Evidence map›Paper›PMID 32630640›Full record

ReviewAntioxidants (Basel, Switzerland)2020

Perivascular Adipose Tissue as a Target for Antioxidant Therapy for Cardiovascular Complications.

Andy W C Man, Yawen Zhou, Ning Xia, Huige Li

Open access · goldAbstract readReview
In one paragraph

Review in Antioxidants (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Adipokine Nesfatin-1 Mediates Endothelial Dysfunction by SuppressingJournal of the American Heart Association · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Brown AlgaeMarine drugs · 2024
    Article
  13. Review
  14. Article
  15. Effects of gold nanoparticles phytoreduced withMedicine and pharmacy reports · 2024
    Article
  16. Article
  17. Review
  18. Article
  19. Perivascular Adipose Tissue Oxidative Stress in Obesity.Antioxidants (Basel, Switzerland) · 2023
    Review
  20. 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

4 authors at 1 institution in 1 country.

Andy W C ManDepartment of Pharmacology, Johannes Gutenberg University Medical Center, 55131 Mainz, Germany.ORCID 0000-0002-4113-6479
Yawen ZhouDepartment of Pharmacology, Johannes Gutenberg University Medical Center, 55131 Mainz, Germany.
Ning XiaDepartment of Pharmacology, Johannes Gutenberg University Medical Center, 55131 Mainz, Germany.
Huige LiDepartment of Pharmacology, Johannes Gutenberg University Medical Center, 55131 Mainz, Germany.ORCID 0000-0003-3458-7391
Johannes Gutenberg University Mainz · DE

Funding

Boehringer Ingelheim Stiftung CardioConsortium "Novel and neglected cardiovascular risk factors: molecular mechanisms and therapeutic implications"Deutsche Forschungsgemeinschaft LI-1042/1-1, LI-1042/3-1, LI-1042/5-1, and XI 139/2-1
6 · The paper itself

Abstract

Perivascular adipose tissue (PVAT) is the connective tissue surrounding most of the systemic blood vessels. PVAT is now recognized as an important endocrine tissue that maintains vascular homeostasis. Healthy PVAT has anticontractile, anti-inflammatory, and antioxidative roles. Vascular oxidative stress is an important pathophysiological event in cardiometabolic complications of obesity, type 2 diabetes, and hypertension. Accumulating data from both humans and experimental animal models suggests that PVAT dysfunction is potentially linked to cardiovascular diseases, and associated with augmented vascular inflammation, oxidative stress, and arterial remodeling. Reactive oxygen species produced from PVAT can be originated from mitochondria, nicotinamide adenine dinucleotide phosphate (NADPH) oxidases, and uncoupled endothelial nitric oxide synthase. PVAT can also sense vascular paracrine signals and response by secreting vasoactive adipokines. Therefore, PVAT may constitute a novel therapeutic target for the prevention and treatment of cardiovascular diseases. In this review, we summarize recent findings on PVAT functions, ROS production, and oxidative stress in different pathophysiological settings and discuss the potential antioxidant therapies for cardiovascular diseases by targeting PVAT.

Indexed as

cardiovascular diseasesendothelial nitric oxide synthasemetabolic diseasesoxidative stressperivascular adipose tissuesirtuin 1

Identifiers

PMID32630640
PMCPMC7402161
OpenAlexW3038177318

What Socratic 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 Socratic graph.