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Intermediates in endogenous synthesis of C22:6 omega 3 and C20:4 omega 6 by term and preterm infants

Sauerwald TU, Hachey DL, Jensen CL, Chen H, Anderson RE, Heird WC

Pediatric research · 95 citas

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Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Solo mecanismos

Quién lo pagó

Financiación
Financiación independiente
Gobierno
National Eye Institute
Gobierno
NEI NIH HHS
Subvenciones
National Eye Institute (EY04149); National Eye Institute (EY 00871)

Según 2 financiadores declarados.

Publicación

Publicado
1997-02-01 · Pediatr Res · vol. 41 · número 2 · págs. 183–187
Editorial
Springer Nature
Citado
149 citas · más que el 99% de estudios similares · 10.6× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
20 trabajos
Acceso
De pago
Áreas de investigación
Fatty Acid Research and Health · Lipid metabolism and biosynthesis · Aquaculture Nutrition and Growth
Palabras clave
preterm infants, term infants, isotopic labeling, plasma phospholipids, fatty acid elongation, fatty acid desaturation, fatty acid beta-oxidation
MeSH
humans, docosahexaenoic acids, fatty acids, arachidonic acid, phospholipids, gestational age, infant, newborn, infant, premature

6 autores

  • Thorsten U. Sauerwald🇺🇸Agricultural Research Service; Children's Nutrition Research Center at Baylor College of Medicine
  • David L. Hachey🇺🇸Baylor College of Medicine; Children's Nutrition Research Center at Baylor College of Medicine
  • Craig L. Jensen🇺🇸Baylor College of Medicine; Children's Nutrition Research Center at Baylor College of Medicine
  • Huiming Chen🇺🇸Baylor College of Medicine
  • Robert E. Anderson🇺🇸Baylor College of Medicine
  • William C. Heird🇺🇸Baylor College of Medicine; Children's Nutrition Research Center at Baylor College of Medicine

Resumen

El texto original del estudio, en el idioma en que se publicó.

An alternative pathway of omega 3 and omega 6 fatty acid metabolism has been described in isolated rate hepatocytes and human fibroblasts. This alternative pathway, which is independent of delta 4 desaturation, involves elongation of C22 5 omega 3 and C22:4 omega 6 to C24 fatty acids, delta 6 desaturation of the C24 fatty acids and subsequent beta oxidation of the desaturated products to C22:6 omega 3 and C22:5 omega 6. To determine whether this alternative pathway is operative in the human infant and also to obtain additional information concerning endogenous conversion of C18:3 omega 3 and C18:2 omega 6 to longer chain more unsaturated fatty acids, presence of [M + 18] isotopomers of omega 3 and omega 6 fatty acids in the plasma phospholipid fraction of term and preterm infants after administration of [U-13C]18:3 omega 3 and [U-13C]18:2 omega 6 was determined by negative chemical ionization gas chromatography/mass spectrometry. [M + 18] isotopomers of the following omega 3 fatty acids were detected: C18:3, C18:4, C20:3, C20:4, C20:5, C22:4, C22:5, C22:6, C24:4 (two infants only), C24:5, and C24:6. [M + 18] isotopomers of omega 6 fatty acids detected included only C18:2, C18:3, C20:2, C20:3, and C20:4, but sensitivity was insufficient to detect [M + 18] isotopomers of C22 and C24 omega 6 fatty acids. Presence of [M + 18] isotopomers of C24:5 omega 3 and C24:6 omega 3 indicates that these fatty acids were synthesized endogenously from C18:3 omega 3. This plus the in vitro data strongly suggests that infants use the recently described alternative pathway in endogenous synthesis of C22:6 omega 3. However, involvement also of delta 4 desaturation cannot be excluded. Detection of [M + 18] isotopomers of C20:3 omega 3, C20:2 omega 6, and C22:4 omega 3 suggests that C18:3 omega 3, C18:2 omega 6, and C20:4 omega 3 are elongated as well as desaturated. The specific fate of these elongation products and their importance in endogenous synthesis of omega 3 and omega 6 long chain polyunsaturated fatty acids remain to be determined.

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