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Synthesis of linoleate and α-linolenate by chain elongation in the rat

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Lipids

Abstract

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 uniformly13C-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 measure13C levels in individual liver, carcass, and whole body fatty acids.13C 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.13C 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 of13C 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.

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Abbreviations

GC/C/IRMS:

gas chromatography/combustion/isotope ratio mass spectrometry

PUFA:

polyunsaturate fatty acids

References

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Cunnane, S.C., Ryan, M.A., Craig, K.S. et al. Synthesis of linoleate and α-linolenate by chain elongation in the rat. Lipids 30, 781–783 (1995). https://doi.org/10.1007/BF02537807

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  • DOI: https://doi.org/10.1007/BF02537807

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