Evidence map›Paper›PMID 33859560›Full record

ArticleFrontiers in pharmacology2021

Mahuang Decoction Antagonizes Acute Liver Failure via Modulating Tricarboxylic Acid Cycle and Amino Acids Metabolism.

Wenting Liao, Qiwen Jin, Junning Liu, Yiling Ruan, Xinran Li, Yueyue Shen, Zhicheng Zhang, Yong Wang, Shengming Wu, Junying Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 24 citations in OpenAlex.

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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

12 authors at 4 institutions in 2 countries.

Wenting LiaoDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Qiwen JinDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Junning LiuInstitute of Forensic Science, Nanjing Municipal Public Security Bureau, Nanjing, China.
Yiling RuanDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Xinran LiDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Yueyue ShenDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
Zhicheng ZhangInstitute of Forensic Science, Nanjing Municipal Public Security Bureau, Nanjing, China.
Yong WangInstitute of Forensic Science, Nanjing Municipal Public Security Bureau, Nanjing, China.
Shengming WuNanjing Liuhe District Hospital of Traditional Chinese Medicine, Nanjing, China.
Junying ZhangDepartment of TCMs Pharmaceuticals, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, China.
Lifeng KangFaculty of Medicine and Health, School of Pharmacy, University of Sydney, Sydney, NSW, Australia.
Chunyong WuDepartment of Pharmaceutical Analysis, China Pharmaceutical University, Nanjing, China.
China Pharmaceutical University · CNInstitute of Forensic Science · CNNanjing Traditional Chinese Medicine Hospital · CNUniversity of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute liver failure (ALF) is a serious clinical disorder with high fatality rates. Mahuang decoction (MHD), a well-known traditional Chinese medicine, has multiple pharmacological effects, such as anti-inflammation, anti-allergy, anti-asthma, and anti-hyperglycemia. In this study, we investigated the protective effect of MHD against ALF. In the lipopolysaccharide and D-galactosamine (LPS/D-GalN)-induced ALF mouse model, the elevated activities of the serum alanine and aspartate transaminases as well as the liver pathological damage were markedly alleviated by MHD. Subsequently, a metabolomics study based on the ultrahigh performance liquid chromatograph coupled with Q Exactive Orbitrap mass spectrometry was carried to clarify the therapeutic mechanisms of MHD against ALF. A total of 36 metabolites contributing to LPS/D-GalN-induced ALF were identified in the serum samples, among which the abnormalities of 27 metabolites were ameliorated by MHD. The analysis of metabolic pathways revealed that the therapeutic effects of MHD are likely due to the modulation of the metabolic disorders of tricarboxylic acid (TCA) cycle, retinol metabolism, tryptophan metabolism, arginine and proline metabolism, nicotinate and nicotinamide metabolism, phenylalanine metabolism, phenylalanine, tyrosine and tryptophan synthesis, as well as cysteine and methionine metabolism. This study demonstrated for the first time that MHD exerted an obvious protective effect against ALF mainly through the regulation of TCA cycle and amino acid metabolism, highlighting the importance of metabolomics to investigate the drug-targeted metabolic pathways.

Indexed as

acute liver failureamino acids metabolismmahuang decoctionmetabolomicstricarboxylic acid cycleUPLC-Q-exactive-MS

Identifiers

PMID33859560
PMCPMC8043081
OpenAlexW3142475811

What Socratic holds

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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 Socratic graph.