Evidence map›Paper›PMID 31217872›Full record

ArticleAmerican journal of translational research2019

Hepatoprotective effect of capsaicin against concanavalin A-induced hepatic injury via inhibiting oxidative stress and inflammation.

Hui Zhang, Yang Bai, Min Gao, Junfeng Zhang, Guanjun Dong, Fenglian Yan, Qun Ma, Xingqin Fu, Qingqing Zhang, Chunxia Li and 8 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2019. 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
2.5field-weighted citation impact, top 10% 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, 31 citations in OpenAlex.

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  14. The Role of Serotonin in Concanavalin A-Induced Liver Injury in Mice.Oxidative medicine and cellular longevity · 2020
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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

18 authors at 3 institutions in 2 countries.

Hui ZhangInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Yang BaiDepartment of Urology, Jining First People's Hospital Jining 272011, Shandong Province, China.
Min GaoClinical Laboratory, Jining First People's Hospital Jining 272011, Shandong Province, China.
Junfeng ZhangInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Guanjun DongInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Fenglian YanInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Qun MaInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Xingqin FuInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Qingqing ZhangInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Chunxia LiInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Hui ShiInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Zhaochen NingInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Jun DaiInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Zhihua LiInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Jiankuo MingInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Qingjie XueInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Chuanping SiInstitute of Immunology and Molecular Medicine, Jining Medical University Jining 272067, Shandong Province, China.
Huabao XiongDepartment of Medicine, Precision Immunology Institute, Icahn School of Medicine at Mount Sinai New York, NY 10029, USA.
Jining Medical University · CNJining First People's Hospital · CNIcahn School of Medicine at Mount Sinai · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune-mediated liver injury plays a crucial role in the pathogenesis of liver diseases, which can result from viral infections, autoimmunity, alcohol intake, and drug use. Concanavalin A (Con A)-induced hepatitis is a well-characterized murine model with similar pathophysiology to that of human viral and autoimmune hepatitis. Capsaicin, a selective agonist of the transient potential vanilloid subfamily member 1 (TRPV1) receptor, exhibits anti-inflammatory effects on various causes of inflammation. In the present study, we investigated the effect of capsaicin on Con A-induced hepatitis. Capsaicin (1 mg/kg body weight) was administered by intraperitoneal injection, after which (30 minutes), the mice were challenged intravenously with Con A (20 μg/g body weight). We collected serum for plasma transaminase analysis. Pro-inflammatory cytokine levels and hepatocyte apoptosis were assayed by ELISA and TUNEL, respectively. Liver samples were collected for real-time PCR, hematoxylin and eosin staining, and measuring oxidative stress and myeloperoxidase levels. Activation of splenocytes and hepatic mononuclear cells was analyzed by flow cytometry. Compared with control, the capsaicin-treated group showed significantly decreased aminotransferase levels and markedly prolonged mouse survival. Capsaicin pretreatment also attenuated hepatocyte apoptosis and oxidative stress. Furthermore, tumor necrosis factor-α and interferon-γ levels in serum and liver were significantly suppressed, while the percentage of myeloid-derived suppressor cells increased after capsaicin pretreatment. Our findings indicate that capsaicin pretreatment protects mice from Con A-induced hepatic damage and is partially involved in inhibiting hepatocyte apoptosis, oxidative stress, and inflammatory mediators as well as regulating activation and recruitment of intrahepatic leukocytes.

Indexed as

capsaicinConcanavalin Ahepatitisinflammationoxidative stress

Identifiers

PMID31217872
PMCPMC6556673
OpenAlexW2990381665

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.