Changes of renal vitamin D metabolic enzyme expression and calcium transporter abundance in obstructive nephropathy

Nephrology (Carlton). 2011 Nov;16(8):710-4. doi: 10.1111/j.1440-1797.2011.01495.x.

Abstract

The effects of urinary-tract obstruction on renal function have been clarified. However, there is little known about the change of renal vitamin D metabolic enzyme expression and vitamin D-dependent calcium transporting proteins expression in obstructive nephropathy. The male mice were subjected to unilateral ureteral obstruction (n = 10) or sham operation (n = 10). All mice were killed on day 7 after the surgical operation. Kidney sections were stained with Masson's trichrome and gene expression was analyzed by reverse transcription-polymerase chain reaction (RT-PCR) and real-time PCR. The obstructed kidney exhibited interstitial fibrosis as shown by the strong collagen deposition in the interstitium. Quantitative PCR results showed the increase of 1-OHase (P < 0.001) mRNA expression and the decrease of 24-OHase (P < 0.01), CaBP-9k (P < 0.01) and CaBP-28k (P < 0.01) mRNA expression in obstructed kidney as compared to that of the Sham group. In addition, the mRNA expression of 1-OHase and CaBP-9k was significantly increased and decreased, respectively, in obstructed kidney as compared to that of the contra-lateral kidney in unilateral ureteral obstruction (UUO) mice. Together, the present finding supports the hypothesis that the ureteral obstruction leads to the alteration of renal vitamin D metabolic enzyme expression and calcium transporter abundance, which may secondarily induce the abnormality of vitamin D endocrine system and bone health.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calbindins
  • Calcium / blood
  • Calcium Channels / metabolism
  • Calcium-Transporting ATPases / metabolism
  • Disease Models, Animal
  • Gene Expression Regulation, Enzymologic / physiology
  • Kidney / enzymology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • S100 Calcium Binding Protein G / metabolism*
  • Steroid 21-Hydroxylase / metabolism*
  • Steroid Hydroxylases / metabolism*
  • TRPV Cation Channels / metabolism
  • Ureteral Obstruction / metabolism*
  • Ureteral Obstruction / physiopathology
  • Vitamin D / metabolism*
  • Vitamin D3 24-Hydroxylase

Substances

  • Calbindins
  • Calcium Channels
  • S100 Calcium Binding Protein G
  • TRPV Cation Channels
  • Trpv5 protein, mouse
  • Vitamin D
  • Steroid Hydroxylases
  • Cyp21a1 protein, mouse
  • Steroid 21-Hydroxylase
  • Vitamin D3 24-Hydroxylase
  • Calcium-Transporting ATPases
  • Calcium