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Compartmental analyses of 2H5-a-linolenic acid and C-U-eicosapentaenoic acid toward synthesis of plasma labeled 22:6n-3 in newborn term infants
Oleh:
Yu, Hong Lin
;
Llanos, Adolfo
;
Mena, Patricia
;
Uauy, Ricardo
;
Salem, Norman (Jr.)
;
Pawlosky, Robert J.
Jenis:
Article from Journal - ilmiah internasional
Dalam koleksi:
The American Journal of Clinical Nutrition vol. 92 no. 02 (Aug. 2010)
,
page 284-293.
Topik:
Lipids
;
eicosapentaenoic acid (EPA)
;
docosahexaenoic acid (DHA)
Ketersediaan
Perpustakaan FK
Nomor Panggil:
A07.K.2010.02
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Background: During early postnatal development, the nervous system accretes docosahexaenoic acid (DHA; 22:6n-3), a highly unsaturated n-3 (omega-3) fatty acid (FA) used in the formation of neural cell membranes. DHA, which is present in human breast milk, may also be biosynthesized from n-3 FAs such as 18:3n-3 [a-linolenic acid (ALA)] or 20:5n-3 [eicosapentaenoic acid (EPA)]. An important concern is to what extent these precursors can supply DHA to the developing infant. Objective: We analyzed measurements of fractional percentages of plasma 2H5-ALA and 13C-U-EPA directed toward the synthesis of labeled 22:6n-3 in 11 newborn infants by using compartmental modeling procedures. Design: One-week-old infants received doses of 2H5-ALA and 13C-U-EPA ethyl esters enterally. We drew blood from the infants periodically and analyzed the plasma for endogenous and labeled n-3 FAs. From the time-course concentrations of the labeled FAs, we determined rate constant coefficients, fractional synthetic rates, and plasma turnover rates of n-3 FAs. Results: In infants, ˜0.04% of the 2H5-ALA dose converted to plasma 2H5-EPA. Plasma 2H5-EPA and 2H5-22:5n-3 [docosapentaenoic acid (DPA)] efficiently converted to 2H5-DPA and 2H5-DHA, respectively. The percentage of plasma 13C-U-EPA directed toward the synthesis of 13C-DHA was lower than the percentage of plasma 2H5-EPA that originated from 2H5-ALA. Conclusions: Endogenously synthesized EPA was efficiently converted to DHA. In comparison, preformed EPA was less efficiently used for DHA biosynthesis, which suggests a differential metabolism of endogenous EPA compared with exogenous EPA. However, on a per mole basis, preformed EPA was 3.6 times more effective toward DHA synthesis than was ALA. Newborns required an intake of ˜5 mg preformed DHA · kg-1 · d-1 to maintain plasma DHA homeostasis.
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