The effect of grape seed proanthocyanidin extract in preventing amikacin-induced nephropathy.


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ULUSOY Ş., Özkan G., ERSÖZ Ş., ÖREM A., ALKANAT M., YUCESAN F., ...Daha Fazla

Renal failure, cilt.34, sa.2, ss.227-34, 2012 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 34 Sayı: 2
  • Basım Tarihi: 2012
  • Doi Numarası: 10.3109/0886022x.2011.643391
  • Dergi Adı: Renal failure
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.227-34
  • Anahtar Kelimeler: AG nephropathy, amikacin-induced nephropathy, grape seed proanthocyanidin, GSPE, MDA, oxidative system, GENTAMICIN-INDUCED NEPHROTOXICITY, PHENETHYL ESTER CAPE, OXIDATIVE DAMAGE, PROTECTIVE ROLE, RAT-KIDNEY, INJURY, PENTOXIFYLLINE, TOXICITY
  • Karadeniz Teknik Üniversitesi Adresli: Evet

Özet

Background/Aims: Nephrotoxicity induced by aminoglycosides (AGs) limits their clinical use. As yet, no molecules have been approved to prevent AG nephropathy. We aim to investigate the effectiveness of grape seed proanthocyanidin extract (GSPE) in the prevention of amikacin (AK)-induced nephrotoxicity. Methods: A total of 24 rats were allocated into control, GSPE, AK, and AK + GSPE groups. While 1 mL saline was administered for 6 days in control and AK groups, 100 mg/kg GSPE was administered in GSPE and AK + GSPE groups. On day 7, intraperitoneal (i.p.) saline was administered in control and GSPE groups, while 1.2 g/kg i.p. AK was administered in AK and AK + GSPE groups. The experiment was terminated on day 9. Blood samples were taken for the measurement of renal functions. Renal tissues of the rats were removed for the analysis of malondialdehyde (MDA), total oxidant system (TOS), total antioxidant system, oxidative stress index (OSI), and for histopathological examination. Results: MDA level was found to be lower in GSPE group compared with other study groups. There was significantly more renal histopathological damage and higher blood urea nitrogen, creatinine, TOS, OSI, and MDA levels in the AK group compared with the control and AK + GSPE groups. The same parameters showed significant improvement in AK + GSPE group compared with AK group. Conclusion: Our findings demonstrate for the first time that GSPE reduces oxidative damage in AK nephropathy and provides biochemical and renal histopathological improvements.