Evidence map›Paper›PMID 36388083›Full record

ArticleDrug design, development and therapy2022

Integrated Microbiome and Metabolome Analysis Reveals Correlations Between Gut Microbiota Components and Metabolic Profiles in Mice with Methotrexate-Induced Hepatoxicity.

Changshui Wang, Shuzhen Zhao, Yuan Xu, Wenxue Sun, Yuanyuan Feng, Deshuai Liang, Yun Guan

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

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  18. Mechanism of the Effect of CompoundDrug design, development and therapy · 2023
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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

7 authors at 2 institutions in 1 country.

Changshui Wang *Department of Neurosurgery, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, 272000, People's Republic of China.
Shuzhen Zhao *Children's Rehabilitation Center, Jining Maternal and Child Health Family Planning Service Center, Jining, 272000, People's Republic of China.
Yuan XuDepartment of Hematology, Jining NO. 1 People's Hospital, Jining, 272000, People's Republic of China.
Wenxue SunInstitute of Clinical Pharmacy and Pharmacology, Jining NO. 1 People's Hospital, Jining Medical University, Jining, 272000, People's Republic of China.
Yuanyuan FengChildren's Rehabilitation Center, Jining Maternal and Child Health Family Planning Service Center, Jining, 272000, People's Republic of China.
Deshuai LiangDepartment of pharmacy, Jining NO. 1 People's Hospital, Jining, 272000, People's Republic of China.
Yun GuanDepartment of Hematology, Jining NO. 1 People's Hospital, Jining, 272000, People's Republic of China.
Jining First People's Hospital · CNAffiliated Hospital of Jining Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: We designed this study to investigate the potential correlations between gut microbiota compositions and hepatic metabolomic disorders in mice with methotrexate (MTX)-induced hepatoxicity. Methods: We used MTX to induce hepatoxicity in healthy Kunming mice, and we determined plasma ALT and AST levels and assessed the liver tissue histopathology. We applied an integrated gas chromatography-mass spectrometry (GC-MS) and 16S ribosomal RNA (rRNA) gene sequencing approach to evaluate the effects of MTX on the gut microbiota and hepatic metabolic profiles of mice. We uncovered correlations between the gut microbiota and hepatic metabolomic profiles by calculating the Spearman correlation coefficient. Results: MTX caused ALT and AST level elevations and hepatoxicity in our mouse model. MTX disrupted amino acid metabolic pathways (including biosyntheses of valine, leucine, and isoleucine; and arginine; and, metabolism of alanine, aspartate, and glutamate; histidine; beta-alanine; and glycine, serine, and threonine); biosyntheses of aminoacyl-tRNA; and pantothenate, and CoA; and, metabolic pathways of energy, glutathione, and porphyrin; and chlorophyll. In addition, MTX increased the abundances of Conclusion: We present evidence supporting the notion that MTX causes hepatoxicity by altering the gut microbiota and hepatic metabolite profiles, our findings provide new venues for the management of MTX-induced hepatoxicity.

Indexed as

Gastrointestinal MicrobiomeLiver DiseasesMicrobiotaAnimalsBacillotaMetabolomeMetabolomicsMethotrexateMiceMethotrexate16S ribosomal RNAgas chromatography-mass spectrometryhepatoxicitymethotrexate

Identifiers

PMID36388083
PMCPMC9653027
OpenAlexW4308374171

What OpenQuestion holds

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LicenceCC BY-NC
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.