Premium
Synthesis of linoleate and α‐linolenate by chain elongation in the rat
Author(s) -
Cunnane Stephen C.,
Ryan Mary Ann,
Craig Kerr S.,
Brookes Steven,
Koletzko Berthold,
Demmelmair Hans,
Singer Janet,
Kyle David J.
Publication year - 1995
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/bf02537807
Subject(s) - linolenate , lipidology , chemistry , clinical chemistry , biochemistry , food science , phospholipid , fatty acid , membrane
The objective was to determine whether rats could synthesize longer chain polyunsaturates from hexadecadienoate (16∶2n−6) and hexadecatrienoate (16∶3n−3). Rats were gavaged with uniformly 13 C‐labelled hexadecadienoate or hexadecatrienoate, euthanized 24 h later, and total lipids were extracted from liver and carcass. Gas chromatogrpahy/combustion/isotope ratio mass spectrometry was used to measure 13 C levels in individual liver, carcass, and whole body fatty acids. 13 C Enrichment was present in desaturated and chain‐elongated polyunsaturates, including linoleate, arachidonate, α‐linolenate, and docosahexaenoate at 12–13% of the dose of tracer given. 13 C Enrichment from hexadecatrienoate was highest in carcass and liver α‐linolenate, representing 3.5 and 17.9% of the total α‐linolenate pool, respectively. For linoleate, arachidonate, or docosahexaenoate, the contribution of 13 C did not exceed 0.2% of the total body pool. Green leafy vegetables common in the human diet were shown to contain up to 1.2% of total fatty acids as hexadecadienoate and 11.6% as hexadecatrienoate. Hence, humans consuming green vegetables probably synthesize a small proportion of their total body content of linoleate and α‐linolenate.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom