Biosynthesis of polyunsaturated fatty acids in the developing brains. II. Metabolic transformations of intracranially administered (3-/sup 14/C) eicosatrienoic acid, evidence for lack of. delta. /sup 8/ desaturase
Journal Article
·
· Lipids; (United States)
OSTI ID:7230425
(3-/sup 14/C) Eicosatrienoic acid (..delta..11,14,17) chemically synthesized from (1-/sup 14/C) linolenic acid was injected intracranially into 14-day old rats and sacrificed 8 hr later. The analysis of brain fatty acids by radio-gas liquid chromatography before and after ozonolysis showed that the tetraene fraction consisted of a desaturated product, ..delta..5,11,17-20:4, and its elongated product, ..delta..7,13,16,19-22:4. Both of these products, with a combined total of 61% of the total radioactivity recovered in the tetraene fraction, contain a nonmethylene interrupted double bond system and, therefore, are unsuitable for further desaturation. The other two components, ..delta..6,9,12,15-18:4 and ..delta..8,11,14,17-20:4, must have been formed from ..delta..9,12,15-18:3, formed by retroconversion of the starting material 20:3, followed by desaturation and elongation. These results suggest a lack of ..delta../sup 8/ desaturase in the developing brain, leading to formation of ..delta..5,11,14,17-20:4 rather than ..delta..8,11,14,17-20:4. However, the nonmethylene interrupted double bond isomer does not restrict chain elongation.
- Research Organization:
- Univ. of California, Los Angeles
- OSTI ID:
- 7230425
- Journal Information:
- Lipids; (United States), Journal Name: Lipids; (United States) Vol. 11:9; ISSN LPDSA
- Country of Publication:
- United States
- Language:
- English
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