Evidence map›Paper›PMID 34860135›Full record

ArticleBioengineered2021

Rotigotine protects against oxidized low-density lipoprotein(ox-LDL)-induced damages in human umbilical vein endothelial cells(HUVECs).

Hui Kang, Hui Yu, Jingxiu Fan, Ge Cao

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Review of OxLDL Driven Inflammatory Cell Activation.Current atherosclerosis reports · 2025
    Pooled it
  2. Article
  3. PeerJ · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Anti-Inflammatory Effects of Peripheral Dopamine.International journal of molecular sciences · 2023
    Review
  9. Article
  10. The Potential Role of Connexins in the Pathogenesis of Atherosclerosis.International journal of molecular sciences · 2023
    Review
  11. Therapeutic effects ofBioengineered · 2022
    Article
  12. 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

4 authors at 1 institution in 1 country.

Hui KangDepartment of Cardiovascular Surgery, West China Hospital of Sichuan University, Chengdu, China.
Hui YuDepartment of Cardiovascular Surgery, West China Hospital of Sichuan University, Chengdu, China.
Jingxiu FanDepartment of Cardiovascular Surgery, West China Hospital of Sichuan University, Chengdu, China.
Ge CaoDepartment of Cardiovascular Surgery, West China Hospital of Sichuan University, Chengdu, China.ORCID 0000-0003-3766-8170
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rotigotine is a non-ergoline dopamine agonist that has been licensed for the treatment of Parkinson's disease. Cardiovascular diseases are the world's leading cause of death. Ox-LDL- induced endothelial damages are involved in the initiation and progression of cardiovascular diseases. In this study, we assessed the beneficial properties of Rotigotine on ox-LDL-induced insults to HUVECs to highlight its potential use in the treatment of cardiovascular diseases. Our findings show that Rotigotine suppresses the expressions of low-density lipoprotein receptor (LDL-R), proprotein convertase subtilisin/kexin type 9 (PCSK-9), and sterol regulatory element-binding protein (SREBP-2). It also inhibits ox-LDL-induced cholesterol accumulation in endothelial cells (ECs), improves U937 monocytes adhesion, and decreases the representation of NADPH oxidase (NOX-4) and generation of reactive oxygen species (ROS) in endothelial cells (ECs). Furthermore, Rotigotine inhibited the expressions of both vascular cellular adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) in HUVECs and had anti-inflammatory efficacy in ox-LDL-induced cells by inhibiting the expressions of pro-inflammatory cytokines. Notably, Rotigotine inhibits the activation of nuclear factor-kappaB (NF-κB) by preventing nuclear translocation of NF-κB p65 and reducing the luciferase activity of NF-κB reporter. We, therefore, conclude that these effects of Rotigotine on HUVECs suggest that it may play a therapeutic role in cardiovascular diseases.

Indexed as

Cell Adhesion MoleculesCell DeathCholesterolCytokinesHumansHuman Umbilical Vein Endothelial CellsInflammation MediatorsLipoproteins, LDLMonocytesNF-kappa BOxidative StressProprotein Convertase 9Protective AgentsReceptors, LDLSterol Regulatory Element Binding Protein 2TetrahydronaphthalenesCell Adhesion MoleculesCholesterolCytokinesInflammation MediatorsLipoproteins, LDLNF-kappa Boxidized low density lipoproteinPCSK9 protein, humanProprotein Convertase 9Protective AgentsReceptors, LDLrotigotineSREBF2 protein, humanSterol Regulatory Element Binding Protein 2TetrahydronaphthalenesThiophenesCardiovascular diseasesHUVECsNF-κBox-LDLRotigotine

Identifiers

PMID34860135
PMCPMC8810014
OpenAlexW3216243528

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.