Evidence map›Paper›PMID 39654025›Full record

ArticleJournal of cellular and molecular medicine2024

Schisandrin B Inhibits LPS-Induced Endometritis Through Attenuating Ferroptosis via AMPK/PGC1α/Nrf2 Signalling Pathway.

Jing Yu, Xuewei Li, Min Zhou, Min Lu, Zheng Ruan, Wenshuang Zou, Shaohui Yu

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Astragaloside IV AlleviatesAntioxidants (Basel, Switzerland) · 2026
    Article
  4. Article
  5. 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.

Jing YuDepartment of Endocrinology, Affiliated Hospital of Changchun University of Traditional Chinese Medicine, Changchun, Jilin, China.
Xuewei LiDepartment of Gynaecology, Affiliated Hospital of Changchun University of Traditional Chinese Medicine, Changchun, Jilin, China.
Min ZhouDepartment of Gynaecology, Affiliated Hospital of Changchun University of Traditional Chinese Medicine, Changchun, Jilin, China.
Min LuDepartment of Gynaecology, Affiliated Hospital of Changchun University of Traditional Chinese Medicine, Changchun, Jilin, China.
Zheng RuanDepartment of Traditional Chinese Medicine, 964th Hospital, Changchun, China.
Wenshuang ZouDepartment of Gastroenterology, The Affiliated Hospital to Changchun University of Chinese Medicine, Changchun, Jilin, People's Republic of China.
Shaohui YuDepartment of Gynaecology, Affiliated Hospital of Changchun University of Traditional Chinese Medicine, Changchun, Jilin, China.ORCID 0009-0000-2007-2819

Funding

Science and Technology Project of the Jilin Provincial Department of Education JJKH20230960KJ
6 · The paper itself

Abstract

Endometritis is one of the common reproductive diseases in human and animal. In recent years, a number of studies have found that Schisandra B (Sch B), as a natural Chinese medicine extract, has antioxidant, anti-inflammatory and other biological activities. Based on the above, in this study, mice were used to conduct an in vivo experiment to investigate the effect and mechanism of Sch B on lipopolysaccharide (LPS)-induced endometritis. Haematoxylin and eosin (H&E) staining was used to detect the pathological changes of uterine tissue and western blot was used to detect the expression levels of signalling pathways and key genes for ferroptosis. The results showed that Sch B significantly inhibited the pathological injury of uterine tissue, myeloperoxidase (MPO) activity, the activation of NF-κB pathway and the production of TNF-α and IL-1β. Furthermore, Sch B effectively inhibited ferroptosis by inhibiting malondialdehyde (MDA) and iron production and promoting the expression of ferroptosis suppressor genes GPX4 and ferritin. In conclusion, Sch B inhibited LPS-induced endometritis through alleviating inflammatory response and ferroptosis via AMPK/PGC1α/Nrf2 signalling pathway.

Indexed as

AMP-Activated Protein KinasesCyclooctanesEndometritisFerroptosisLignansLipopolysaccharidesNF-E2-Related Factor 2Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPolycyclic CompoundsSignal TransductionAnimalsFemaleInterleukin-1betaMiceNF-kappa BAMP-Activated Protein KinasesCyclooctanesInterleukin-1betaLignansLipopolysaccharidesNfe2l2 protein, mouseNF-E2-Related Factor 2NF-kappa BPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPolycyclic CompoundsPpargc1a protein, mouseschizandrin BendometritisferroptosisinflammationLPSSchisandra B

Identifiers

PMID39654025
PMCPMC11628352

What OpenQuestion holds

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Registered trials

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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.