Evidence map›Paper›PMID 31531179›Full record

ArticleOxidative medicine and cellular longevity2019

Targeting IL-17A Improves the Dysmotility of the Small Intestine and Alleviates the Injury of the Interstitial Cells of Cajal during Sepsis.

Jing Li, Pengyu Kong, Chao Chen, Jing Tang, Xiaoming Jin, Jinglong Yan, Yufu Wang

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 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
1.2field-weighted citation impact, top 22% 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, 17 citations in OpenAlex.

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  9. Role of CD34 in inflammatory bowel disease.Frontiers in physiology · 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 2 countries.

Jing LiDepartment of Pathology and Electron Microscopy Center, Faculty of Basic Medical Science, Harbin Medical University, Harbin, China.
Pengyu KongDepartment of Orthopedics, Second Affiliated Hospital, Harbin Medical University, Harbin, China.
Chao ChenDepartment of Medical Microbiology and Immunology, University of Alberta, Edmonton, Alberta, Canada.
Jing TangDepartment of Pathology and Electron Microscopy Center, Faculty of Basic Medical Science, Harbin Medical University, Harbin, China.
Xiaoming JinDepartment of Pathology and Electron Microscopy Center, Faculty of Basic Medical Science, Harbin Medical University, Harbin, China.ORCID https://orcid.org/0000-0003-1531-3803
Jinglong YanDepartment of Orthopedics, Second Affiliated Hospital, Harbin Medical University, Harbin, China.ORCID https://orcid.org/0000-0003-0288-6290
Yufu WangDepartment of Orthopedics, Second Affiliated Hospital, Harbin Medical University, Harbin, China.ORCID https://orcid.org/0000-0002-5513-8205
Harbin Medical University · CNUniversity of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal dysmotility is a frequent complication during sepsis and plays an important role in the development of secondary infections and multiple organ failure. However, the central mechanisms underlying this process have not been well elucidated. Currently, effective therapies are still lacking for the treatment of sepsis-induced intestinal dysmotility. In this study, we found that the activation of IL-17 signaling within the muscularis propria might be associated with dysmotility of the small intestine during polymicrobial sepsis. Furthermore, we demonstrated that targeting IL-17A partially rescued the motility of the small intestine and alleviated interstitial cells of Cajal (ICC) injury during sepsis. The blockade of IL-17A suppressed the dominant sepsis-induced infiltration of M1-polarized macrophages into the muscularis. Additionally, impaired ICC survival may be associated with the oxidative stress injury induced by dominant infiltration of M1-polarized macrophages. Our findings reveal the important role of the IL-17 signaling pathway in the small intestine during sepsis and provide clues for developing a novel therapeutic strategy for treating gastrointestinal dysmotility during sepsis.

Indexed as

AnimalsFemaleGastrointestinal MotilityInterleukin-17Interstitial Cells of CajalIntestine, SmallMaleMiceRAW 264.7 CellsSepsisSignal TransductionIl17a protein, mouseInterleukin-17

Identifiers

PMID31531179
PMCPMC6721283
OpenAlexW2967777612

What OpenQuestion holds

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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.