Evidence map›Paper›PMID 27683551›Full record

ArticleScience translational medicine2016

Prevention of atherosclerosis by bioactive palmitoleate through suppression of organelle stress and inflammasome activation.

Ismail Çimen, Begüm Kocatürk, Seda Koyuncu, Özlem Tufanlı, Umut I Onat, Asli D Yıldırım, Onur Apaydın, Şeyma Demirsoy, Zaliha G Aykut, Uyen T Nguyen and 3 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Science translational medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05560971 (The Effect of Palmitoleic Acid), which is not on this map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
11.9field-weighted citation impact, top 1% 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.

NCT05560971 naactive not recruitingnot on this mapstarted 2022, after this paper: background citation

The Effect of Palmitoleic Acid (POA) Supplementation on Insulin Sensitivity and Lipogenesis in Overweight and Obese Individuals

TypeinterventionalSponsorBrigham and Women's HospitalRan2022 to 2027Enrolled40ConditionsPreDiabetes, Insulin Resistance, Overweight, ObesityArmsPalmitoleic acid, Placebo
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 101 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Crosstalk Between Adipose Tissue and the Heart: An Update.Journal of translational internal medicine · 2022
    Article
  13. Review
  14. Article
  15. Review
  16. Novel Adipose Tissue Targets to Prevent and Treat Atherosclerosis.Handbook of experimental pharmacology · 2022
    Article
  17. Article
  18. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Ismail ÇimenDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey. National Nanotechnology Research Center, Bilkent University, Ankara 06800, Turkey.
Begüm KocatürkDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey. National Nanotechnology Research Center, Bilkent University, Ankara 06800, Turkey.
Seda KoyuncuDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey.
Özlem TufanlıDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey. National Nanotechnology Research Center, Bilkent University, Ankara 06800, Turkey.
Umut I OnatDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey. National Nanotechnology Research Center, Bilkent University, Ankara 06800, Turkey.
Asli D YıldırımDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey. National Nanotechnology Research Center, Bilkent University, Ankara 06800, Turkey.
Onur ApaydınDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey. National Nanotechnology Research Center, Bilkent University, Ankara 06800, Turkey.
Şeyma DemirsoyDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey.
Zaliha G AykutDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey.
Uyen T NguyenMetabolon, Sacramento, CA 95691, USA.
Steven M WatkinsMetabolon, Sacramento, CA 95691, USA.
Gökhan S HotamışlıgilDepartment of Genetics and Complex Diseases and Sabri Ülker Center, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA.
Ebru ErbayDepartment of Molecular Biology and Genetics, Bilkent University, Ankara 06800, Turkey. National Nanotechnology Research Center, Bilkent University, Ankara 06800, Turkey. eerbay@bilkent.edu.tr.
Bilkent University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

De novo lipogenesis (DNL), the conversion of glucose and other substrates to lipids, is often associated with ectopic lipid accumulation, metabolic stress, and insulin resistance, especially in the liver. However, organ-specific DNL can also generate distinct lipids with beneficial metabolic bioactivity, prompting a great interest in their use for the treatment of metabolic diseases. Palmitoleate (PAO), one such bioactive lipid, regulates lipid metabolism in liver and improves glucose utilization in skeletal muscle when it is generated de novo from the obese adipose tissue. We show that PAO treatment evokes an overall lipidomic remodeling of the endoplasmic reticulum (ER) membranes in macrophages and mouse tissues, which is associated with resistance of the ER to hyperlipidemic stress. By preventing ER stress, PAO blocks lipid-induced inflammasome activation in mouse and human macrophages. Chronic PAO supplementation also lowers systemic interleukin-1β (IL-1β) and IL-18 concentrations in vivo in hyperlipidemic mice. Moreover, PAO prevents macrophage ER stress and IL-1β production in atherosclerotic plaques in vivo, resulting in a marked reduction in plaque macrophages and protection against atherosclerosis in mice. These findings demonstrate that oral supplementation with a product of DNL such as PAO can promote membrane remodeling associated with metabolic resilience of intracellular organelles to lipid stress and limit the progression of atherosclerosis. These findings support therapeutic PAO supplementation as a potential preventive approach against complex metabolic and inflammatory diseases such as atherosclerosis, which warrants further studies in humans.

Indexed as

AnimalsApolipoproteins EApoptosisAtherosclerosisCells, CulturedCytokinesEndoplasmic ReticulumEndoplasmic Reticulum StressFatty Acids, MonounsaturatedInflammasomesInflammationInflammation MediatorsIntracellular MembranesLipidsMacrophagesMiceApolipoproteins ECytokinesFatty Acids, MonounsaturatedInflammasomesInflammation MediatorsLipidspalmitoleic acid

Identifiers

PMID27683551
OpenAlexW2524755859

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.