Evidence map›Paper›PMID 39146322›Full record

ArticlePloS one2024

Atorvastatin inhibits Lipopolysaccharide (LPS)-induced vascular inflammation to protect endothelium by inducing Heme Oxygenase-1 (HO-1) expression.

Jian Luo, Qian Zhu, Keming Huang, Xue Wen, Yongquan Peng, Gong Chen, Gang Wei

Erratum issuedAbstract read
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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Jian LuoDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Lu Zhou, China.
Qian ZhuDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Lu Zhou, China.
Keming HuangDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Lu Zhou, China.
Xue WenDepartment of Laboratory Medicine, The Affiliated Hospital of Southwest Medical University, Lu Zhou, China.
Yongquan PengDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Lu Zhou, China.
Gong ChenDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Lu Zhou, China.ORCID 0009-0000-6477-381X
Gang WeiDepartment of Cardiology, The Affiliated Hospital of Southwest Medical University, Lu Zhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aimed to explore the differential effects of varying doses of atorvastatin on antagonizing lipopolysaccharide (LPS)-induced endothelial inflammation based on heme oxygenase 1 (HO-1) expression.

methodVascular endothelial inflammatory injury was induced in 40 Sprague-Dawley rats by intraperitoneal injection of LPS. These rats were randomly divided into control, low-dose atorvastatin, high-dose atorvastatin, and HO-1 blocking groups. Seven days after treatment, all rats were sacrificed, and heart-derived peripheral blood was collected to measure the serum concentrations of bilirubin, alanine aminotransferase (ALT), total cholesterol, malondialdehyde, endothelial cell protein C receptor, endothelin-1, von Willebrand factor, and soluble thrombomodulin. Meanwhile, the number of circulating endothelial cells was determined using flow cytometry. Vascular tissues from descending aorta of rats from each group were extracted to detect the expression level of HO-1.

resultsAfter different doses of atorvastatin intervention, the above inflammatory indices were decreased, and HO-1 expression and ALT concentration were increased in the atorvastatin-treated group of rats compared with the control group. These changes were more pronounced in the high-dose statin group (P < 0.05). Conversely, no significant decrease in the above inflammatory indices and no significant increase in HO-1 expression were observed in rats in the blocking group (P > 0.05).

conclusionFor LPS-induced vascular inflammation, high-dose atorvastatin exerts potent anti-inflammatory and vascular endothelial protection effects by inducing HO-1 expression.

Indexed as

AtorvastatinEndothelium, VascularLipopolysaccharidesRats, Sprague-DawleyAlanine TransaminaseAnimalsHeme Oxygenase-1Heme Oxygenase (Decyclizing)InflammationMaleRatsAlanine TransaminaseAtorvastatinHeme Oxygenase-1Heme Oxygenase (Decyclizing)Hmox1 protein, ratLipopolysaccharides

Identifiers

PMID39146322
PMCPMC11326635

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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.