Evidence map›Paper›PMID 29243040›Full record

ArticleArchives of pharmacal research2018

Protective effect of acacetin on sepsis-induced acute lung injury via its anti-inflammatory and antioxidative activity.

Li-Chao Sun, Hong-Bo Zhang, Cheng-Dong Gu, Shi-Dong Guo, Gang Li, Rui Lian, Yao Yao, Guo-Qiang Zhang

Abstract read
In one paragraph

Article in Archives of pharmacal research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

38 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
  2. Comparative Analysis of Anti-Inflammatory Flavones inMolecules (Basel, Switzerland) · 2025
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  14. Can natural products modulate cytokine storm in SARS-CoV2 patients?Biotechnology reports (Amsterdam, Netherlands) · 2022
    Review
  15. Article
  16. Article
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  18. Article
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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

8 authors at 1 institution in 1 country.

Li-Chao SunEmergency Department of China-Japan Friendship Hospital, 2 Yinghua Dongjie, Chaoyang District, Hepingli, Beijing, 100029, China.
Hong-Bo ZhangEmergency Department of China-Japan Friendship Hospital, 2 Yinghua Dongjie, Chaoyang District, Hepingli, Beijing, 100029, China.
Cheng-Dong GuEmergency Department of China-Japan Friendship Hospital, 2 Yinghua Dongjie, Chaoyang District, Hepingli, Beijing, 100029, China.
Shi-Dong GuoEmergency Department of China-Japan Friendship Hospital, 2 Yinghua Dongjie, Chaoyang District, Hepingli, Beijing, 100029, China.
Gang LiEmergency Department of China-Japan Friendship Hospital, 2 Yinghua Dongjie, Chaoyang District, Hepingli, Beijing, 100029, China.
Rui LianEmergency Department of China-Japan Friendship Hospital, 2 Yinghua Dongjie, Chaoyang District, Hepingli, Beijing, 100029, China.
Yao YaoEmergency Department of China-Japan Friendship Hospital, 2 Yinghua Dongjie, Chaoyang District, Hepingli, Beijing, 100029, China.
Guo-Qiang ZhangEmergency Department of China-Japan Friendship Hospital, 2 Yinghua Dongjie, Chaoyang District, Hepingli, Beijing, 100029, China. guo_qinag_zhang@126.com.
China-Japan Friendship Hospital · CN

Funding

Chin-Japan Friendship Hospital project 2015-1-QN-22National Natural Science Foundation of China 81601725
6 · The paper itself

Abstract

Sepsis is a clinical syndrome with no effective protective or therapeutic treatments. Acacetin, a natural flavonoid compound, has anti-oxidative and anti-inflammatory effects which can potentially work to reduce sepsis. We investigated the potential protective effect of acacetin on sepsis-induced acute lung injury (ALI) ALI and dissect out the underlying mechanisms. Mice were divided into five groups: a sham group, a sepsis-induced ALI group, and three sepsis groups pre-treated with 20, 40, and 80 mg/kg body weight of acacetin. We found that acacetin significantly attenuated sepsis-induced ALI, in histological examinations and lung edema. Additionally, acacetin treatment decreased protein and inflammatory cytokine concentration and the number of infiltrated inflammatory cells in BALF compared with that in the non-treated sepsis mice. Pulmonary myeloperoxidase (MPO) activity was lower in the acacetin-pre-treated sepsis groups than in the sepsis group. The mechanism underlying the protective effect of acacetin on sepsis is related to the regulation of certain antioxidation genes, including inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), superoxide dismutases (SODs), and heme oxygenase 1 (HO-1).Taken together, our results indicate that acacetin pre-treatment inhibits sepsis-induced ALI through its anti-inflammatory and antioxidative activity, suggesting that acacetin may be a potential protective agent for sepsis-induced ALI.

Indexed as

Acute Lung InjuryAnimalsAnti-Inflammatory Agents, Non-SteroidalAntioxidantsCells, CulturedCytokinesEdemaFemaleFlavonesMiceMice, Inbred C57BLPeroxidaseProtective AgentsRAW 264.7 CellsSepsisacacetinAnti-Inflammatory Agents, Non-SteroidalAntioxidantsCytokinesFlavonesPeroxidaseProtective AgentsAcacetinCOX-2iNOSSepsisSODs

Identifiers

PMID29243040
PMCPMC7101724
OpenAlexW2772245075

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.