acute effect of this sulfonamide and of its metabolites was recorded in the form of rat interstitial nephritis and as an increase in creatinine and blood urea nitrogen (BUN) levels. Results showed a significant (P<0.05) decrease in BUN levels in rat groups treated with the ethanolic extract of Alhagi maurorum as a therapy, but there were no significant differences observed in terms of the creatinine levels in these groups. The undertaken histological study revealed an almost normal histological appearance of the kidneys in the two groups of rats that were treated with the plant extract as a therapy after the damage that occurred as a result of the drug injection (interstitial nephritis, infiltration lymphocytes, and mild tubular atrophy). Our study suggests a potential benefit from natural plants in the treatment of drug-related adverse effects.

Keywords: Alhagi maurorum, sulfadimidine, kidney damage, creatinine, rat

Please cite as:
Alkhafaji N.M., Alharbi H.J. Beneficial effect of Alhagi maurorum on rats submitted to sulfadimidine-induced kidney injury. Rev. Clin. Pharmacol. Pharmacokinet. Int. Ed. 38(Sup2): 81-84 (2024). https://doi.org/10.61873/HNKR5864

 

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