Evidence map›Paper›PMID 32076940›Full record

ArticleInflammation2020

Salidroside Decreases Atherosclerosis Plaque Formation via Inhibiting Endothelial Cell Pyroptosis.

Sha-Sha Xing, Jin Yang, Wen-Jing Li, Jian Li, Lin Chen, Yu-Ting Yang, Xia Lei, Jun Li, Kai Wang, Xun Liu

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

37 citing papers in PubMed, 76 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Sha-Sha XingClinical Drug Trial Institution, Affiliated Hospital of Chengdu University, Chengdu, 610081, Sichuan, People's Republic of China.
Jin YangDepartment of Urology, Affiliated Hospital of Chengdu University, Chengdu, 610081, Sichuan, People's Republic of China. yangjincdfy@126.com.
Wen-Jing LiDepartment of Pharmacy, Zhongnan Hospital of Wuhan University, Wuhan, 430071, People's Republic of China.
Jian LiDepartment of Basic Medicine, Chengdu University School of Medicine, Chengdu, 610106, Sichuan, People's Republic of China.
Lin ChenDepartment of Urology, Affiliated Hospital of Chengdu University, Chengdu, 610081, Sichuan, People's Republic of China.
Yu-Ting YangClinical Drug Trial Institution, Affiliated Hospital of Chengdu University, Chengdu, 610081, Sichuan, People's Republic of China.
Xia LeiClinical Drug Trial Institution, Affiliated Hospital of Chengdu University, Chengdu, 610081, Sichuan, People's Republic of China.
Jun LiDepartment of General Surgery, Affiliated Hospital of Chengdu University, Chengdu University, Chengdu, 610081, Sichuan, People's Republic of China.
Kai WangDepartment of Urology, Affiliated Hospital of Chengdu University, Chengdu, 610081, Sichuan, People's Republic of China.
Xun LiuDepartment of Urology, Affiliated Hospital of Chengdu University, Chengdu, 610081, Sichuan, People's Republic of China.
Chengdu University · CNWuhan University · CN

Funding

Department of Science and Technology of Sichuan Province (CN) 2019YJ0654The Technology Bureau of Chengdu 2015-HM01-00434-SFThe Technology Bureau of Chengdu 2015-HM01-00580-SF
6 · The paper itself

Abstract

Pyroptosis, a new pro-inflammatory programmed cell death, is linked to atherosclerosis (AS). Our previous studies suggested that salidroside (SAL) can alleviate AS and exert anti-oxidative and anti-inflammatory properties. However, the effect of SAL on atherosclerosis-related pyroptosis has not been studied. Here, we investigated the effect of SAL on pyroptosis to explain the underlying mechanisms of SAL on atherosclerosis-related inflammation. We established an atherosclerosis mouse model via western diet (HFD) to explore the protective effect of SAL. According to our results, administration of SAL for 12 weeks markedly reduced the atherosclerotic plaque in aorta. Meanwhile, SAL also alleviated the pyroptosis, as evidenced by inhibiting caspase-1 activation, interleukin-1β (IL-1β) release, and TUNEL-positive staining, and decreasing the expression of Gasdermin D (GSDMD). Furthermore, SAL also decreased the activation of caspase-1 and inhibited the release of IL-1β induced by lipopolysaccharide (LPS) and adenosine triphosphate (ATP) in human umbilical vein endothelial cell (HUVECs). Our data indicate that SAL inhibit NLRP3-related pyroptosis, which might be the underlying mechanism of SAL anti-inflammatory in atherosclerosis.

Indexed as

RhodiolaAnimalsAtherosclerosisDose-Response Relationship, DrugGlucosidesHumansHuman Umbilical Vein Endothelial CellsMaleMiceMice, KnockoutPhenolsPlaque, AtheroscleroticPyroptosisGlucosidesPhenolsrhodiolosideendothelial cellsGSDMD, atherosclerosispyroptosissalidroside

Identifiers

PMID32076940
OpenAlexW3008669429

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.