» Articles » PMID: 37139624

Protective Effects of Vitamin D (cholecalciferol) on Vancomycin-induced Oxidative Nephrotoxic Damage in Rats

Overview
Journal Pharm Biol
Specialties Pharmacology
Pharmacy
Date 2023 May 4
PMID 37139624
Authors
Affiliations
Soon will be listed here.
Abstract

Context: Vancomycin (VCM), an important antibiotic against refractory infections, has been used to treat secondary infections in severe COVID-19 patients. Regrettably, VCM treatment has been associated with nephrotoxicity. Vitamin D can prevent nephrotoxicity through its antioxidant effect.

Objective: This study tests the antioxidant effect of vitamin D in the prevention of VCM-induced nephrotoxicity.

Materials And Methods: Wistar Albino rats (21) were randomly divided into 3 groups: (A) control; (B) VCM 300 mg/kg daily for 1 week; and (C) VCM plus vitamin D 500 IU/kg daily for 2 weeks. All the rats were sacrificed and serum was separated to determine kidney function parameters. Their kidneys were also dissected for histological examination and for oxidative stress markers.

Results: Lipid peroxidation, creatinine, and urea levels decreased significantly ( < 0.0001) in the vitamin D-treated group (14.46, 84.11, 36.17%, respectively) compared to the VCM group that was given VCM (MIC<2 μg/mL) only. A significant increase was observed in superoxide dismutase levels in the vitamin D-treated group ( < 0.05) compared to rats without treatment. Furthermore, kidney histopathology of the rats treated with vitamin D showed that dilatation, vacuolization and necrosis tubules decreased significantly ( < 0.05) compared with those in the VCM group. Glomerular injury, hyaline dystrophy, and inflammation improved significantly in the vitamin D group ( < 0.001,  < 0.05,  < 0.05, respectively) compared with the VCM group.

Discussion And Conclusions: Vitamin D can prevent VCM nephrotoxicity. Therefore, the appropriate dose of this vitamin must be determined, especially for those infected with COVID-19 and receiving VCM, to manage their secondary infections.

Citing Articles

Potential therapeutic impacts of vitamin D on hypothyroid-induced heart and kidney fibrosis and oxidative status in male rat.

Rastegar-Moghaddam S, Akbarian M, Rajabian A, Alipour F, Hojjati Shargh A, Masoomi R Naunyn Schmiedebergs Arch Pharmacol. 2024; .

PMID: 39535596 DOI: 10.1007/s00210-024-03593-8.


Advances in nephroprotection: the therapeutic role of selenium, silver, and gold nanoparticles in renal health.

Karunakar K, Edwin E, Gopalakrishnan M, Cheriyan B, Ramaiyan V, Karthikha V Int Urol Nephrol. 2024; 57(2):479-510.

PMID: 39312019 DOI: 10.1007/s11255-024-04212-4.


The Role of Vitamin D in Neuroprotection in Multiple Sclerosis: An Update.

Sangha A, Quon M, Pfeffer G, Orton S Nutrients. 2023; 15(13).

PMID: 37447304 PMC: 10346708. DOI: 10.3390/nu15132978.

References
1.
DeLuca H, Cantorna M . Vitamin D: its role and uses in immunology. FASEB J. 2001; 15(14):2579-85. DOI: 10.1096/fj.01-0433rev. View

2.
Ocak S, Gorur S, Hakverdi S, Celik S, Erdogan S . Protective effects of caffeic acid phenethyl ester, vitamin C, vitamin E and N-acetylcysteine on vancomycin-induced nephrotoxicity in rats. Basic Clin Pharmacol Toxicol. 2007; 100(5):328-33. DOI: 10.1111/j.1742-7843.2007.00051.x. View

3.
Jorgensen S, Murray K, Lagnf A, Melvin S, Bhatia S, Shamim M . A Multicenter Evaluation of Vancomycin-Associated Acute Kidney Injury in Hospitalized Patients with Acute Bacterial Skin and Skin Structure Infections. Infect Dis Ther. 2020; 9(1):89-106. PMC: 7054514. DOI: 10.1007/s40121-019-00278-1. View

4.
Bouillon R, Carmeliet G, Verlinden L, van Etten E, Verstuyf A, Luderer H . Vitamin D and human health: lessons from vitamin D receptor null mice. Endocr Rev. 2008; 29(6):726-76. PMC: 2583388. DOI: 10.1210/er.2008-0004. View

5.
Kim D, Meza C, Clarke H, Kim J, Hickner R . Vitamin D and Endothelial Function. Nutrients. 2020; 12(2). PMC: 7071424. DOI: 10.3390/nu12020575. View