Evidence map›Paper›PMID 25385496›Full record

ArticleLipids2014

Vitamin E conditionally inhibits atherosclerosis in ApoE knockout mice by anti-oxidation and regulation of vasculature gene expressions.

Futian Tang, Meili Lu, Suping Zhang, Meng Mei, Tieqiao Wang, Peiqing Liu, Hongxin Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Lipids, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Vitamin E: Where Are We Now in Vascular Diseases?Life (Basel, Switzerland) · 2022
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Insights on Localized and Systemic Delivery of Redox-Based Therapeutics.Oxidative medicine and cellular longevity · 2018
    Review
  12. Oxidative Stress: Harms and Benefits for Human Health.Oxidative medicine and cellular longevity · 2017
    Review
  13. Review
  14. Article
  15. 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

7 authors at 2 institutions in 1 country.

Futian TangKey Laboratory of Cardio- and Cerebro-vascular Drug Research of Liaoning Province of Drug Research Institute, Liaoning Medical University, Jinzhou, 121001, China.
Meili Lu
Suping Zhang
Meng Mei
Tieqiao Wang
Peiqing Liu
Hongxin Wang
Jinzhou Medical University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipid deposition in artery walls is implied in the pathogenesis of atherosclerosis and imbalance between uptake and efflux of cholesterol favors the deposition. We investigated the effect of vitamin E with the same dose and duration on the different stages of atherosclerosis in Apolipoprotein E knockout (ApoE KO) mice and explored the potential mechanisms. The results showed that the ApoE KO mouse spontaneously develops atherosclerosis in an age-dependent manner from 14 to 46 weeks on the regular chow. Vitamin E (100 mg/kg) supplementation to ApoE KO mice at 6, 14, and 22 weeks for 8 weeks significantly reduced the atherosclerotic lesion area by 41, 29 and 19% respectively compared to the age-matched control mice; however had no significant effect on the lesion when given at 30 and 38 weeks. In addition, vitamin E supplemented at the ages from 6 to 30 weeks decreased the contents of serum oxLDL and TBARS without affecting the TC and TAG contents in serum and liver. Furthermore, vitamin E supplemented at 6, 14 and 22 weeks down-regulated vasculature mRNA expressions of scavenger receptor CD36 and up-regulated mRNA expressions of PPARγ, LXRα and ABCA1 which are involved in reverse cholesterol transportation; however had no significant effects on these genes when given at 30 and 38 weeks. In conclusion, vitamin E with same dose and duration inhibits the early but not advanced atherosclerotic lesion in ApoE KO mice by anti-oxidation and regulation of mRNA expression of genes involved in cholesterol uptake and efflux, which favors the improvement of atherosclerosis.

Indexed as

Age FactorsAnimalsAntioxidantsApolipoproteins EAtherosclerosisATP Binding Cassette Transporter 1CD36 AntigensCholesterolGene Expression RegulationLipoproteins, LDLLiverLiver X ReceptorsMaleMice, Inbred C57BLMice, KnockoutOrphan Nuclear ReceptorsAbca1 protein, mouseAntioxidantsApolipoproteins EATP Binding Cassette Transporter 1CD36 AntigensCholesterolLipoproteins, LDLLiver X ReceptorsNr1h3 protein, mouseOrphan Nuclear Receptorsoxidized low density lipoproteinPPAR gammaScavenger Receptors, Class AThiobarbituric Acid Reactive SubstancesVitamin E

Identifiers

PMID25385496
OpenAlexW2075536721

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.