Evidence map›Paper›PMID 28533928›Full record

ArticleAmerican journal of cardiovascular disease2017

Leucine-nicotinic acid synergy stimulates AMPK/Sirt1 signaling and regulates lipid metabolism and lifespan in Caenorhabditis elegans, and hyperlipidemia and atherosclerosis in mice.

Antje Bruckbauer, Jheelam Banerjee, Quiang Cao, Xin Cui, Jia Jing, Lin Zha, Fenfen Li, Bingzhong Xue, Hang Shi, Michael B Zemel

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in American journal of cardiovascular disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Novel Role of the SIRT1 in Endocrine and Metabolic Diseases.International journal of biological sciences · 2023
    Review
  4. SIRT1 and thrombosis.Frontiers in molecular biosciences · 2023
    Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Antje BruckbauerNuSirt Biopharma Inc.Knoxville, TN, USA.
Jheelam BanerjeeNuSirt Biopharma Inc.Knoxville, TN, USA.
Quiang CaoCenter for Obesity Reversal, Georgia State UniversityAtlanta, GA, USA.
Xin CuiCenter for Obesity Reversal, Georgia State UniversityAtlanta, GA, USA.
Jia JingCenter for Obesity Reversal, Georgia State UniversityAtlanta, GA, USA.
Lin ZhaCenter for Obesity Reversal, Georgia State UniversityAtlanta, GA, USA.
Fenfen LiCenter for Obesity Reversal, Georgia State UniversityAtlanta, GA, USA.
Bingzhong XueCenter for Obesity Reversal, Georgia State UniversityAtlanta, GA, USA.
Hang ShiCenter for Obesity Reversal, Georgia State UniversityAtlanta, GA, USA.
Michael B ZemelNuSirt Biopharma Inc.Knoxville, TN, USA.
Georgia State University · USEpirus Biopharmaceuticals (United States) · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

BACKGROUND/

aimsNicotinic acid (NA), a lipid-lowering drug, serves as a source of NAD

methodsLDL-receptor knockout mice were fed an atherogenic Western diet supplemented with leucine (24 g/kg diet) and sub-therapeutic NA combinations (50 mg/kg diet and 250 mg/kg diet) or low therapeutic NA (1000 mg/kg diet) for 8 weeks to evaluate markers of hyperlipidemia and atherosclerosis.

resultsNA-Leu increased P-AMPK and Sirt1 in adipocytes and myotubes. In C. elegans, NA-Leu increased P-AMPK and DAF-16 (FOXO), reduced lipid accumulation and increased median survival under mild oxidative stress conditions. In the mice, NA-Leu reduced total cholesterol, cholesterol esters, plasma triglycerides, atherosclerotic lesion size, lipid area, and aortic macrophage infiltration, similar to the therapeutic NA dose.

conclusionLeu amplifies the effects of NA on lipid metabolism, hyperlipidemia and atherosclerosis in mice, at least in part by activation of the AMPK/Sirt1 axis. This combination may be a potential therapeutic alternative for hyperlipidemia and atherosclerosis.

Indexed as

AMPKatherosclerosisC. elegansleucinelipid metabolismnicotinic acidSirt1

Identifiers

PMID28533928
PMCPMC5435603
OpenAlexW2968410887

What Socratic 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 Socratic graph.