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Concentration dependence of a poly-leucine surfactant protein C analogue on in vitro and in vivo surfactant activity

  • Jan Johansson
  • , Tore Curstedt
  • , Bengt Robertson
  • , A Almlén

    Publication: Contribution to journalJournal article

    Abstract

    Background: Modified natural surfactants currently used for treatment of respiratory distress syndrome contain about 0.5 -1% (w/w phospholipids) of each of the surfactant proteins SP-B and SP-C. The supply of these preparations is limited and synthetic surfactant preparations containing lipids and peptides are under development. Objectives: To investigate the potential of different concentrations of the SP-C analogue SP-C33 in 1,2-dipalmitoyl-sn -glycero-3-phosphocholine/ 1-palmitoyl-2-oleoyl-sn -glycero-3-phosphoglycerol (68: 31, w/w). Methods: Surface activity was evaluated in pulsating and captive bubble surfactometers and in immature newborn rabbits. Results: Preparations containing 6 1% SP-C33 achieve minimum surface tension ! 5 mN/m indicating good biophysical activity, and increase tidal volumes in premature rabbit fetuses to the same level as a modified natural surfactant preparation does. Alveolar patency at end expiration, as evaluated by measurement of lung gas volumes, histological assessment of alveolar expansion and determination of alveolar volume density, was lower in the animals treated with synthetic surfactant than in those receiving modified natural surfactant. Conclusions: These data suggest that SP- C33 is similarly efficient as the native peptide in improving surface properties of phospholipids mixtures and in increasing lung compliance in surfactant-deficient states, but that other components are needed to maintain alveolar stability at low airway pressures. Copyright (C) 2007 S. Karger AG, Basel.
    Original languageEnglish
    Pages (from-to)194-200
    Number of pages7
    JournalNeonatology
    Volume92
    Issue number3
    DOIs
    Publication statusPublished - 2007

    Keywords

    • pulmonary surfactant
    • neonatal respiratory distress syndrome
    • membrane protein
    • synthetic peptide

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