Surfactant phospholipid kinetics in ventilated children after therapeutic surfactant supplementation
Surfactant phospholipid kinetics in ventilated children after therapeutic surfactant supplementation
Acute lung Injury leads to alterations in surfactant lipid composition and metabolism. Although several mechanisms contribute to dysregulated surfactant metabolism, studies investigating in vivo surfactant metabolism are limited. The aim of this study is to characterise surfactant phospholipid composition and flux utilising a stable isotope labelling technique in mechanically ventilated paediatric patients. Paediatric patients (<16 years of age) received 3.6 mg/kg intravenous methyl-D 9-choline chloride followed by the endotracheal instillation of 100 mg/kg of exogenous surfactant after 24 h. Bronchioalveolar fluid samples were taken at baseline and 12, 24, 36, 48, 72 and 96 h after methyl-D 9-choline infusion. Nine participants (median age of 48 days) were recruited. The primary phosphatidylcholine (PC) composition consisted of PC16:0/16:0 or DPPC (32.0 ± 4.5%). Surfactant supplementation resulted in a 30% increase in DPPC. Methyl-D 9 PC enrichment was detected after 12 h and differed significantly between patients, suggesting variability in surfactant synthesis/secretion by the CDP-choline pathway. Peak enrichment was achieved (0.94 ± 0.15% of total PC) at 24 h after methyl-D 9-choline infusion. There was a trend towards reduced enrichment with the duration of mechanical ventilation prior to study recruitment; however, this was not statistically significant (p = 0.19). In this study, we demonstrated the fractional molecular composition and turnover of surfactant phospholipids, which was highly variable between patients.
intensive care, paediatric, phospholipids, surfactant, ventilation
Goss, Victoria M.
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Dushianthan, Ahilanandan
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McCorkell, Jenni
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Morton, Katy
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Goss, Kevin C.W.
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Marsh, Michael J.
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Pappachan, John V.
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Postle, Anthony D.
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29 September 2024
Goss, Victoria M.
ef02be5d-9318-4f7d-b076-3153555980d0
Dushianthan, Ahilanandan
013692a2-cf26-4278-80bd-9d8fcdb17751
McCorkell, Jenni
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Morton, Katy
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Goss, Kevin C.W.
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Marsh, Michael J.
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Pappachan, John V.
8e1bd6bd-1cb9-4dd9-a9af-b9eed5459148
Postle, Anthony D.
0fa17988-b4a0-4cdc-819a-9ae15c5dad66
Goss, Victoria M., Dushianthan, Ahilanandan, McCorkell, Jenni, Morton, Katy, Goss, Kevin C.W., Marsh, Michael J., Pappachan, John V. and Postle, Anthony D.
(2024)
Surfactant phospholipid kinetics in ventilated children after therapeutic surfactant supplementation.
International Journal of Molecular Sciences, 25 (19), [10480].
(doi:10.3390/ijms251910480).
Abstract
Acute lung Injury leads to alterations in surfactant lipid composition and metabolism. Although several mechanisms contribute to dysregulated surfactant metabolism, studies investigating in vivo surfactant metabolism are limited. The aim of this study is to characterise surfactant phospholipid composition and flux utilising a stable isotope labelling technique in mechanically ventilated paediatric patients. Paediatric patients (<16 years of age) received 3.6 mg/kg intravenous methyl-D 9-choline chloride followed by the endotracheal instillation of 100 mg/kg of exogenous surfactant after 24 h. Bronchioalveolar fluid samples were taken at baseline and 12, 24, 36, 48, 72 and 96 h after methyl-D 9-choline infusion. Nine participants (median age of 48 days) were recruited. The primary phosphatidylcholine (PC) composition consisted of PC16:0/16:0 or DPPC (32.0 ± 4.5%). Surfactant supplementation resulted in a 30% increase in DPPC. Methyl-D 9 PC enrichment was detected after 12 h and differed significantly between patients, suggesting variability in surfactant synthesis/secretion by the CDP-choline pathway. Peak enrichment was achieved (0.94 ± 0.15% of total PC) at 24 h after methyl-D 9-choline infusion. There was a trend towards reduced enrichment with the duration of mechanical ventilation prior to study recruitment; however, this was not statistically significant (p = 0.19). In this study, we demonstrated the fractional molecular composition and turnover of surfactant phospholipids, which was highly variable between patients.
Text
ijms-25-10480
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Accepted/In Press date: 27 September 2024
Published date: 29 September 2024
Keywords:
intensive care, paediatric, phospholipids, surfactant, ventilation
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Local EPrints ID: 495402
URI: http://eprints.soton.ac.uk/id/eprint/495402
ISSN: 1422-0067
PURE UUID: ac3255e8-3f4f-49c4-a9c5-7daaef35b374
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Date deposited: 12 Nov 2024 18:12
Last modified: 13 Nov 2024 02:56
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Author:
Victoria M. Goss
Author:
Ahilanandan Dushianthan
Author:
Jenni McCorkell
Author:
Katy Morton
Author:
Kevin C.W. Goss
Author:
Michael J. Marsh
Author:
John V. Pappachan
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