Protective effects of naringenin on carbon tetrachloride-induced acute nephrotoxicity in mouse kidney

Chem Biol Interact. 2013 Sep 25;205(2):138-47. doi: 10.1016/j.cbi.2013.06.016. Epub 2013 Jul 9.

Abstract

The ability of naringenin (NGN) to protect the kidney against CCl4-induced renal toxicity in male Swiss mice was investigated. The flavonoid was given orally to mice for 7days and then on the 8th day, these were intraperitoneally injected with 10mmol/kg CCl4. When the toxicant was administrated alone, an increase of malondialdehyde (MDA) concentration was observed and a significant decrease in superoxide dismutase (SOD), catalase (CAT) glutathione-peroxidase (GPx) specific activities as well as glutathione (GSH) levels was detected after 24h. These were accompanied by glomerular and tubular degenerations, vascular congestion, necrosis and fatty changes. Marked collagen deposition and strong TGF-β1 expression were observed mainly in the mesangial cells of the glomeruli and tubulointerstitial areas. Ultrastructural investigations showed proximal and distal tubular epithelial cells alterations including numerous lysosomes and dense granular bodies, altered mitochondria, appearance of "myeloid bodies" and basal enfolding dilatation. Pre-treatment with NGN resulted in the return of biochemical markers to control values. Histopathological and electron-microscopic examinations confirmed the biochemical results. In conclusion, NGN showed antioxidant and renal protective effects against injuries induced by CCl4.

Keywords: Antioxidant effects; CCl(4); Naringenin; Nephroprotection; Oxidative stress.

MeSH terms

  • Acute Kidney Injury / metabolism
  • Acute Kidney Injury / pathology
  • Acute Kidney Injury / prevention & control*
  • Animals
  • Antioxidants / pharmacology*
  • Carbon Tetrachloride / antagonists & inhibitors
  • Carbon Tetrachloride / toxicity
  • Flavanones / pharmacology*
  • Hepatitis A Virus Cellular Receptor 1
  • Kidney / drug effects*
  • Kidney / metabolism
  • Kidney / pathology
  • Lipid Peroxidation / drug effects
  • Male
  • Membrane Proteins / metabolism
  • Mice
  • Microscopy, Electron, Transmission
  • Transforming Growth Factor beta1 / metabolism

Substances

  • Antioxidants
  • Flavanones
  • Havcr1 protein, mouse
  • Hepatitis A Virus Cellular Receptor 1
  • Membrane Proteins
  • Transforming Growth Factor beta1
  • Carbon Tetrachloride
  • naringenin