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Oxidative Stress and Renal Dysfunction in Lincomycin-Induced Nephrotoxicity: Evaluating the Therapeutic Potential of Activated Charcoal

Author

Listed:
  • Sarah Ebutte

    (Department of Anatomy, College of Health Sciences, Benue State University, Makurdi, Nigeria)

  • Gabriel Idoko

    (Department of Anatomy, College of Health Sciences, Benue State University, Makurdi, Nigeria)

  • Vershima Kiekwe

    (Department of Anatomy, College of Health Sciences, Benue State University, Makurdi, Nigeria)

  • Peter Onoja

    (Department of Anatomy, College of Health Sciences, Benue State University, Makurdi, Nigeria)

  • Paul Beega

    (Department of Anatomy, College of Health Sciences, Benue State University, Makurdi, Nigeria)

  • Thaedeus Aende

    (Department of Anatomy, College of Health Sciences, Benue State University, Makurdi, Nigeria)

  • Moses Mlumun

    (Department of Anatomy, College of Health Sciences, Benue State University, Makurdi, Nigeria)

  • Gabriel Akunna

    (Department of Anatomy, College of Health Sciences, Benue State University, Makurdi, Nigeria)

  • Linus Saalu

    (Department of Anatomy, College of Health Sciences, Benue State University, Makurdi, Nigeria)

Abstract

Background: The kidneys play a vital role in homeostasis and metabolic waste elimination, but they are highly susceptible to toxic insults due to their role in drug metabolism. Lincomycin, a lincosamide antibiotic, has been implicated in nephrotoxicity through oxidative stress-mediated mechanisms, leading to renal dysfunction. Activated charcoal, a widely used adsorbent, has shown potential in mitigating renal damage by adsorbing toxins and modulating oxidative stress. However, its efficacy in lincomycin-induced nephrotoxicity remains poorly understood. Aim: This study investigates the protective potential of activated charcoal against lincomycin-induced nephrotoxicity by assessing oxidative stress markers, renal function indices, and histopathological changes. Methodology: Twenty-five (25) Wistar rats were divided into five groups (n=5). Group I (Control) received normal saline, while Group II received lincomycin (200 mg/kg). Groups III, IV, and V were co-administered lincomycin with varying percentages of activated charcoal (25%, 50%, and 75%). Kidney function markers (creatinine, urea), oxidative stress indices (Superoxide Dismutase [SOD], Malondialdehyde [MDA]), and histopathological changes were evaluated. Results: Lincomycin administration significantly reduced creatinine (0.59±0.07 mg/dl) and urea (19.85±2.11 mg/dl) compared to controls (0.85±0.04 mg/dl, 25.78±1.19 mg/dl; P

Suggested Citation

  • Sarah Ebutte & Gabriel Idoko & Vershima Kiekwe & Peter Onoja & Paul Beega & Thaedeus Aende & Moses Mlumun & Gabriel Akunna & Linus Saalu, 2025. "Oxidative Stress and Renal Dysfunction in Lincomycin-Induced Nephrotoxicity: Evaluating the Therapeutic Potential of Activated Charcoal," Journal of Innovations in Medical Research, Paradigm Academic Press, vol. 4(4), pages 1-12, August.
  • Handle: RePEc:bdz:joimer:v:4:y:2025:i:4:p:1-12
    DOI: 10.63593/JIMR.2788-7022.2025.08.001
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