Evidence map›Paper›PMID 24879927›Full record

ArticlePeptides2014

Differences in acute anorectic effects of long-acting GLP-1 receptor agonists in rats.

Stephanie Sisley, Kathleen Smith, Darleen A Sandoval, Randy J Seeley

Open access · greenAbstract read
In one paragraph

Article in Peptides, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.4field-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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  3. Article
  4. Article
  5. Review
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  9. Article
  10. Brain GLP-1 and insulin sensitivity.Molecular and cellular endocrinology · 2015
    Review
  11. Article
  12. Article
  13. Liraglutide and obesity: a review of the data so far.Drug design, development and therapy · 2015
    Review
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

4 authors at 2 institutions in 1 country.

Stephanie SisleyDepartment of Pediatrics, Division of Endocrinology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States. Electronic address: Stephanie.sisley@bcm.edu.
Kathleen SmithDepartment of Internal Medicine, Division of Endocrinology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Darleen A SandovalDepartment of Internal Medicine, Division of Endocrinology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Randy J SeeleyDepartment of Internal Medicine, Division of Endocrinology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
University of Cincinnati Medical Center · USCincinnati Children's Hospital Medical Center · US

Funding

Role of Glucokinase in GLP-1 Regulation of Energy and Glucose HomeostasisR01DK082480 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SANDOVAL, DARLEEN A. · 2010 to 2014
$1.7M
Dissecting mechanisms of GLP-1 based therapies for Type II DiabetesR01DK093848 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SEELEY, RANDY J · 2012 to 2015
$1.5M
CNS NFkappaB Regulation of Glucose HomeostasisF32DK091077 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI SISLEY, STEPHANIE RENEE · 2011 to 2012
$86k
NIDDK NIH HHS 1F32DK091077-01A1NIDDK NIH HHS DK082480NIDDK NIH HHS DK093848NIDDK NIH HHS F32 DK091077NIDDK NIH HHS R01 DK082480NIDDK NIH HHS R01 DK093848
6 · The paper itself

Abstract

Long-acting glucagon-like peptide-1 receptor (GLP-1R) agonists have both glucose- and weight-lowering effects. The brain is poised to mediate both of these actions since GLP-1Rs are present in key areas known to control weight and glucose. Although some research has been performed on the effects of exendin-4 in the brain, little data exists on the central effects of liraglutide, a long-acting GLP-1R agonist with much closer structural homology to native GLP-1. In lean, Long-Evans rats, we found that direct intra-third cerebroventricular (i3vt) administration of 0.26 nmol liraglutide caused a 50% reduction in food intake. However, exendin-4 produced the same reduction in food intake with 10-fold greater potency (0.02 nmol). These data are supported by similar c-Fos immunoreactivity in the hypothalamic paraventricular nuclei by exendin-4 as compared to liraglutide despite differing doses. The anorectic effects of both drugs were blocked with i3vt pre-treatment of a GLP-1R competitive antagonist, exendin(9-39), indicating that both drugs required the GLP-1R for their effects. Exendin-4, and not liraglutide, caused hyperglycemia when given i3vt prior to an oral glucose tolerance test, although liraglutide did not lower glucose. Thus, these data show that GLP-1R agonists have differing anorectic potencies in the CNS, which may account for some of their clinical differences. Additionally, we show here that the glucose lowering properties of acute administration of GLP-1R agonists are not accounted for by their central effects.

Indexed as

AnimalsAnorexiaEatingExenatideGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorHyperglycemiaHypoglycemic AgentsHypothalamusLiraglutideMalePeptidesRatsRats, Long-EvansReceptors, GlucagonVenomsExenatideGlp1r protein, ratGlucagon-Like Peptide 1Glucagon-Like Peptide-1 ReceptorHypoglycemic AgentsLiraglutidePeptidesReceptors, GlucagonVenomsBrainExendin-4GLP-1RLiraglutide

Identifiers

PMID24879927
PMCPMC4113007
OpenAlexW2013998327

What OpenQuestion holds

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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.