Evidence map›Paper›PMID 29393437›Full record

ArticleMolecular medicine reports2018

Polysaccharide from Fuzi protects against Ox‑LDL‑induced calcification of human vascular smooth muscle cells by increasing autophagic activity.

Lizhen Liao, Xiaodong Zhuang, Weidong Li, Qibiao Su, Jie Zhao, Ying Liu

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. New insight into dyslipidemia-induced cellular senescence in atherosclerosis.Biological reviews of the Cambridge Philosophical Society · 2022
    Review
  3. Processed lateral root ofFrontiers in pharmacology · 2022
    Review
  4. Review
  5. Article
  6. Article
  7. Review
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

6 authors at 2 institutions in 1 country.

Lizhen Liao *Guangdong Pharmaceutical University, Guangzhou Higher Education Mega Center, Guangzhou, Guangdong 510006, P.R. China.
Xiaodong Zhuang *Department of Cardiology, The First Affiliated Hospital of Sun Yat‑sen University, Guangzhou, Guangdong 510080, P.R. China.
Weidong LiGuangdong Pharmaceutical University, Guangzhou Higher Education Mega Center, Guangzhou, Guangdong 510006, P.R. China.
Qibiao SuGuangdong Pharmaceutical University, Guangzhou Higher Education Mega Center, Guangzhou, Guangdong 510006, P.R. China.
Jie ZhaoGuangdong Pharmaceutical University, Guangzhou Higher Education Mega Center, Guangzhou, Guangdong 510006, P.R. China.
Ying LiuGuangdong Pharmaceutical University, Guangzhou Higher Education Mega Center, Guangzhou, Guangdong 510006, P.R. China.
Guangdong Pharmaceutical University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polysaccharide from Fuzi (FPS) is a water‑soluble polysaccharide isolated from the traditional Chinese herbal medicine Fuzi. It has been demonstrated to protect hepatocytes against ischemia‑reperfusion injury through its potent antioxidant effects, and to attenuate starvation‑induced cytotoxicity in H9c2 cells by increasing autophagic activity. In the present study, Alizarin Red S staining was used to detect mineral deposition and reverse transcription‑quantitative polymerase chain reaction was used to detect the core binding factor α1 and smooth muscle 22α mRNA expression. To analyze autophagic activity, western blotting was used to detect microtubule‑associated protein 1A/1B light chain 3 and nucleoporin P62 expression. In addition, green fluorescent protein‑LC3 dots‑per‑cell was observed by fluorescence microscopy. It was demonstrated that oxidized low‑density lipoprotein (Ox‑LDL) could increase the calcification of human vascular smooth muscle cells (VSMCs) in a concentration‑dependent manner, and that FPS treatment had a significant protective effect against Ox‑LDL‑induced calcification of human VSMCs. Furthermore, FPS treatment alleviated the Ox‑LDL‑induced downregulation of autophagic activity, and the protective effect of FPS on Ox‑LDL‑induced calcification was attenuated by the autophagy inhibitor 3‑methyladenine. In conclusion, the present study demonstrated for the first time to the best of the authors' knowledge that FPS can protect against Ox‑LDL‑induced vascular calcification in human VSMCs, and that this likely occurs via the activation of autophagy. This supports the hypothesis that autophagy may be an endogenous protective mechanism counteracting vascular calcification, and that FPS may be used as a potential therapeutic for vascular calcification.

Indexed as

AdenineAutophagyDiterpenesDrugs, Chinese HerbalHumansLipoproteins, LDLMuscle, Smooth, VascularMyocytes, Smooth MusclePlant ExtractsPolysaccharidesVascular Calcification3-methyladenineAdenineDiterpenesDrugs, Chinese Herbalfuzi drug herbalLipoproteins, LDLoxidized low density lipoproteinPlant ExtractsPolysaccharidesautophagycalcificationhuman vascular smooth muscle cellpolysaccharide from Fuzi

Identifiers

PMID29393437
PMCPMC5865975
OpenAlexW2788592833

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.