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Neonatal polyunsaturated fatty acid metabolism
Authors:Sheila M. Innis  Howard Sprecher  David Hachey  John Edmond  Robert E. Anderson
Affiliation:(1) Department of Paediatrics, University of British Columbia, V5Z 4H4 Vancouver, British Columbia, Canada;(2) Department of Medical Biochemistry, Ohio State University, 43210-1218 Columbus, Ohio;(3) Department of Pediatrics, Baylor College of Medicine, 77030 Houston, Texas;(4) Department of Biological Chemistry, University of California, 90095-1737 Los Angeles, California;(5) Departments of Ophthalmology and Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, 73104 Oklahoma City, Oklahoma;(6) B.C. Research Institute for Child and Family Health, 950 West 28th Ave., V5Z 4H4 Vancouver, B.C., Canada
Abstract:The importance of n−6 and n−3 polyunsaturated fatty acids (PUFA) in neonatal development, particularly with respect to the developing brain and retina, is well known. This review combines recent information from basic science and clinical studies to highlight recent advances in knowledge on PUFA metabolism and areas where research is still needed on infant n−6 and n−3 fatty acid requirements. Animal, cell culture, and infant studies are consistent in demonstrating that synthesis of 22∶6n−3 involves C24 PUFA and that the amounts of 18∶2n−6 and 18∶3n−3 influence PUFA metabolism. Studies to show that addition of n−6 fatty acids beyond Δ6-desaturase alters n−6 fatty acid metabolism with no marked increase in tissue 20∶4n−6 illustrate the limitations of analyses of tissue fatty acid compositions as an approach to study the effects of diet on fatty acid metabolism. New information to show highly selective pathways for n−6 and n−3 fatty acid uptake in brain, and efficient path-ways for conservation of 22∶6n−3 in retina emphasizes the differences in PUFA metabolism among different tissues and the unique features which allow the brain and retina to accumulate and maintain high concentrations of n−3 fatty acids. Further elucidation of the Δ6-desaturases involved in 24∶5n−6 and 22∶6n−3 synthesis; the regulation of fatty acid movement between the endoplasmic reticulum and peroxisomes; partitioning to acylation, desaturation and oxidation; and the effects of dietary and hormonal factors on these pathways is needed for greater understanding of neonatal PUFA metabolism.
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