Evidence map›Paper›PMID 27878684›Full record

ArticleInflammation2017

Bakuchiol Protects Against Acute Lung Injury in Septic Mice.

Xinxin Zhang, Ning Chang, Yong Zhang, Mingxiang Ye, Zhiping Han, Jie Li, Jian Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 37 citations in OpenAlex.

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  12. Downregulation of miR-155 attenuates sepsis-induced acute lung injury by targeting SIRT1.International journal of clinical and experimental pathology · 2018
    Article
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 1 country.

Xinxin ZhangDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, #127 Changle West Road, Xi'an, 710032, People's Republic of China.
Ning ChangDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, #127 Changle West Road, Xi'an, 710032, People's Republic of China.
Yong ZhangDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, #127 Changle West Road, Xi'an, 710032, People's Republic of China.
Mingxiang YeDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, #127 Changle West Road, Xi'an, 710032, People's Republic of China.
Zhiping HanDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, #127 Changle West Road, Xi'an, 710032, People's Republic of China.
Jie LiDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, #127 Changle West Road, Xi'an, 710032, People's Republic of China.
Jian ZhangDepartment of Pulmonary Medicine, Xijing Hospital, Fourth Military Medical University, #127 Changle West Road, Xi'an, 710032, People's Republic of China. fmmuzj1970@163.com.
Xijing Hospital · CNAir Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is a systemic inflammatory reaction that may lead to multiple organ damage and acute lung injury (ALI). Bakuchiol (Bak) has been reported to confer protection against inflammation and oxidative stress. However, its effect on sepsis-induced acute lung injury remains unclear. In the present study, male C57BL/6 mice were subjected to cecal ligation and puncture (CLP), and Bak (15, 30, 60 mg/kg) was administered intragastrically after 0 and 3 h of surgery. Lung water content was detected. Pathologic changes in lung tissues were evaluated via hematoxylin and eosin (H&E) staining. The levels of myeloperoxidase (MPO), IL-1β, IL-6, and TNF-α were evaluated using ELISA. In addition, expression levels of phosphorylated (p)-IκB, ICAM-1, HMGB1, nitrotyrosine (3-NT), claudin-1, and VE-cadherin were detected using Western blot. Further, IL-1β expression was evaluated using immunofluorescence. SOD activity, contents of MDA, and 8-OHdG were detected to determine the level of oxidative stress. Our results suggested that Bak (60 mg/kg) treatment significantly attenuated pathologic changes and edema in lung tissues and attenuated inflammation and oxidative stress in the lung following sepsis. Additionally, Bak treatment alleviated sepsis-induced lung endothelial barrier disruption. In conclusion, Bak treatment attenuates ALI following sepsis by suppressing inflammation, oxidative stress, and endothelial barrier disruption. Our study indicates that Bak is a potential candidate to treat sepsis-induced ALI.

Indexed as

Acute Lung InjuryAnimalsEdemaEndotheliumInflammationLungMaleMiceMice, Inbred C57BLOxidative StressPhenolsProtective AgentsSepsisbakuchiolPhenolsProtective Agentsacute lung injurybakuchiolcecal ligation and puncturesepsis

Identifiers

PMID27878684
OpenAlexW2551760327

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.