[Effects of astaxanthin on renal fibrosis and cell apoptosis induced by partial unilateral ureteral obstruction in rats]

Nan Fang Yi Ke Da Xue Xue Bao. 2013 Feb;33(2):305-8.
[Article in Chinese]

Abstract

Objective: To study the effects of astaxanthin on renal fibrosis and apoptosis induced by partial unilateral ureteral obstruction (UUO) in rats.

Methods: Ninety-six male adult SD rats were randomized into 6 equal groups, namely the blank control group, sham-operated group, UUO group, and astaxanthin group at high, medium, and low doses. Left ureteral ligation was performed in UUO and astaxanthin groups, and two days before the operation, the rats in astaxanthin groups were lavaged with 25, 50, or 100 mg/kg astaxanthin daily for 14 days, while the same volume of saline was given to rats in UUO group and sham-operated group. Renal pathological in the rats was observed with HE staining, and the expression levels of TGF-β1, SGK1, and CTGF in the left kidney were detected immunohistochemically; the expression level of Bcl-2 and Bax were detected using Bcl-2 and Bax detection kits.

Results: Compared to UUO group, high- and medium-dose astaxanthin groups showed obviously ameliorated renal pathologies and reduced expressions of TGF-β1, SGK1, and CTGF in the left kidney with lessened renal cell apoptosis.

Conclusion: Astaxanthin can reduce UUO-induced renal fibrosis and renal cell apoptosis, demonstrating the renoprotective effect of astaxanthin against renal fibrosis.

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Connective Tissue Growth Factor / metabolism
  • Fibrosis
  • Immediate-Early Proteins / metabolism
  • Kidney / drug effects
  • Kidney / metabolism
  • Kidney / pathology*
  • Kidney Diseases / metabolism
  • Kidney Diseases / pathology*
  • Male
  • Protein Serine-Threonine Kinases / metabolism
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Transforming Growth Factor beta1 / metabolism
  • Ureteral Obstruction / metabolism
  • Ureteral Obstruction / pathology*
  • Xanthophylls / pharmacology
  • bcl-2-Associated X Protein / metabolism

Substances

  • Bax protein, rat
  • CCN2 protein, rat
  • Immediate-Early Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Tgfb1 protein, rat
  • Transforming Growth Factor beta1
  • Xanthophylls
  • bcl-2-Associated X Protein
  • Connective Tissue Growth Factor
  • astaxanthine
  • Protein Serine-Threonine Kinases
  • serum-glucocorticoid regulated kinase