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Influence of dietary long-chain PUFA on premature baboon lung FA and dipalmitoyl PC composition
Authors:Angela?Chueh?Chao,Bassem?I.?Ziadeh,Guan-Yeu?Diau,Vasuki?Wijendran,Eszter?Sarkadi-Nagy,Andrea?T.?Hsieh,Peter?W.?Nathanielsz,J.?Thomas?Brenna  author-information"  >  author-information__contact u-icon-before"  >  mailto:jtb@cornell.edu."   title="  jtb@cornell.edu."   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Division of Nutritional Sciences, Cornell University, 14853 Ithaca, New York;(2) Present address: Division of Pediatric Surgery, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Ribapharm, 3300 Hyland Ave., Costa Mesa, CA 92626. Diau, 325 Chen Con Rd., Section 2, 10070 Nai-Whu, Taipei, Taiwan ROC;(3) Present address: Foster Biomedical Laboratory, MS029 Brandeis University, P.O. Box 549110, 02454 Waltham, MA;(4) Present address: Nutritional Sciences and Toxicology, University of California, Morgan Hall, 94720 Berkeley, CA;(5) Present address: New York University School of Medicine, Obstetrics and Gynecology, Women's Health Service, New York, NY
Abstract:One of the major survival challenges of premature birth is production of lung surfactant. The lipid component of surfactant, dipalmitoyl PC (DPPC), increases in concentration in the period before normal term birth via a net shift in FA composition away from unsaturates. We investigated the influence of dietary DHA and arachidonic acid (AA) on lung FA composition and DPPC concentration in term and preterm baboons. Pregnant animals/neonates were randomized to one of four groups: breast-fed (B), term formula-fed (T), preterm formulafed (P), and preterm fed formula supplemented with DHA-AA (P+). Breast milk contained 0.68%wt DHA and the P+ group formula contained 0.61%wt DHA. In the preterm groups (P and P+), pregnant females received a course of antenatal corticosteroids. At the adjusted age of 4 wk, neonate lung tissue was harvested, and FA composition and DPPC were analyzed. Palmitate was ∼28%wt of lung total FA and no significant differences were found among the four treatment groups. In contrast, DPPC in the B group lung tissue was significantly greater than DPPC in the unsupplemented groups, but not compared with the P+ group. The B and P+ groups were not significantly different in DHA and AA, but were different compared with the unsupplemented (T, P) groups. These results indicate that LCP supplementation increases lung DHA and AA, without compromising overall lung 16∶0 or DPPC. The shift in FA composition toward greater unsaturation in the groups consuming LCP supported improved surfactant lipid concentration in preterm neonate lungs.
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