Evidence mapPaperPMID 39703141Full record

ArticleAdvanced biology2025

Enteroendocrine Cells Sense Sucrose and Alter Enteric Neuron Excitability via Insulin Signaling.

Jessica R Snyder, Minhal Ahmed, Sukhada Bhave, Ryo Hotta, Ryan A Koppes, Allan M Goldstein, Abigail N Koppes

Abstract read
In one paragraph

Article in Advanced biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Jessica R SnyderDepartment of Bioengineering, Northeastern University, 360 Huntington Ave, Boston, MA, 02115, USA.ORCID https://orcid.org/0009-0000-4646-1249
Minhal AhmedHarvard Medical School, 25 Shattuck St, Boston, MA, 02115, USA.ORCID https://orcid.org/0000-0001-5347-8524
Sukhada BhaveDepartment of Pediatric Surgery, Massachusetts General Hospital, Harvard Medical School, 55 Fruit Street, 185 Cambridge St, CPZN 6-215, Boston, MA, 02114, USA.
Ryo HottaDepartment of Pediatric Surgery, Massachusetts General Hospital, Harvard Medical School, 55 Fruit Street, 185 Cambridge St, CPZN 6-215, Boston, MA, 02114, USA.ORCID https://orcid.org/0000-0001-9890-8241
Ryan A KoppesDepartment of Chemical Engineering, Northeastern University, 360 Huntington Ave, Boston, MA, 02115, USA.ORCID https://orcid.org/0000-0002-3376-6358
Allan M GoldsteinDepartment of Pediatric Surgery, Massachusetts General Hospital, Harvard Medical School, 55 Fruit Street, 185 Cambridge St, CPZN 6-215, Boston, MA, 02114, USA.ORCID https://orcid.org/0000-0003-2106-847X
Abigail N KoppesDepartment of Bioengineering, Northeastern University, 360 Huntington Ave, Boston, MA, 02115, USA.ORCID https://orcid.org/0000-0003-0433-9290

Funding

Engineering multifaceted 3D human organ platforms for toxicity testingR35GM142741 · NORTHEASTERN UNIVERSITY · 2025 to 2025
$393k
Division of Chemical, Bioengineering, Environmental, and Transport Systems 2045906NIGMS NIH HHS R35 GM142741
6 · The paper itself

Abstract

Neurosensory circuits of the gastrointestinal tract sense microbial and nutrient changes in the gut; however, studying these circuits in vivo is hindered by invasive techniques and ethical concerns. Here, an in vitro model of enteroendocrine cells (EECs) and calcium reporting enteric neurons (ENs) is established and validated for functional signaling. Both mechanical and sucrose stimulation of co-cultures increased the percentage of neurons undergoing a calcium flux, indicating an action potential. Neuronal activation is blocked with either a piezo or insulin receptor blocker. At baseline, a flow only stimulus elicited 51.9% of neurons to activate in co-culture, which is decreased to 15.1% with a piezo blocker. Piezo blocked and sucrose stimulated EECs increased neuronal activation to 43.9%, and an insulin blocker reduced response to 12.4%. Since a cell line is used to model the EEC in the previous experiments, primary rat duodenal epithelium enriched for EECs are also stimulated and found to produced measurable insulin. This work shows the ability of EECs to produce insulin and for ENs to sense insulin. These results inspire further work on how insulin production outside the pancreas effects diabetes, insulin as a neurotransmitter, and exploration of additional nutritional and microbiotic stimuli on enteroendocrine-to-neuronal signaling.

Indexed as

Enteric Nervous SystemEnteroendocrine CellsInsulinNeuronsSucroseAction PotentialsAnimalsCells, CulturedCoculture TechniquesRatsRats, Sprague-DawleySignal TransductionInsulinSucroseenteric nervous systementeroendocrine cellsinsulinmicrophysiological systemorgan‐chip

Identifiers

PMID39703141
PMCPMC11913573

What Socratic holds

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Registered trials

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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 Socratic graph.