Proanthocyanidin alleviates vancomycin-induced kidney injury via modulation of Nrf2/Keap1/HO1, Bax/Bcl-2/Caspase-3,

Gokhan Akcakavak1, Ozhan Karatas2, Filiz Kazak Akcakavak3

  • 1Department of Pathology, Faculty of Veterinary Medicine, Aksaray University, Aksaray, Turkiye.

Tissue & Cell
|March 15, 2026
PubMed

Insights

Proanthocyanidin (PRO) protects against vancomycin-induced kidney damage by reducing oxidative stress and inflammation. This study shows PRO may be an effective treatment for vancomycin nephrotoxicity.

Area of Science:

  • Pharmacology and Toxicology
  • Nephrology
  • Biochemistry

Background:

  • Vancomycin (VAN) is crucial for treating resistant Gram-positive infections.
  • High doses of VAN cause nephrotoxicity, limiting its clinical use.
  • The protective effect of proanthocyanidin (PRO) against VAN-induced kidney damage is not well understood.

Purpose of the Study:

  • To evaluate the protective effects of PRO against VAN-induced nephrotoxicity.
  • To elucidate the underlying mechanisms of PRO's renoprotective action.

Main Methods:

  • Wistar albino rats were administered VAN (nephrotoxic agent) and/or PRO for 7 days.
  • Kidney function, oxidative stress markers, apoptosis markers, inflammatory markers, and specific signaling pathways were assessed.

Main Results:

  • PRO significantly alleviated VAN-induced kidney damage, oxidative stress, and lipid peroxidation.
  • PRO upregulated antioxidant enzymes (SOD, CAT, GPx) via the Nrf2/Keap1/HO1 pathway.
  • PRO reduced apoptosis and inflammation by modulating p53, Bax, Bcl-2, caspase-3, TLR4, NF-κB, and cytokine levels.
  • PRO treatment preserved kidney function and structure, upregulating PPARγ and downregulating GRP78.

Conclusions:

  • Proanthocyanidin demonstrates significant renoprotective effects against vancomycin-induced nephrotoxicity.
  • PRO mitigates kidney injury by inhibiting oxidative stress, inflammation, apoptosis, and ER stress.
  • PRO activates protective cellular pathways (Nrf2/HO1, PPARγ), suggesting its potential as a therapeutic agent for vancomycin nephrotoxicity.

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