Suppression of renal alpha-dicarbonyl compounds generated following ureteral obstruction by kidney-specific alpha-dicarbonyl/L-xylulose reductase

Ann N Y Acad Sci. 2008 Apr:1126:320-4. doi: 10.1196/annals.1433.003. Epub 2007 Dec 13.

Abstract

Renal unilateral ureteral obstruction (UUO) causes acute generation of alpha-dicarbonyl stress substances, such as glyoxal, 3-deoxyglucosone, and methylglyoxal, in the kidneys. These alpha-dicarbonyl compounds are prone to form advanced glycation end products (AGEs) via the nonenzymatic Maillard reaction. Using transgenic (Tg) mice overexpressing a kidney-specific short-chain oxidoreductase, alpha-dicarbonyl/L-xylulose reductase (DCXR), we measured generation of alpha-dicarbonyls following UUO by means of electrospray ionization/liquid chromatography/mass spectrometry in their kidney extracts. The accumulation of 3-deoxyglucosone was significantly reduced in the kidneys of the mice Tg for DCXR compared to their wild-type littermates, demonstrating 4.91 +/- 2.04 vs. 6.45 +/- 1.85 ng/mg protein (P = 0.044) for the obstructed kidneys, and 3.68 +/- 1.95 vs. 5.20 +/- 1.39 ng/mg protein (P = 0.026) for the contralateral kidneys. Despite the reduction in accumulated alpha-dicarbonyls, collagen III content in kidneys of the Tg mice and their wild-type littermates showed no difference as monitored by in situ hybridization. Collectively, DCXR may function in the removal of renal alpha-dicarbonyl compounds under oxidative circumstances, but it is not sufficient to suppress acute renal fibrosis during 7 days UUO.

MeSH terms

  • Animals
  • Fibrosis
  • Glyoxal / analogs & derivatives*
  • Glyoxal / metabolism
  • Humans
  • Kidney / enzymology
  • Kidney / metabolism*
  • Kidney Diseases / enzymology
  • Kidney Diseases / pathology
  • Mice
  • Mice, Transgenic
  • Sugar Alcohol Dehydrogenases / genetics*
  • Sugar Alcohol Dehydrogenases / metabolism*
  • Ureteral Obstruction / enzymology
  • Ureteral Obstruction / etiology*

Substances

  • alpha-dicarbonyl methylglyoxal
  • Glyoxal
  • Sugar Alcohol Dehydrogenases
  • L-xylulose reductase