Evidence map›Paper›PMID 27530231›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2016

Central GIP signaling stimulates peripheral GIP release and promotes insulin and pancreatic polypeptide secretion in nonhuman primates.

Paul B Higgins, Robert E Shade, Irám P Rodríguez-Sánchez, Magdalena Garcia-Forey, M Elizabeth Tejero, V Saroja Voruganti, Shelley A Cole, Anthony G Comuzzie, Franco Folli

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  5. Incretin secretion in humans is under the influence of cannabinoid receptors.American journal of physiology. Endocrinology and metabolism · 2017
    Observational
  6. Article
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

9 authors at 5 institutions in 4 countries.

Paul B HigginsDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, Texas; Southwest National Primate Research Center, San Antonio, Texas; paulb.higgins@gmail.com.
Robert E ShadeSouthwest National Primate Research Center, San Antonio, Texas.
Irám P Rodríguez-SánchezDepartment of Genetics, School of Medicine, Autonomous University of Nuevo León (Universidad Autonoma de Nuevo León), Monterrey, Nuevo León, Mexico.
Magdalena Garcia-ForeySouthwest National Primate Research Center, San Antonio, Texas.
M Elizabeth TejeroLaboratory of Nutrigenetics and Nutrigenomics, National Institute of Genomic Medicine (Instituto Nacional de Medicina Genómica), Mexico City, Mexico.
V Saroja VorugantiDepartment of Nutrition and UNC Nutrition Research Institute, University of North Carolina at Chapel Hill, Kannapolis, North Carolina.
Shelley A ColeDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, Texas.
Anthony G ComuzzieDepartment of Genetics, Texas Biomedical Research Institute, San Antonio, Texas; Southwest National Primate Research Center, San Antonio, Texas.
Franco FolliSouthwest National Primate Research Center, San Antonio, Texas; Diabetes Division, Department of Medicine, University of Texas Health Sciences Center at San Antonio, San Antonio, Texas; Department of Medicine, Obesity and Comorbidities Research Center, University of Campinas, Campinas, São Paulo, Brazil; and Dipartimento di Scienze della Salute, Università degli Studi di Milano, Milan, Italy.
Texas Biomedical Research Institute · USNational Institute of Genomic Medicine · MXThe University of Texas Health Science Center at San Antonio · USUniversidad Autónoma de Nuevo León · MXUniversity of North Carolina at Chapel Hill · US

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
NIH HHS P51 OD011133
6 · The paper itself

Abstract

Glucose-dependent insulinotropic polypeptide (GIP) has important actions on whole body metabolic function. GIP and its receptor are also present in the central nervous system and have been linked to neurotrophic actions. Metabolic effects of central nervous system GIP signaling have not been reported. We investigated whether centrally administered GIP could increase peripheral plasma GIP concentrations and influence the metabolic response to a mixed macronutrient meal in nonhuman primates. An infusion and sampling system was developed to enable continuous intracerebroventricular (ICV) infusions with serial venous sampling in conscious nonhuman primates. Male baboons (Papio sp.) that were healthy and had normal body weights (28.9 ± 2.1 kg) were studied (n = 3). Animals were randomized to receive continuous ICV infusions of GIP (20 pmol·kg

Indexed as

AnimalsBlood GlucoseEatingGastric Inhibitory PolypeptideInfusions, IntraventricularInsulinMalePancreatic PolypeptidePancreatic Polypeptide-Secreting CellsPapioPostprandial PeriodSpecies SpecificityStereotaxic TechniquesBlood GlucoseGastric Inhibitory PolypeptideInsulinPancreatic Polypeptidebrainglucose-dependent insulinotropic polypeptideintracerebroventricularnonhuman primate

Identifiers

PMID27530231
PMCPMC5241561
OpenAlexW2507881376

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.