Morphologic effects of sulfur-substituted fatty acids on rat hepatocytes with special reference to proliferation of peroxisomes and mitochondria

J Struct Biol. 1990 May;103(3):257-65. doi: 10.1016/1047-8477(90)90044-d.

Abstract

The morphologic effects of different sulfur-substituted mono- and dicarboxylic fatty acids on rat hepatocytes have been examined. The substance 1,10-biscarboxymethylthiodecane (BCMTD) is blocked for both beta- and omega-oxidation, whereas 1-monocarboxymethylthiodecane (CMTTD) is only non-beta-oxidizable. At equimolar doses BCMTD was considerably more potent than CMTTD in hypertrophic liver enlargement. At the ultrastructural level, BCMTD increased the volume fraction of the peroxisomes by a factor of 8, and their size and number by factors of 2.1 and 6.4, respectively. Furthermore, the frequency of dense cores in the peroxisomes decreased from 60 to 8%. CMTTD resulted in an increased volume fraction of peroxisomes (4.5-fold), in the mean volume (1.9-fold), and in the number of peroxisomes (3.7-fold). At the mitochondrial level, a gradual development toward megamitochondria was observed after CMTTD administration. BCMTD, however, increased the number of mitochondria but they tended to be smaller. Administration of both acids increased peroxisomal beta-oxidation and mitochondrial carnitine palmitoyltransferase activity, whereas the lipid content of hepatocytes was reduced with increasing doses of CMTTD and especially BCMTD. The acid 1-mono(carboxyethylthio)tetradecane (CETTD), which is able to undergo one cycle of beta-oxidation, caused no change in liver weight, and only marginal effects on peroxisomes and mitochondria were observed. In contrast to the BCMTD and CMTTD feeding, the animals developed a tremendous accumulation of fat in the livers: the volume fraction of lipid droplets increased 23-fold after CETTD feeding.

MeSH terms

  • Animals
  • Carnitine O-Palmitoyltransferase / metabolism
  • Dicarboxylic Acids / metabolism*
  • Liver / cytology*
  • Liver / metabolism
  • Male
  • Microbodies / metabolism
  • Microbodies / ultrastructure*
  • Microscopy, Electron
  • Mitochondria, Liver / enzymology
  • Mitochondria, Liver / metabolism
  • Mitochondria, Liver / ultrastructure*
  • Oxidation-Reduction
  • Propionates / metabolism
  • Rats
  • Rats, Inbred Strains
  • Sulfides / metabolism*

Substances

  • Dicarboxylic Acids
  • Propionates
  • Sulfides
  • 1-(carboxyethylthio)tetradecane
  • 1,10-bis(carboxymethylthiodecane)
  • 1-(carboxymethylthio)tetradecane
  • Carnitine O-Palmitoyltransferase