Protective effect of quercetin on the evolution of cisplatin-induced acute tubular necrosis

Kidney Blood Press Res. 2004;27(3):148-58. doi: 10.1159/000078309. Epub 2004 Apr 30.

Abstract

Background: The mechanism of cisplatin-induced nephrotoxicity is unknown, but has been associated with renal lipid peroxidation. The bioflavonoid quercetin may be a potential alternative to reduce cisplatin-induced nephrotoxicity. The aim of this study was to evaluate the effect of quercetin on the evolution of cisplatin-induced acute tubular necrosis.

Methods: One hundred and three male Wistar rats were injected with cisplatin (5 mg/kg, i.p.), 43 of them received quercetin (50 mg/kg, by gavage) before cisplatin injection. Blood and urine were collected 5 and 20 days after the injection for the determination of plasma creatinine, urine volume and osmolality. The kidneys were removed for the determination of renal malondialdehyde (MDA) and for histological and immunohistochemical studies. The renal expression of fibronectin, alpha-smooth muscle actin, vimentin, Jun N-terminal kinase, nuclear factor-kappaB, and macrophages during the evolution of the acute tubular necrosis induced by cisplatin and the histological changes observed in the kidneys were analyzed.

Results: Cisplatin-treated rats presented a transitory increase in plasma creatinine levels, tubular cell necrosis and increased immunostaining for vimentin, alpha-SM-actin, fibronectin, ED1, NF-kappaB, and p-JNK in the renal cortex and outer medulla. These alterations were less intense in animals treated with quercetin.

Conclusion: Quercetin treatment attenuated the functional, histological and immunohistochemical alterations induced by cisplatin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Antineoplastic Agents / toxicity*
  • Cisplatin / toxicity*
  • Creatine / metabolism
  • Free Radicals / metabolism
  • Immunohistochemistry
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Kidney / drug effects*
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney Tubular Necrosis, Acute / chemically induced
  • Kidney Tubular Necrosis, Acute / drug therapy*
  • Kidney Tubular Necrosis, Acute / pathology
  • Male
  • NF-kappa B / metabolism
  • Peroxidase / metabolism
  • Quercetin / pharmacology*
  • Rats
  • Rats, Wistar
  • Vimentin / metabolism

Substances

  • Actins
  • Antineoplastic Agents
  • Free Radicals
  • NF-kappa B
  • Vimentin
  • Quercetin
  • Peroxidase
  • JNK Mitogen-Activated Protein Kinases
  • Creatine
  • Cisplatin