Evidence map›Paper›PMID 27229177›Full record

ArticleScientific reports2016

NAMPT knockdown attenuates atherosclerosis and promotes reverse cholesterol transport in ApoE KO mice with high-fat-induced insulin resistance.

Shengbing Li, Cong Wang, Ke Li, Ling Li, Mingyuan Tian, Jing Xie, Mengliu Yang, Yanjun Jia, Junying He, Lin Gao and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Targeted NADJournal of controlled release : official journal of the Controlled Release Society · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Role of post-translational modifications of Sp1 in cardiovascular diseases.Frontiers in cell and developmental biology · 2024
    Review
  8. Article
  9. Adipokines, adiposity, and atherosclerosis.Cellular and molecular life sciences : CMLS · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. 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

13 authors at 6 institutions in 2 countries.

Shengbing LiDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Cong WangDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Ke LiDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Ling LiThe Key Laboratory of Laboratory Medical Diagnostics in the Ministry of Education and Department of Clinical Biochemistry, College of Laboratory Medicine, Chongqing Medical University, 400010 Chongqing, China.
Mingyuan TianDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Jing XieDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Mengliu YangDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Yanjun JiaDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Junying HeDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Lin GaoDepartment of Endocrinology, the Affiliated Hospital, Zunyi Medical College, 563003 Guizhou, China.
Guenther BodenThe Division of Endocrinology/Diabetes/Metabolism and the Clinical Research Center, Temple University School of Medicine, Philadelphia, Pennsylvania, USA.
Hua LiuDepartment of Pediatrics, University of Mississippi Medical Center, 2500 North State Street, Jackson, Mississippi, MS 39216-4505, USA.
Gangyi YangDepartment of Endocrinology, the Second Affiliated Hospital, Chongqing Medical University, 400010 Chongqing, China.
Second Affiliated Hospital of Chongqing Medical University · CNDalian Medical University · CNAffiliated Hospital of Zunyi Medical College · CNChongqing Medical University · CNTemple University · USUniversity of Mississippi Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NAMPT has been suggested association with atherosclerosis and insulin resistance. However, the impact of NAMPT on atherosclerosis remained unknown. Therefore, the objective of this study was to use a NAMPT loss-of-function approach to investigate the effect of NAMPT on atherosclerosis in hypercholesterolemic mice. We demonstrated that a specific NAMPT knockdown increased plasma HDL-C levels, reduced the plaque area of the total aorta en face and the cross-sectional aortic sinus, decreased macrophage number and apoptosis, and promoted RCT in HFD-fed ApoE KO mice. These changes were accompanied by increased PPARα, LXRα, ABCA1 and ABCG1 expressions in the liver. NAMPT knockdown also facilitated cholesterol efflux in RAW264.7 cells. We further investigated the effect of NAMPT knockdown on the PPARα-LXRα pathway of cholesterol metabolism with MK886 (a selective inhibitor of PPARα) in RAW264.7 macrophages. MK886 abolished the ability of NAMPT knockdown to decrease intracellular cholesterol levels to enhance the rate of (3)H-cholesterol efflux and to increase ABCA1/G1 and LXRα expressions in RAW264.7 macrophages. Our observations demonstrate that NAMPT knockdown exerted antiatherogenic effects by promoting cholesterol efflux and macrophage RCT through the PPARα- LXRα- ABCA1/G1pathway in vitro and in vivo.

Indexed as

AtherosclerosisInsulin ResistanceAnimalsApolipoproteins ECholesterol, HDLCytokinesDietary FatsGene Knockdown TechniquesMaleMiceMice, KnockoutNicotinamide PhosphoribosyltransferaseRAW 264.7 CellsApolipoproteins ECholesterol, HDLCytokinesDietary FatsNicotinamide Phosphoribosyltransferasenicotinamide phosphoribosyltransferase, mouse

Identifiers

PMID27229177
PMCPMC4882618
OpenAlexW2407226919

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.