J Surg Res. 2020 Jan 31;250:23-38. doi: 10.1016/j.jss.2019.12.025. [Epub ahead of print] https://www.ncbi.nlm.nih.gov/pubmed/32014698
Heterogeneous Response in Rabbit Fetal Diaphragmatic Hernia Lungs After Tracheal Occlusion.
Dobrinskikh E1, Al-Juboori SI2, Oria M3, Reisz JA4, Zheng C4, Peiro JL3, Marwan AI5.
Author information
Abstract
BACKGROUND:
Fetal tracheal occlusion (TO) is an experimental therapeutic approach to stimulate lung growth in the most severe congenital diaphragmatic hernia (CDH) cases. We have previously demonstrated a heterogeneous response of normal fetal rabbit lungs after TO with the appearance of at least two distinct zones. The aim of this study was to examine the fetal lung response after TO in a left CDH fetal rabbit model.
METHODS:
Fetal rabbits at 25 d gestation underwent surgical creation of CDH followed by TO at 27 d and harvest on day 30. Morphometric analysis, global metabolomics, and fluorescence lifetime imaging microscopy (FLIM) were performed to evaluate structural and metabolic changes in control, CDH, and CDH + TO lungs.
RESULTS:
Right and left lungs were different at the baseline and had a heterogeneous pulmonary growth response in CDH and after TO. The relative percent growth of the right lungs in CDH + TO was higher than the left lungs. Morphometric analyses revealed heterogeneous tissue-to-airspace ratios, in addition to size and number of airspaces within and between the lungs in the different groups. Global metabolomics demonstrated a slower rate of metabolism in the CDH group with the left lungs being less metabolically active. TO stimulated metabolic activity in both lungs to different degrees. FLIM analysis demonstrated local heterogeneity in glycolysis, oxidative phosphorylation (OXPHOS), and FLIM “lipid-surfactant” signal within and between the right and left lungs in all groups.
CONCLUSIONS:
We demonstrate that TO leads to a heterogeneous morphologic and metabolic response within and between the right and left lungs in a left CDH rabbit model.
Copyright © 2020 Elsevier Inc. All rights reserved.
KEYWORDS:
Congenital diaphragmatic hernia; Fluorescence lifetime imaging microscopy; Metabolic landscape; Parenchymal morphology; Pulmonary hypoplasia; Tracheal occlusionPMID: 32014698 DOI: 10.1016/j.jss.2019.12.025
