Evidence map›Paper›PMID 35269890›Full record

ArticleInternational journal of molecular sciences2022

Comprehensive Targeted Metabolomic Study in the Lung, Plasma, and Urine of PPE/LPS-Induced COPD Mice Model.

Hyeon-Young Kim, Hyeon-Seong Lee, In-Hyeon Kim, Youngbae Kim, Moongi Ji, Songjin Oh, Doo-Young Kim, Wonjae Lee, Sung-Hwan Kim, Man-Jeong Paik

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

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  12. Animal models and mechanisms of tobacco smoke-induced chronic obstructive pulmonary disease (COPD).Journal of toxicology and environmental health. Part B, Critical reviews · 2023
    Review
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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

10 authors at 6 institutions in 1 country.

Hyeon-Young KimJeonbuk Branch Institute, Korea Institute of Toxicology, Jeongeup 56212, Korea.
Hyeon-Seong LeeCollege of Pharmacy, Chosun University, Gwangju 61452, Korea.
In-Hyeon KimJeonbuk Branch Institute, Korea Institute of Toxicology, Jeongeup 56212, Korea.
Youngbae KimCollege of Pharmacy, Sunchon National University, Suncheon 57922, Korea.
Moongi JiCollege of Pharmacy, Sunchon National University, Suncheon 57922, Korea.
Songjin OhCollege of Pharmacy, Sunchon National University, Suncheon 57922, Korea.
Doo-Young KimCollege of Pharmacy, Sunchon National University, Suncheon 57922, Korea.
Wonjae LeeCollege of Pharmacy, Chosun University, Gwangju 61452, Korea.
Sung-Hwan KimJeonbuk Branch Institute, Korea Institute of Toxicology, Jeongeup 56212, Korea.
Man-Jeong PaikCollege of Pharmacy, Sunchon National University, Suncheon 57922, Korea.
Sunchon National University · KRKorea Institute of Toxicology · KRChonnam National University · KRChosun University · KRHyundai Pharm (South Korea) · KRKorea Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

(1) Background: Progression of chronic obstructive pulmonary disease (COPD) leads to irreversible lung damage and inflammatory responses; however, biomarker discovery for monitoring of COPD progression remains challenging. (2) Methods: This study evaluated the metabolic mechanisms and potential biomarkers of COPD through the integrated analysis and receiver operating characteristic (ROC) analysis of metabolic changes in lung, plasma, and urine, and changes in morphological characteristics and pulmonary function in a model of PPE/LPS-induced COPD exacerbation. (3) Results: Metabolic changes in the lungs were evaluated as metabolic reprogramming to counteract the changes caused by the onset of COPD. In plasma, several combinations of phenylalanine, 3-methylhistidine, and polyunsaturated fatty acids have been proposed as potential biomarkers; the α-aminobutyric acid/histidine ratio has also been reported, which is a novel candidate biomarker for COPD. In urine, a combination of succinic acid, isocitric acid, and pyruvic acid has been proposed as a potential biomarker. (4) Conclusions: This study proposed potential biomarkers in plasma and urine that reflect altered lung metabolism in COPD, concurrently with the evaluation of the COPD exacerbation model induced by PPE plus LPS administration. Therefore, understanding these integrative mechanisms provides new insights into the diagnosis, treatment, and severity assessment of COPD.

Indexed as

LipopolysaccharidesPulmonary Disease, Chronic ObstructiveAnimalsBiomarkersDisease Models, AnimalLungMicePersonal Protective EquipmentBiomarkersLipopolysaccharideschronic obstructive pulmonary diseasemetabolomicspotential biomarkerPPE/LPS-induced COPD exacerbation mice modelreceiver operating characteristic analysis

Identifiers

PMID35269890
PMCPMC8911395
OpenAlexW4214934969

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.