Literature DB >> 30856517

Heterogeneous Pulmonary Response After Tracheal Occlusion: Clues to Fetal Lung Growth.

Evgenia Dobrinskikh1, Saif I Al-Juboori2, Uladzimir Shabeka2, Julie A Reisz3, Connie Zheng3, Ahmed I Marwan4.   

Abstract

BACKGROUND: Understanding inconsistent clinical outcomes in infants with severe congenital diaphragmatic hernia (CDH) after tracheal occlusion (TO) is a crucial step for advancing neonatal care. The objective of this study is to explore the heterogeneous airspace morphometry and the metabolic landscape changes in fetal lungs after TO.
METHODS: Fetal lungs on days 1 and 4 after TO were examined using mass spectrometry-based metabolomics, fluorescence lifetime imaging microscopy (FLIM), the number of airspaces, and tissue-to-airspace ratio (TAR).
RESULTS: Two morphometric areas were identified in TO lungs compared with controls (more small airspaces at day 1 and a higher number of enlarged airspaces at day 4). Global metabolomics analysis revealed a significant upregulation of glycolysis and a suppression of the tricarboxylic acid cycle in day 4 TO lungs compared with day 1 TO lungs. In addition, there was a significant increase in polyamines involved in cell growth and proliferation. Locally, FLIM analysis on day 1 TO lungs demonstrated two types of heterogeneous zones-similar to control and with increased oxidative phosphorylation. FLIM on day 4 TO lungs demonstrated appearance of zones with enlarged airspaces and a metabolic shift toward glycolysis, accompanied by a decrease in the FLIM "lipid-surfactant" signal.
CONCLUSIONS: In normal fetal lungs, we report a novel temporal pattern of varied morphometric and metabolic changes. Initially, there is formation of zones with small airspaces, followed by airspace enlargement over time. Metabolically day 1 TO lungs have zones with increased oxidative phosphorylation, whereas day 4 TO lungs have a shift toward glycolysis in the enlarged airspaces. Based on our observations, we speculate that the "best responders" to tracheal occlusion should have bigger lungs with small airspaces and normal surfactant production.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Congenital diaphragmatic hernia; Fluorescence lifetime imaging microscopy; Heterogeneous metabolic zones; Metabolic landscape; Pulmonary hypoplasia; Tracheal occlusion

Mesh:

Substances:

Year:  2019        PMID: 30856517     DOI: 10.1016/j.jss.2019.02.015

Source DB:  PubMed          Journal:  J Surg Res        ISSN: 0022-4804            Impact factor:   2.192


  3 in total

1.  Maternal Pyrroloquinoline Quinone Supplementation Improves Offspring Liver Bioactive Lipid Profiles throughout the Lifespan and Protects against the Development of Adult NAFLD.

Authors:  Ashok Mandala; Evgenia Dobrinskikh; Rachel C Janssen; Oliver Fiehn; Angelo D'Alessandro; Jacob E Friedman; Karen R Jonscher
Journal:  Int J Mol Sci       Date:  2022-05-27       Impact factor: 6.208

2.  The developing murine lung is susceptible to acetaminophen toxicity.

Authors:  Evgenia Dobrinskikh; Laura G Sherlock; David J Orlicky; Lijun Zheng; Robyn De Dios; Durga Balasubramaniyan; Thom Sizemore; Brittany Butler; Clyde J Wright
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2021-03-24       Impact factor: 5.464

3.  Neuronal Lipoprotein Lipase Deficiency Alters Neuronal Function and Hepatic Metabolism.

Authors:  Kimberley D Bruce; Evgenia Dobrinskikh; Hong Wang; Ivan Rudenko; Hong Gao; Andrew E Libby; Sachi Gorkhali; Tian Yu; Andrea Zsombok; Robert H Eckel
Journal:  Metabolites       Date:  2020-09-28
  3 in total

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