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Surfactant phospholipid kinetics in ventilated children after therapeutic surfactant supplementation

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
1422-0067
Goss, Victoria M.
ef02be5d-9318-4f7d-b076-3153555980d0
Dushianthan, Ahilanandan
013692a2-cf26-4278-80bd-9d8fcdb17751
McCorkell, Jenni
b288c752-3bfd-4e30-9973-72e529252d23
Morton, Katy
164014a0-5b5c-46e8-89d8-8b1180f0ce58
Goss, Kevin C.W.
f81fb1f2-e427-459f-ba21-605eeda37640
Marsh, Michael J.
5c069300-5480-4be7-9046-8e6a21ba314f
Pappachan, John V.
8e1bd6bd-1cb9-4dd9-a9af-b9eed5459148
Postle, Anthony D.
0fa17988-b4a0-4cdc-819a-9ae15c5dad66
Goss, Victoria M.
ef02be5d-9318-4f7d-b076-3153555980d0
Dushianthan, Ahilanandan
013692a2-cf26-4278-80bd-9d8fcdb17751
McCorkell, Jenni
b288c752-3bfd-4e30-9973-72e529252d23
Morton, Katy
164014a0-5b5c-46e8-89d8-8b1180f0ce58
Goss, Kevin C.W.
f81fb1f2-e427-459f-ba21-605eeda37640
Marsh, Michael J.
5c069300-5480-4be7-9046-8e6a21ba314f
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).

Record type: Article

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.

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Accepted/In Press date: 27 September 2024
Published date: 29 September 2024
Keywords: intensive care, paediatric, phospholipids, surfactant, ventilation

Identifiers

Local EPrints ID: 495402
URI: http://eprints.soton.ac.uk/id/eprint/495402
ISSN: 1422-0067
PURE UUID: ac3255e8-3f4f-49c4-a9c5-7daaef35b374
ORCID for Ahilanandan Dushianthan: ORCID iD orcid.org/0000-0002-0165-3359
ORCID for Anthony D. Postle: ORCID iD orcid.org/0000-0001-7361-0756

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Date deposited: 12 Nov 2024 18:12
Last modified: 13 Nov 2024 02:56

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Contributors

Author: Victoria M. Goss
Author: Ahilanandan Dushianthan ORCID iD
Author: Jenni McCorkell
Author: Katy Morton
Author: Kevin C.W. Goss
Author: Michael J. Marsh
Author: John V. Pappachan

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