Evidence map›Paper›PMID 33502935›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2021

A shift from glycolytic and fatty acid derivatives toward one-carbon metabolites in the developing lung during transitions of the early postnatal period.

Daniel D Lee, Sang Jun Park, Kirsten L Zborek, Margaret A Schwarz

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Cell Population-resolved Multiomics Atlas of the Developing Lung.American journal of respiratory cell and molecular biology · 2025
    Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Daniel D LeeDepartment of Pediatrics, Indiana University School of Medicine, Indiana University, Indianapolis, Indiana.
Sang Jun ParkDepartment of Preprofessional Studies, University of Notre Dame, South Bend, Indiana.
Kirsten L ZborekDepartment of Cellular and Integrative Physiology, Indiana University School of Medicine, Indiana University, Indianapolis, Indiana.
Margaret A SchwarzDepartment of Pediatrics, Indiana University School of Medicine, Indiana University, Indianapolis, Indiana.
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · USUniversity of Notre Dame · US

Funding

Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
IU Training Program in Molecular Physiology and Clinical Mechanisms of Lung DiseaseT32HL091816 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI Erick Forno, Roberto F. Machado · 2009 to 2026
$4.3M
Decoding Mediators in Lung DevelopmentR21HD090227 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI SCHWARZ, MARGARET A · 2018 to 2019
$433k
HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) 5R21HD090227-02HHS | NIH | National Center for Advancing Translational Sciences (NCATS) UL1TR001108HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) HL091816NCATS NIH HHS UL1 TR001108NHLBI NIH HHS T32 HL091816NICHD NIH HHS R21 HD090227
6 · The paper itself

Abstract

During postnatal lung development, metabolic changes that coincide with stages of alveolar formation are poorly understood. Responding to developmental and environmental factors, metabolic changes can be rapidly and adaptively altered. The objective of the present study was to determine biological and technical determinants of metabolic changes during postnatal lung development. Over 118 metabolic features were identified by liquid chromatography with tandem mass spectrometry (LC-MS/MS, Sciex QTRAP 5500 Triple Quadrupole). Biological determinants of metabolic changes were the transition from the postnatal saccular to alveolar stages and exposure to 85% hyperoxia, an environmental insult. Technical determinants of metabolic identification were brevity and temperature of harvesting, both of which improved metabolic preservation within samples. Multivariate statistical analyses revealed the transition between stages of lung development as the period of major metabolic alteration. Of three distinctive groups that clustered by age, the saccular stage was identified by its enrichment of both glycolytic and fatty acid derivatives. The critical transition between stages of development were denoted by changes in amino acid derivatives. Of the amino acid derivatives that significantly changed, a majority were linked to metabolites of the one-carbon metabolic pathway. The enrichment of one-carbon metabolites was independent of age and environmental insult. Temperature was also found to significantly influence the metabolic levels within the postmortem sampled lung, which underscored the importance of methodology. Collectively, these data support not only distinctive stages of metabolic change but also highlight amino acid metabolism, in particular one-carbon metabolites as metabolic signatures of the early postnatal lung.

Indexed as

GlycolysisMetabolomeAnimalsAnimals, NewbornCarbonChromatography, LiquidFatty AcidsLungMaleMetabolic Networks and PathwaysMiceMice, Inbred C57BLTandem Mass SpectrometryCarbonFatty Acidsalveologenesishyperoxialung maturation and developmentmetabolomicsone-carbon metabolism

Identifiers

PMID33502935
PMCPMC8238155
OpenAlexW3125750388

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.