Protective effects of vitamin e and probucol against gentamicin-induced nephrotoxicity in rats

A B Abdel-Naim1, M H Abdel-Wahab, F F Attia

  • 1Department of Pharmacology and Toxicology, Faculty of Pharmacy, Al-Azhar University, Nasr City, Cairo, Egypt.

Insights

Vitamin E and probucol protect against gentamicin (GM) nephrotoxicity by reducing oxidative stress. These antioxidants significantly improved kidney function markers and reduced kidney damage in rats treated with GM.

Area of Science:

  • Pharmacology
  • Toxicology
  • Biochemistry

Background:

  • Gentamicin (GM) is a crucial antibiotic for severe gram-negative infections.
  • GM-induced nephrotoxicity is a significant clinical limitation, potentially mediated by reactive oxygen species.
  • Vitamin E and probucol are antioxidants with potential protective properties.

Purpose of the Study:

  • To investigate the protective effects of vitamin E and/or probucol against gentamicin-induced nephrotoxicity in rats.
  • To evaluate the role of antioxidant activity in mitigating GM-induced kidney damage.

Main Methods:

  • Rats received a single dose of gentamicin (150 mg/kg).
  • Vitamin E (250 mg/kg) and/or probucol (60 mg/kg) were administered daily for 3 days prior to gentamicin.
  • Nephrotoxicity was assessed by measuring serum urea, creatinine, urinary NAG and gamma-GT, and kidney malondialdehyde (MDA), non-protein sulphydryls (NPSH), and superoxide dismutase (SOD) activity.

Main Results:

  • Gentamicin significantly increased serum urea, creatinine, urinary NAG/gamma-GT, and kidney MDA, while decreasing kidney NPSH and SOD activity.
  • Vitamin E and probucol pretreatment significantly reduced these markers of nephrotoxicity.
  • Combined vitamin E and probucol showed enhanced protective effects against GM-induced kidney damage.

Conclusions:

  • Vitamin E and probucol exhibit significant protective effects against gentamicin nephrotoxicity in rats.
  • Their antioxidant properties are key mechanisms underlying the observed renal protection.
  • These findings suggest potential therapeutic strategies to mitigate gentamicin-induced kidney injury.