Evidence map›Paper›PMID 35813647›Full record

ArticleFrontiers in endocrinology2022

Metabolic Stress Impairs Pericyte Response to Optogenetic Stimulation in Pancreatic Islets.

Aurélien Michau, Chrystel Lafont, Paula Bargi-Souza, Yasmine Kemkem, Anne Guillou, Magalie A Ravier, Gyslaine Bertrand, Annie Varrault, Tatiana Fiordelisio, David J Hodson and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2022. 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
1.5field-weighted citation impact, top 18% 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, 7 citations in OpenAlex.

  1. Review
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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

12 authors at 5 institutions in 4 countries.

Aurélien MichauInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Chrystel LafontInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Paula Bargi-SouzaInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Yasmine KemkemInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Anne GuillouInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Magalie A RavierInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Gyslaine BertrandInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Annie VarraultInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Tatiana FiordelisioInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
David J HodsonOxford Centre for Diabetes, Endocrinology and Metabolism (OCDEM), National Institute for Health and Care Research (NIHR) Oxford Biomedical Research Centre, Churchill Hospital, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Patrice MollardInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Marie SchaefferInstitute of Functional Genomics, Univ. Montpellier, CNRS, INSERM, Montpellier, France.
Institut de Génomique Fonctionnelle · FRCentre National de la Recherche Scientifique · FRInserm · FRCentre de Biologie Structurale · FROxford Centre for Diabetes, Endocrinology and Metabolism · GB

Funding

Medical Research Council MR/N00275X/1Medical Research Council MR/S025618/1
6 · The paper itself

Abstract

Pancreatic islets are highly vascularized micro-organs ensuring whole body glucose homeostasis. Islet vascular cells play an integral part in sustaining adequate insulin release by beta cells. In particular, recent studies have demonstrated that islet pericytes regulate local blood flow velocity and are required for maintenance of beta cell maturity and function. In addition, increased metabolic demand accompanying obesity alters islet pericyte morphology. Here, we sought to explore the effects of metabolic stress on islet pericyte functional response to stimulation in a mouse model of type 2 diabetes, directly in the pancreas

Indexed as

Diabetes Mellitus, Type 2Islets of LangerhansAnimalsMiceOptogeneticsPericytesStress, Physiologicaldiabetesimagingin vivooptogeneticspancreaspericytevessel

Identifiers

PMID35813647
PMCPMC9259887
OpenAlexW4283328161

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.