Evidence map›Paper›PMID 17113194›Full record

ArticlePeptides2007

Enterostatin inhibition of dietary fat intake is modulated through the melanocortin system.

Ling Lin, Miejung Park, David A York

Abstract read
In one paragraph

Article in Peptides, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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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

3 authors at 2 institutions in 1 country.

Ling LinPennington Biomedical Research Center, Louisiana State University System, 6400 Perkins Road, Baton Rouge, LA 70808, USA.
Miejung Park
David A York
Louisiana State University System · USPennington Biomedical Research Center · US

Funding

ENTEROSTATIN REGULATION OF FAT INTAKER01DK045278 · NIDDK · UTAH STATE UNIVERSITY · PI YORK, DAVID A. · 1992 to 2005
$1.9M
NIDDK NIH HHS R01 DK045278-12NIDDK NIH HHS R01 DK045278-13PHS HHS NIDDK 4527
6 · The paper itself

Abstract

Enterostatin injected into the amygdala selectively reduces dietary fat intake by an action that involves a serotonergic component in the paraventricular nucleus. We have investigated the role of melanocortin signaling in the response to enterostatin by studies in melanocortin 4 receptor (MC4R) knock out mice and by the use of the MC4R and MC3R antagonist SHU9119, and by neurochemical phenotyping of enterostatin activated cells. We also determined the effect of enterostatin in vivo on the expression of AgRP in the hypothalamus and amygdala of rats and in culture on a GT1-7 neuronal cell line. Enterostatin had no effect on food intake in MC4R knock out mice. SHU9119 i.c.v. blocked the feeding response to amygdala enterostatin in rats. Amygdala enterostatin induced fos activation in alpha-melanocyte stimulating hormone (alpha-MSH) neurons in the arcuate nucleus. Enterostatin also reduced the expression of AgRP in the hypothalamus and amygdala and in GT1-7 cells. These data suggest enterostatin inhibits dietary fat intake through a melanocortin signaling pathway.

Indexed as

Agouti-Related Proteinalpha-MSHAmygdalaAnimalsArcuate Nucleus of HypothalamusBase SequenceCell LineColipasesDietary FatsDNA PrimersEatingEnzyme PrecursorsFemaleGene ExpressionHypothalamusIntercellular Signaling Peptides and ProteinsAgouti-Related Proteinalpha-MSHColipasesDietary FatsDNA PrimersEnzyme PrecursorsIntercellular Signaling Peptides and ProteinsMc3r protein, mouseMelanocyte-Stimulating HormonesprocolipasePro-OpiomelanocortinProtein PrecursorsReceptor, Melanocortin, Type 3Receptor, Melanocortin, Type 4SHU 9119

Identifiers

PMID17113194
PMCPMC1847607
OpenAlexW2054569491

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.