Evidence map›Paper›PMID 36251705›Full record

ArticlePloS one2022

The hypothalamic RFamide, QRFP, increases feeding and locomotor activity: The role of Gpr103 and orexin receptors.

Chris Cook, Nicolas Nunn, Amy A Worth, David A Bechtold, Todd Suter, Susan Gackeheimer, Lisa Foltz, Paul J Emmerson, Michael A Statnick, Simon M Luckman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

10 authors at 2 institutions in 2 countries.

Chris CookDivision of Diabetes, Endocrinology and Gastroenterology, School of Medicine, University of Manchester, Manchester, United Kingdom.
Nicolas NunnDivision of Diabetes, Endocrinology and Gastroenterology, School of Medicine, University of Manchester, Manchester, United Kingdom.
Amy A WorthDivision of Diabetes, Endocrinology and Gastroenterology, School of Medicine, University of Manchester, Manchester, United Kingdom.
David A BechtoldDivision of Diabetes, Endocrinology and Gastroenterology, School of Medicine, University of Manchester, Manchester, United Kingdom.
Todd SuterLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, United States of America.
Susan GackeheimerLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, United States of America.
Lisa FoltzLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, United States of America.
Paul J EmmersonLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, United States of America.
Michael A StatnickLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, United States of America.
Simon M LuckmanDivision of Diabetes, Endocrinology and Gastroenterology, School of Medicine, University of Manchester, Manchester, United Kingdom.ORCID 0000-0001-5318-5473
Eli Lilly (United States) · USUniversity of Manchester · GB

Funding

Biotechnology and Biological Sciences Research Council BB/J005509/1Biotechnology and Biological Sciences Research Council BB/R003858/1
6 · The paper itself

Abstract

Here we show that central administration of pyroglutamylated arginine-phenylamine-amide peptide (QRFP/26RFa) increases both food intake and locomotor activity, without any significant effect on energy expenditure, thermogenesis or reward. Germline knock out of either of the mouse QRFP receptor orthologs, Gpr103a and Gpr103b, did not produce a metabolic phenotype. However, both receptors are required for the effect of centrally administered QRFP to increase feeding and locomotor activity. As central injection of QRFP activated orexin/hypocretin neurons in the lateral hypothalamus, we compared the action of QRFP and orexin on behaviour. Both peptides increased arousal and locomotor activity. However, while orexin increased consummatory behaviour, QRFP also affected other appetitive behaviours. Furthermore, the feeding but not the locomotor response to QRFP, was blocked by co-administration of an orexin receptor 1 antagonist. These results suggest that QRFP agonism induces both appetitive and consummatory behaviour, but only the latter is dependent on orexin/hypocretin receptor signalling.

Indexed as

Orexin ReceptorsPeptidesReceptors, G-Protein-CoupledAmidesAniline CompoundsAnimalsArginineFeeding BehaviorIntercellular Signaling Peptides and ProteinsLocomotionMiceNeuropeptidesOrexinsAmidesAniline CompoundsArgininearginylphenylalaninamideIntercellular Signaling Peptides and ProteinsNeuropeptidesOrexin ReceptorsOrexinsPeptidesQrfpr protein, mouseReceptors, G-Protein-Coupled

Identifiers

PMID36251705
PMCPMC9576062
OpenAlexW4306632316

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.