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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.
Abstract:
Vancomycin (VAN), a complex tricyclic glycopeptide antibiotic, is currently utilized primarily in the therapy of bacterial infections for drug resistant Gram-positive bacteria. However, its clinical usage is restricted due to its association with renal toxicity at high doses. The potential efficacy of proanthocyanidin (PRO) on vancomycin-associated nephrotoxicity remains unclear. This current research aimed to assess the potential protective impacts of proanthocyanidin against vancomycin-associated nephrotoxicity and to assess the underlying mechanism. Wistar albino rats were split into 4 groups (8 rats per group) at random: Control (C), PRO (200 mg/kg/po), VAN (200 mg/kg, i.p., twice a day), and VAN+PRO (200 mg/kg, i.p., twice a day VAN, 200 mg/kg/po PRO). All administrations were applied for 7 days. PRO treatment alleviated VAN-induced oxidative stress by increasing antioxidants (SOD, CAT, GPx) and reducing elevated MDA levels, a marker of lipid peroxidation. PRO elevated antioxidant activity by triggering the Nrf2/Keap1/HO1 signaling pathway. VAN-induced elevations in proapoptotic p53, Bax, and caspase-3 levels were diminished by PRO, while the decrease in antiapoptotic Bcl-2 levels elevated, thereby alleviating apoptosis. Furthermore, VAN-induced increases in TLR4, MyD88, NF-κB, iNOS, IL-18, and TNF-α levels were reduced by PRO, while IL-10 levels increased, reducing the inflammatory response. PRO treatment caused an upregulation of PPARγ levels and a downregulation of GRP78 levels. Furthermore, PRO treatment preserved kidney function and structural integrity. Considering all these findings, proanthocyanidin may be effective in reducing vancomycin-induced renal injury by diminishing oxidative stress, inflammation, apoptosis, and ER stress in vancomycin-induced renal damage and activating protective cellular mechanisms through Nrf2/HO1 and PPARγ, and therefore can be considered an effective treatment option.
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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