Evidence map›Paper›PMID 20628144›Full record

ArticleJournal of lipid research2010

Glucose regulates fatty acid binding protein interaction with lipids and peroxisome proliferator-activated receptor α.

Heather A Hostetler, Madhumitha Balanarasimha, Huan Huang, Matthew S Kelzer, Alagammai Kaliappan, Ann B Kier, Friedhelm Schroeder

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
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  5. Impact ofJournal of lipid research · 2017
    Article
  6. Article
  7. Review
  8. Article
  9. Impact of SCP-2/SCP-x gene ablation and dietary cholesterol on hepatic lipid accumulation.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Article
  10. Review
  11. Human FABP1 T94A variant impacts fatty acid metabolism and PPAR-α activation in cultured human female hepatocytes.American journal of physiology. Gastrointestinal and liver physiology · 2014
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Impact of L-FABP and glucose on polyunsaturated fatty acid induction of PPARα-regulated β-oxidative enzymes.American journal of physiology. Gastrointestinal and liver physiology · 2013
    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.

Heather A HostetlerDepartments of Physiology and Pharmacology, Texas A&M University, TVMC, College Station, TX, USA.
Madhumitha Balanarasimha
Huan Huang
Matthew S Kelzer
Alagammai Kaliappan
Ann B Kier
Friedhelm Schroeder
Wright State University · USTexas A&M University · US

Funding

FATTY ACID BINDING PROTEINS-LIGAND SPECIFICITYR01DK041402 · NIDDK · UNIVERSITY OF CINCINNATI · PI SCHROEDER, FRIEDHELM · 1989 to 2010
$4.4M
The role of long chain acyl-CoAs in nuclear receptor regulationR00DK077573 · NIDDK · WRIGHT STATE UNIVERSITY · PI HOSTETLER, HEATHER A · 2009 to 2011
$747k
The role of long chain acyl-CoAs in nuclear receptor regulationK99DK077573 · NIDDK · TEXAS A&M AGRILIFE RESEARCH · PI HOSTETLER, HEATHER A · 2007 to 2008
$179k
NIDDK NIH HHS DK-41402NIDDK NIH HHS DK-77573NIDDK NIH HHS K99 DK077573NIDDK NIH HHS R00 DK077573NIDDK NIH HHS R01 DK041402
6 · The paper itself

Abstract

Although the pathophysiology of diabetes is characterized by elevated levels of glucose and long-chain fatty acids (LCFA), nuclear mechanisms linking glucose and LCFA metabolism are poorly understood. As the liver fatty acid binding protein (L-FABP) shuttles LCFA to the nucleus, where L-FABP directly interacts with peroxisome proliferator-activated receptor-α (PPARα), the effect of glucose on these processes was examined. In vitro studies showed that L-FABP strongly bound glucose and glucose-1-phosphate (K(d) = 103 ± 19 nM and K(d) = 20 ± 3 nM, respectively), resulting in altered L-FABP conformation, increased affinity for lipid ligands, and enhanced interaction with PPARα. In living cells, glucose stimulated cellular uptake and nuclear localization of a nonmetabolizable fluorescent fatty acid analog (BODIPY C-16), particularly in the presence of L-FABP. These data suggest for the first time a direct role of glucose in facilitating L-FABP-mediated uptake and distribution of lipidic ligands to the nucleus for regulation of PPARα transcriptional activity.

Indexed as

Active Transport, Cell NucleusAnimalsCell NucleusCells, CulturedDose-Response Relationship, DrugFatty Acid-Binding ProteinsFatty AcidsGlucoseLipid MetabolismMicePPAR alphaProtein BindingProtein Structure, SecondaryRatsFatty Acid-Binding ProteinsFatty AcidsGlucosePPAR alpha

Identifiers

PMID20628144
PMCPMC2952551
OpenAlexW2015759207

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.