The Journal of Pediatrics
Volume 147, Issue 4 , Pages 480-485, October 2005

Substrate utilization and kinetics of surfactant metabolism in evolving bronchopulmonary dysplasia

From the Division of Newborn Medicine, the Edward Mallinckrodt Department of Pediatrics, Washington University School of Medicine, and St. Louis Children's Hospital, St Louis, Missouri; and the Division of Geriatrics and Nutritional Science, Department of Internal Medicine, Washington University School of Medicine, St Louis, Missouri

Received 11 January 2005; received in revised form 1 April 2005; accepted 15 April 2005.

Objectives

To use stable isotopically labeled precursors of pulmonary surfactant phospholipids to measure precursor utilization and surfactant turnover in premature infants who required mechanical ventilation at birth, 2 weeks, and >4 weeks of age.

Study design

Infants of ≤28 weeks' gestation received simultaneous 24-hour intravenous infusions of [1,2,3,4-13C4] palmitate and [1-13C1] acetate at birth, 2 weeks, and ≥4 weeks of life. Disaturated phospholipids were extracted from sequential tracheal aspirate samples obtained over a period of 2 weeks. Fractional catabolic rate (a measure of total turnover) and the fractional synthetic rates from plasma palmitate and de novo synthesis (acetate) were measured.

Results

The fractional catabolic rate increased from 25.3% ± 7.0% per day at birth to 53.8% ± 14.4% per day at 4 weeks (P=.001). The combined contribution from plasma palmitate and de novo synthesis to total synthesis increased from 44.2% ± 19.8% at birth to 85.2% ± 32.8% at 4 weeks (P=.03).

Conclusions

Total surfactant turnover increased in premature infants with evolving bronchopulmonary dysplasia. The increasing contributions from acetate and plasma palmitate suggest a decrease in surfactant phospholipid recycling.

BPD, Bronchopulmonary dysplasia, FSR, Fractional synthetic rate, FCR, Fractional catabolic rate, DSPC, Disaturated phosphatidylcholine, DSPL, Disaturated phospholipid, GC/MS, Gas chromatography/mass spectrometry, TTR, Tracer to tracee ratio

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 Supported by grants from F32-HLO74601 (K.S.), Forest Pharmaceuticals Fellow Grants (K.S., J.Z.), NIH DK56341 (Clinical Nutrition Research Unit), NIH RR00954 (Biomedical Mass Spectrometry Resource), and NIH HL65385 (A.H.).

PII: S0022-3476(05)00348-3

doi:10.1016/j.jpeds.2005.04.039

The Journal of Pediatrics
Volume 147, Issue 4 , Pages 480-485, October 2005