Surfactant-associated protein B kinetics in vivo in newborn infants by stable isotopes

被引:16
作者
Cogo, P
Baritussio, A
Rosso, F
Gucciardi, A
Moretti, V
Badon, T
Duner, E
Zimmernann, L
Carnielli, VP
机构
[1] Univ Padua, Dept Pediat, I-35128 Padua, Italy
[2] Univ Padua, Clin Med 1, Dept Med & Surg Sci, I-35128 Padua, Italy
[3] Salesi Children Hosp, Ancona, Italy
[4] Maasticht Univ, Dept Pediat, NL-6202 AZ Maastricht, Netherlands
[5] Salesi Children Hosp, Ancona, Italy
关键词
D O I
10.1203/01.PDR.0000155755.27716.04
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Surfactant-associated protein B (SP-B) is critical to the biophysical function of pulmonary surfactant. No information is available on SP-B synthesis and kinetics in humans. We administered a 24-h i.v. infusion of C-13-valine as metabolic precursor of SP-B to six newborn infants (weight 3.5 +/- 0.5 kg; age 12 d, range 1-43 d). Three of the study infants also received i.v. H-2-palmitate to label surfactant disaturated phosphatidylcholine (DSPC). SP-B and DSPC were isolated from tracheal aspirates, and their respective C-13 and H-2 enrichments were measured by gas chromatography-mass spectrometry. SP-B kinetics was measured successfully in all six infants. SP-B median (range) fractional synthesis rate was 30% per day (20-78% per day), secretion time was 4.5 h (1-9 h), time to peak was 24 h (12-36 h), and half-life was 21 h (8-35 h). The ascending part of the SP-B kinetic curve was similar to the DSPC curve, suggesting similar secretion pathways. SP-B half-life seemed to be shorter than DSPC half-life. These results agree with existing animal data. We conclude that the measurement of SP-B kinetics is feasible in vivo in humans by stable isotope technology.
引用
收藏
页码:519 / 522
页数:4
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