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Experimental inhibition of peroxisomal β-oxidation in rats: Influence on brain myelination

✍ Scribed by Christiane Van Den Branden; Jan Leeman; Georges Dacremont; Robert Collumbien; Frank Roels


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
598 KB
Volume
3
Category
Article
ISSN
0894-1491

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✦ Synopsis


Oral administration of thioridazine, an inhibitor of perox tsomal p-oxidation, to normal rats from weaning till day 60 causes a small increase of the very long chain fatty acid C26 in brain lipids. Myelination in the brain is decreased. In the genu of the corpus callosum the ratio of non-myelinatedmyelinated axons is increased. In the commissura anterior the myelin sheaths of the axons are significantly thinner in treated than in control animals. Undernourishment caused by the drug is minimal in this experiment. Area and total DNA of glial nuclei are unaltered in both the genu and the commissura anterior of treated rats. The distribution of chromatin (texture), however, shows small differences in the corpus callosum.


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Inhibition of peroxisomal beta-oxidation
✍ Christiane Van Den Branden; Georges Dacremont; Robert Hooghe; Frank Roels 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 English ⚖ 608 KB

Thioridazine, an inhibitor of peroxisomal beta-oxidation, was administered orally to nursing rats during the period of maximal myelination in the pups (8-21 days postnatally). Under the experimental conditions, thioridazine causes accumulation of C24 and C26 fatty acids in pup brain lipids, an effec