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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1991-2-1
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pubmed:abstractText |
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.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1,10-bis(carboxymethylthiodecane),
http://linkedlifedata.com/resource/pubmed/chemical/1-(carboxyethylthio)tetradecane,
http://linkedlifedata.com/resource/pubmed/chemical/1-(carboxymethylthio)tetradecane,
http://linkedlifedata.com/resource/pubmed/chemical/Carnitine O-Palmitoyltransferase,
http://linkedlifedata.com/resource/pubmed/chemical/Dicarboxylic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Propionic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfides
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1047-8477
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
103
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
257-65
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:2261310-Animals,
pubmed-meshheading:2261310-Carnitine O-Palmitoyltransferase,
pubmed-meshheading:2261310-Dicarboxylic Acids,
pubmed-meshheading:2261310-Liver,
pubmed-meshheading:2261310-Male,
pubmed-meshheading:2261310-Microbodies,
pubmed-meshheading:2261310-Microscopy, Electron,
pubmed-meshheading:2261310-Mitochondria, Liver,
pubmed-meshheading:2261310-Oxidation-Reduction,
pubmed-meshheading:2261310-Propionic Acids,
pubmed-meshheading:2261310-Rats,
pubmed-meshheading:2261310-Rats, Inbred Strains,
pubmed-meshheading:2261310-Sulfides
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pubmed:year |
1990
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pubmed:articleTitle |
Morphologic effects of sulfur-substituted fatty acids on rat hepatocytes with special reference to proliferation of peroxisomes and mitochondria.
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pubmed:affiliation |
Zoological Laboratory, University of Bergen, Norway.
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pubmed:publicationType |
Journal Article
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