Evidence map›Paper›PMID 36737780›Full record

ArticleJournal of inflammation (London, England)2023

Tofacitinib reduces acute lung injury and improves survival in a rat model of sepsis by inhibiting the JAK-STAT/NF-κB pathway.

Xinxin Zhang, Xingsheng Wang, Li Sun, Guangsheng Gao, Yun Li

Open access · goldAbstract read
In one paragraph

Article in Journal of inflammation (London, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Review
  8. Acute Lung Injury and the NLRP3 Inflammasome.Journal of inflammation research · 2024
    Review
  9. Review
  10. Review
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

5 authors at 3 institutions in 1 country.

Xinxin ZhangDepartment of Emergency Medicine, Fuyang People's Hospital of Anhui Medical University, Fuyang, Anhui, China.
Xingsheng WangIntensive Care Unit, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Li SunDepartment of Health Care, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Guangsheng GaoIntensive Care Unit, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China. zxyysean2022@163.com.
Yun LiIntensive Care Unit, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China. Yunlee2022@163.com.
Jinan Central Hospital · CNAnhui Medical University · CNShandong First Medical University · CN

Funding

Academic promotion programme of Shandong First Medical University 2019QL024
6 · The paper itself

Abstract

Acute lung injury is a major cause of death in sepsis. Tofacitinib (TOFA), a JAK inhibitor, has anti-inflammatory activity in autoimmune diseases, but its role in acute lung injury in sepsis remains unclear. The purpose of this study is to establish a septic rat model by cecal ligation and perforation, and to evaluate the effect of tofacitinib on the survival rate of septic rat model and its role in acute lung injury in septic rats and the possible mechanism of action. In this study, TOFA (1 mg/kg, 3 mg/kg, 10 mg/kg) was used to observe the survival rate of septic rats. It was found that TOFA (10 mg/kg) significantly improved the survival rate of septic rats. We selected TOFA (10 mg/kg) and focused on the protective effect of TOFA on acute lung injury. The results confirmed that TOFA significantly inhibited the expression of TNF-α, IL-1β, IL-6 and IFN-γ inflammatory factors, reduced the W/D weight ratio of septic lung tissue, and significantly improved lung histopathological damage. These results may be related to the inhibitory effect of TOFA on JAK-STAT/NF-κ B signaling pathway. In conclusion, for the first time, we found that TOFA has a protective effect against sepsis-induced acute lung injury, and it may be a promising drug for the treatment of acute lung injury in sepsis.

Indexed as

Cecum ligation perforationJAK-STATNF-κ BSepsisTofacitinib

Identifiers

PMID36737780
PMCPMC9896809
OpenAlexW4319080466

What Socratic 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 Socratic graph.