Evidence map›Paper›PMID 25028498›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2014

Insulin-like peptide 5 is an orexigenic gastrointestinal hormone.

Johannes Grosse, Helen Heffron, Keith Burling, Mohammed Akhter Hossain, Abdella M Habib, Gareth J Rogers, Paul Richards, Rachel Larder, Debra Rimmington, Alice A Adriaenssens and 13 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 1 pooled it
7.1field-weighted citation impact, top 2% 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

73 citing papers in PubMed, 1 synthesis or guideline pooled it, 146 citations in OpenAlex.

  1. Pooled it
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  14. Effects of dietary fibre on metabolic health and obesity.Nature reviews. Gastroenterology & hepatology · 2024
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13 more citing papers are in PubMed but not listed here.

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

23 authors at 7 institutions in 4 countries.

Johannes GrosseTakeda Cambridge Ltd., Cambridge CB4 0PA, United Kingdom;
Helen HeffronTakeda Cambridge Ltd., Cambridge CB4 0PA, United Kingdom;
Keith BurlingCore Biochemical Assay Laboratory, Addenbrooke's Hospital, Cambridge CB2 0QQ, United Kingdom;
Mohammed Akhter HossainFlorey Institute of Neuroscience and Mental Health, and School of Chemistry, University of Melbourne, Melbourne, VIC 3010, Australia;
Abdella M HabibCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom;
Gareth J RogersCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom;
Paul RichardsCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom;Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, United Kingdom;
Rachel LarderMetabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, United Kingdom;
Debra RimmingtonMetabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, United Kingdom;
Alice A AdriaenssensCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom;Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, United Kingdom;
Laura PartonTakeda Cambridge Ltd., Cambridge CB4 0PA, United Kingdom;
Justin PowellTakeda Cambridge Ltd., Cambridge CB4 0PA, United Kingdom;
Matteo BindaFrimorfo Ltd., 1723 Fribourg, Switzerland;
William H ColledgeDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, United Kingdom;
Joanne DoranTakeda Cambridge Ltd., Cambridge CB4 0PA, United Kingdom;
Yukio ToyodaTakeda Pharmaceutical Co. Ltd., Osaka, Japan; and.
John D WadeFlorey Institute of Neuroscience and Mental Health, and School of Chemistry, University of Melbourne, Melbourne, VIC 3010, Australia;
Samuel AparicioBritish Columbia Cancer Agency Branch, Vancouver, Canada V5Z 1L3.
Mark B L CarltonTakeda Cambridge Ltd., Cambridge CB4 0PA, United Kingdom;
Anthony P CollMetabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, United Kingdom;
Frank ReimannCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom;Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, United Kingdom;
Stephen O'RahillyMetabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, United Kingdom; so104@medschl.cam.ac.uk.
Fiona M GribbleCambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, United Kingdom;Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Institute of Metabolic Science, University of Cambridge, Cambridge CB2 0QQ, United Kingdom;
Takeda (United Kingdom) · GBUniversity of Cambridge · GBWellcome/MRC Institute of Metabolic Science · GBUniversity of Melbourne · AUAddenbrooke's Hospital · GBBC Cancer Agency · CATakeda (Japan) · JP

Funding

Medical Research Council 4050281695Medical Research Council G0600717Medical Research Council G0900554Medical Research Council G9824984Medical Research Council MC_UU_12012/1Medical Research Council MC_UU_12012/3Medical Research Council MC_UU_12012/5Wellcome Trust 084210Wellcome Trust 088357Wellcome Trust 095515Wellcome Trust 100574
6 · The paper itself

Abstract

The gut endocrine system is emerging as a central player in the control of appetite and glucose homeostasis, and as a rich source of peptides with therapeutic potential in the field of diabetes and obesity. In this study we have explored the physiology of insulin-like peptide 5 (Insl5), which we identified as a product of colonic enteroendocrine L-cells, better known for their secretion of glucagon-like peptide-1 and peptideYY. i.p. Insl5 increased food intake in wild-type mice but not mice lacking the cognate receptor Rxfp4. Plasma Insl5 levels were elevated by fasting or prolonged calorie restriction, and declined with feeding. We conclude that Insl5 is an orexigenic hormone released from colonic L-cells, which promotes appetite during conditions of energy deprivation.

Indexed as

AnimalsColonEatingEnteroendocrine CellsFemaleGlucagon-Like Peptide 1HumansMaleMiceMice, KnockoutPeptide HormonesPeptide YYReceptors, G-Protein-CoupledReceptors, PeptideGlucagon-Like Peptide 1Insl5 protein, mousePeptide HormonesPeptide YYReceptors, G-Protein-CoupledReceptors, PeptideRXFP4 protein, humanRXFP4 protein, mouse

Identifiers

PMID25028498
PMCPMC4121845
OpenAlexW2004827855

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.