## Abstract The existence of a regulating site of the cholesterol synthetic pathway in rat liver located after the squalene formation is shown by a comparison of the incorporation of labelled acetate and mevalonate __in vivo__ over a period from 7.5 minutes to several hours under fasting and non fa
On Metabolic Degradations of Squalene, Lanosterol and Cholesterol in Rat Liver in vivo. Evidence for Recycling of Metabolites for the Synthesis of Isoprene Compounds
โ Scribed by Oswald; Verena Wiss
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- German
- Weight
- 412 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0018-019X
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โฆ Synopsis
Abstract
(1) Radioactivity of biosynthetically labeled squalene, injected in tracer amounts in rats is incorporated to about equal parts into cholesterol and component(s) of the fatty acid fraction of the liver. The ubiquinones isolated from the liver are radioactive and show about the same specific radioactivity as the cholesterol. It appears therefore, that the squalene which escapes incorporation into cholesterol is degraded to metabolite(s) suited for the synthesis of isoprene compounds.
(2) Radioactivity of injected biosynthetically and chemically labeled cholesterol is traced in the ubiquinones and the squalene of rat liver indicating that a degradation of cholesterol and a recycling of the metabolite(s) occurs.
(3) A recycling of metabolite(s) of squalene and of cholesterol can explain the observation that after labeled mevalonate or acetate as precursor, radioactivity can be traced in the squalene of the liver many hours after the injection and maintains a constant value during a period of several hours.
(4) Radioactivity of biosynthetically labeled lanosterol is not only incorporated into cholesterol but a considerable part of it into component(s) of the bile acid fraction of the liver. Evidence is obtained that this transformation occurs by circumventing cholesterol as intermediate.
๐ SIMILAR VOLUMES
## Abstract Physiological doses of insulin and glucagon in the range of 0.5โ2.5 m unit and 0.05โ2 ฮผg respectively per 100 g body weight stimulate first and inhibit afterwards the cholesterol synthesis from labeled acetate in rat liver __in vivo__. It could be shown that these effects are not caused