Lipopolysaccharide impairs hepatocyte ureagenesis from ammonia: involvement of mitochondrial aquaporin-8

FEBS Lett. 2014 May 2;588(9):1686-91. doi: 10.1016/j.febslet.2014.03.012. Epub 2014 Mar 15.

Abstract

We recently reported that hepatocyte mitochondrial aquaporin-8 (mtAQP8) channels facilitate the uptake of ammonia and its metabolism into urea. Here we studied the effect of bacterial lipopolysaccharides (LPS) on ammonia-derived ureagenesis. In LPS-treated rats, hepatic mtAQP8 protein expression and diffusional ammonia permeability (measured utilizing ammonia analogues) of liver inner mitochondrial membranes were downregulated. NMR studies using 15N-labeled ammonia indicated that basal and glucagon-induced ureagenesis from ammonia were significantly reduced in hepatocytes from LPS-treated rats. Our data suggest that hepatocyte mtAQP8-mediated ammonia removal via ureagenesis is impaired by LPS, a mechanism potentially relevant to the molecular pathogenesis of defective hepatic ammonia detoxification in sepsis.

Keywords: Aquaporin-8; Llipopolysaccharide; Mitochondrial ammonia transport; Urea synthesis; hepatocyte.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ammonia / metabolism*
  • Animals
  • Aquaporins / metabolism*
  • Biological Transport
  • Cells, Cultured
  • Glucagon / physiology
  • Hepatocytes / immunology
  • Hepatocytes / metabolism*
  • Lipopolysaccharides / pharmacology*
  • Male
  • Methylamines / metabolism
  • Mitochondria, Liver / immunology
  • Mitochondria, Liver / metabolism*
  • Rats
  • Rats, Wistar
  • Urea / metabolism*

Substances

  • Aquaporins
  • Lipopolysaccharides
  • Methylamines
  • aquaporin 8
  • Ammonia
  • Urea
  • Glucagon
  • methylamine