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Morphological alterations of exogenous surfactant inhibited by meconium can be prevented by dextran

BACKGROUND: Surfactant dysfunction due to inhibition is involved in the pathophysiology of meconium aspiration syndrome. Dextran addition has been shown to reverse exogenous surfactant inactivation by meconium, but the precise mechanisms and the morphological correlate of this effect are yet unknown...

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Autores principales: Ochs, Matthias, Schüttler, Markus, Stichtenoth, Guido, Herting, Egbert
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1489943/
https://www.ncbi.nlm.nih.gov/pubmed/16756655
http://dx.doi.org/10.1186/1465-9921-7-86
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author Ochs, Matthias
Schüttler, Markus
Stichtenoth, Guido
Herting, Egbert
author_facet Ochs, Matthias
Schüttler, Markus
Stichtenoth, Guido
Herting, Egbert
author_sort Ochs, Matthias
collection PubMed
description BACKGROUND: Surfactant dysfunction due to inhibition is involved in the pathophysiology of meconium aspiration syndrome. Dextran addition has been shown to reverse exogenous surfactant inactivation by meconium, but the precise mechanisms and the morphological correlate of this effect are yet unknown. Morphological surfactant analysis by transmission electron microscopy (TEM) and stereology allows the differentiation of active (large aggregates = LA) and inactive (small aggregates = SA) subtypes. METHODS: To determine the in vitro effects of meconium and dextran addition on the morphology of a modified porcine natural surfactant (Curosurf), Curosurf samples were either incubated alone or together with meconium or with meconium and dextran, fixed and processed for TEM. Volume fractions of surfactant subtypes [lamellar body-like forms (LBL), multilamellar vesicles (MV), unilamellar vesicles (UV)] were determined stereologically. RESULTS: All preparations contained LBL and MV (corresponding to LA) as well as UV (corresponding to SA). The volume fraction of UV increased with addition of meconium and decreased with further addition of dextran. Correspondingly, the UV/(LBL+MV) ratio (resembling the SA/LA ratio) increased when meconium was added and decreased when dextran was added to the surfactant-meconium mixture. CONCLUSION: Meconium causes alterations in the ultrastructural composition of Curosurf that can be visualized and analyzed by TEM and stereology. These alterations resemble an increase in the SA/LA ratio and are paralleled by an increase in minimum surface tension. Dextran prevents these effects and may therefore be a useful additive to exogenous surfactant preparations to preserve their structural and functional integrity, thereby improving their resistance to inactivation.
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spelling pubmed-14899432006-07-08 Morphological alterations of exogenous surfactant inhibited by meconium can be prevented by dextran Ochs, Matthias Schüttler, Markus Stichtenoth, Guido Herting, Egbert Respir Res Research BACKGROUND: Surfactant dysfunction due to inhibition is involved in the pathophysiology of meconium aspiration syndrome. Dextran addition has been shown to reverse exogenous surfactant inactivation by meconium, but the precise mechanisms and the morphological correlate of this effect are yet unknown. Morphological surfactant analysis by transmission electron microscopy (TEM) and stereology allows the differentiation of active (large aggregates = LA) and inactive (small aggregates = SA) subtypes. METHODS: To determine the in vitro effects of meconium and dextran addition on the morphology of a modified porcine natural surfactant (Curosurf), Curosurf samples were either incubated alone or together with meconium or with meconium and dextran, fixed and processed for TEM. Volume fractions of surfactant subtypes [lamellar body-like forms (LBL), multilamellar vesicles (MV), unilamellar vesicles (UV)] were determined stereologically. RESULTS: All preparations contained LBL and MV (corresponding to LA) as well as UV (corresponding to SA). The volume fraction of UV increased with addition of meconium and decreased with further addition of dextran. Correspondingly, the UV/(LBL+MV) ratio (resembling the SA/LA ratio) increased when meconium was added and decreased when dextran was added to the surfactant-meconium mixture. CONCLUSION: Meconium causes alterations in the ultrastructural composition of Curosurf that can be visualized and analyzed by TEM and stereology. These alterations resemble an increase in the SA/LA ratio and are paralleled by an increase in minimum surface tension. Dextran prevents these effects and may therefore be a useful additive to exogenous surfactant preparations to preserve their structural and functional integrity, thereby improving their resistance to inactivation. BioMed Central 2006 2006-06-06 /pmc/articles/PMC1489943/ /pubmed/16756655 http://dx.doi.org/10.1186/1465-9921-7-86 Text en Copyright © 2006 Ochs et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Ochs, Matthias
Schüttler, Markus
Stichtenoth, Guido
Herting, Egbert
Morphological alterations of exogenous surfactant inhibited by meconium can be prevented by dextran
title Morphological alterations of exogenous surfactant inhibited by meconium can be prevented by dextran
title_full Morphological alterations of exogenous surfactant inhibited by meconium can be prevented by dextran
title_fullStr Morphological alterations of exogenous surfactant inhibited by meconium can be prevented by dextran
title_full_unstemmed Morphological alterations of exogenous surfactant inhibited by meconium can be prevented by dextran
title_short Morphological alterations of exogenous surfactant inhibited by meconium can be prevented by dextran
title_sort morphological alterations of exogenous surfactant inhibited by meconium can be prevented by dextran
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1489943/
https://www.ncbi.nlm.nih.gov/pubmed/16756655
http://dx.doi.org/10.1186/1465-9921-7-86
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