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Use of stable isotope labeling technique and mass isotopomer distribution analysis of [ 13 C]palmitate isolated from surfactant disaturated phospholipids to study surfactant in vivo kinetics in a premature infant
Author(s) -
Merchak Assaad,
Patterson Bruce W.,
Yarasheski Kevin E.,
Hamvas Aaron
Publication year - 2000
Publication title -
journal of mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 1076-5174
DOI - 10.1002/1096-9888(200006)35:6<734::aid-jms2>3.0.co;2-h
Subject(s) - chemistry , pulmonary surfactant , chromatography , palmitic acid , isotope ratio mass spectrometry , in vivo , mass spectrometry , gas chromatography–mass spectrometry , respiratory distress , fatty acid , biochemistry , medicine , microbiology and biotechnology , anesthesia , biology
Pulmonary surfactant is a complex mixture of phospholipids and proteins which lowers surface tension and maintains alveolar expansion at end expiration. Developmental and genetic disruption of pulmonary surfactant metabolism leads to respiratory distress in newborns. Stable isotope labeling of metabolic precursors of disaturated phospholipids, the most abundant and specific component of pulmonary surfactant, permits the measurement of the kinetics of surfactant metabolism in vivo . We measured [U‐ 13 C 6 ]glucose incorporation into palmitic acid derived from disaturated surfactant phospholipids. A 24 h infusion of [U‐ 13 C 6 ]glucose (140 mg kg −1 ) was administered to a premature infant who required mechanical ventilation for respiratory distress syndrome; tracheal aspirate samples were obtained at the start of the infusion and at regular intervals for the next 70 h. Each tracheal aspirate sample was incubated with osmium tetroxide to isolate disaturated surfactant phospholipids. Methyl esters of the fatty acids in the disaturated phospholipids were prepared and the enrichment of [ 13 C]methyl palmitate was measured by gas chromatography/mass spectrometry (GC/MS) and gas chromatography/combination/isotope ratio mass spectrometry (GC/C/IRMS). Mass isotopomer distribution analysis (MIDA) was used to calculate the fractional synthetic rate (FSR) of palmitate synthesized from acetate. With both GC/MS and GC/C/IRMS, palmitate 13 C enrichment was first detected 12.3 h after the start of the tracer infusion. The enrichment increased in a linear fashion, reached a peak at 47 h and remained constant in the remainder of the samples. The FSR of palmitate from acetate was 5.2% per day. Stable isotope techniques and MIDA will provide insights into the kinetics of surfactant metabolism in newborns with respiratory dysfunction. Copyright © 2000 John Wiley & Sons, Ltd.