Evidence map›Paper›PMID 31447774›Full record

ArticleFrontiers in endocrinology2019

Increased Body Weight and Fat Mass After Subchronic GIP Receptor Antagonist, but Not GLP-2 Receptor Antagonist, Administration in Rats.

Sara Baldassano, Lærke Smidt Gasbjerg, Hüsün Sheyma Kizilkaya, Mette Marie Rosenkilde, Jens Juul Holst, Bolette Hartmann

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

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  19. Analysis of Body Perception, Preworkout Meal Habits and Bone Resorption in Child Gymnasts.International journal of environmental research and public health · 2021
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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

6 authors.

Sara BaldassanoDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Lærke Smidt GasbjergDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Hüsün Sheyma KizilkayaDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Mette Marie RosenkildeDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Jens Juul HolstDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
Bolette HartmannDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-2 (GLP-2) are hormones secreted from the enteroendocrine cells after a meal. They exert their actions through activation of G protein-coupled receptors (R), the GIPR and GLP-2R, respectively. Both have been reported to influence metabolism. The purpose of the study was to investigate the role of the hormones in the regulation of lipid and bone homeostasis by subchronic treatment with novel GIPR and GLP-2R antagonists. Rats were injected once daily with vehicle, GIPR, or GLP-2R antagonists for 3 weeks. Body weight, food intake, body composition, plasma lipoprotein lipase (LPL), adipokines, triglycerides and the marker of bone resorption carboxy-terminal collagen crosslinks (CTX), were examined. In rats, subchronic treatment with GIPR antagonist, rat GIP (3-30)NH

Indexed as

GIP receptorGIP receptor antagonistglucagon-like peptide-2 (GLP-2)glucose-dependent insulinotropic polypeptide (GIP)lipid homeostasis

Identifiers

PMID31447774
PMCPMC6691063

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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.