Evidence map›Paper›PMID 35759238›Full record

ArticleImmunity, inflammation and disease2022

Inducible nitric oxide synthase regulates macrophage polarization via the MAPK signals in concanavalin A-induced hepatitis.

Xiaoying Yao, Guiyuan Jin, Dong Liu, Xiaobei Zhang, Yonghong Yang, Yu Chen, Zhongping Duan, Yanzhen Bi, Fenglian Yan, Yanli Yang and 7 more

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 17 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

17 authors at 5 institutions in 2 countries.

Xiaoying YaoMedical Research Center, Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Guiyuan JinMedical Research Center, Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Dong LiuDepartment of Clinical Laboratory, Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Xiaobei ZhangMedical Research Center, Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Yonghong YangMedical Research Center, Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Yu ChenFourth Liver Disease Center, Beijing YouAn Hospital, Capital Medical University, Beijing, China.
Zhongping DuanFourth Liver Disease Center, Beijing YouAn Hospital, Capital Medical University, Beijing, China.
Yanzhen BiDepartment of Infectious Disease, Qingdao Municipal Hospital, Qingdao, Shandong, China.
Fenglian YanInstitute of Immunology and Molecular Medicine, Jining Medical University, Jining, Shandong, China.
Yanli YangInstitute of Immunology and Molecular Medicine, Jining Medical University, Jining, Shandong, China.
Hui ZhangInstitute of Immunology and Molecular Medicine, Jining Medical University, Jining, Shandong, China.
Guanjun DongInstitute of Immunology and Molecular Medicine, Jining Medical University, Jining, Shandong, China.
Shanshan LiFourth Liver Disease Center, Beijing YouAn Hospital, Capital Medical University, Beijing, China.
Shumin ChengDepartment of Gastroenterology, People's Hospital of Jia Xiang, Jining, Shandong, China.
Huixin TangMedical Research Center, Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Feng HongMedical Research Center, Affiliated Hospital of Jining Medical University, Jining, Shandong, China.
Chuanping SiInstitute of Immune Precision Diagnosis and Therapy & Translational Medicine, Affiliated Hospital of Jining Medical University, Jining, Shandong, China.ORCID 0000-0001-7539-5092
Affiliated Hospital of Jining Medical University · CNCapital Medical University · CNJining Medical University · CNZero to Three · USQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAcute liver inflammatory reactions contribute to many health problems; thus, it is critical to understand the underlying pathogenic mechanisms of acute hepatitis. In this study, an experimental in vivo model of concanavalin A (ConA)-induced hepatitis was used. MATERIALS AND

methodsC57BL/6 (wild-type, WT) or inducible nitric oxide synthase-deficient (iNOS

resultsiNOS

conclusioniNOS may contribute to ConA-induced inflammation by promoting the activation of proinflammatory macrophages.

Indexed as

HepatitisAnimalsConcanavalin AInflammationMacrophagesMiceMice, Inbred C57BLNitric Oxide Synthase Type IIConcanavalin ANitric Oxide Synthase Type IIhepatitisiNOSmacrophagemitogen-activated protein kinase

Identifiers

PMID35759238
PMCPMC9168548
OpenAlexW4281724030

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.