Evidence map›Paper›PMID 29782847›Full record

ArticleGastroenterology2018

Optogenetic Induction of Colonic Motility in Mice.

Timothy J Hibberd, Jing Feng, Jialie Luo, Pu Yang, Vijay K Samineni, Robert W Gereau, Nigel Kelley, Hongzhen Hu, Nick J Spencer

Open access · greenAbstract read
In one paragraph

Article in Gastroenterology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 5% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

  1. Optogenetic control of the enteric nervous system and gastrointestinal transit.Expert review of gastroenterology & hepatology · 2019
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Direct Stimulation of Gastric Smooth Muscle Cells via GNeurogastroenterology and motility · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Unique properties of proximal and distal colon reflect distinct motor functions.American journal of physiology. Gastrointestinal and liver physiology · 2025
    Review
  10. Insights Into Gastrointestinal Motility Through the Use of Optogenetic Sensors.Journal of neurogastroenterology and motility · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. The enteric nervous system.Physiological reviews · 2023
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Timothy J HibberdCollege of Medicine and Public Health and Centre for Neuroscience, Flinders University, Adelaide, Australia.
Jing FengDepartment of Anesthesiology, The Center for the Study of Itch, Washington University School of Medicine, St Louis, Missouri.
Jialie LuoDepartment of Anesthesiology, The Center for the Study of Itch, Washington University School of Medicine, St Louis, Missouri.
Pu YangDepartment of Anesthesiology, The Center for the Study of Itch, Washington University School of Medicine, St Louis, Missouri.
Vijay K SamineniWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine, St Louis, Missouri.
Robert W GereauWashington University Pain Center, Department of Anesthesiology, Washington University School of Medicine, St Louis, Missouri.
Nigel KelleySA Biomedical Engineering, SA Health, Government of South Australia, Adelaide, Australia.
Hongzhen HuDepartment of Anesthesiology, The Center for the Study of Itch, Washington University School of Medicine, St Louis, Missouri. Electronic address: hongzhen.hu@wustl.edu.
Nick J SpencerCollege of Medicine and Public Health and Centre for Neuroscience, Flinders University, Adelaide, Australia. Electronic address: nicholas.spencer@flinders.edu.au.
Washington University in St. Louis · USFlinders University · AUGovernment of South Australia · AU

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
Multimodal biocompatible microLED devices for diverse neuroscience applicationsR01NS081707 · NINDS · WASHINGTON UNIVERSITY · PI GEREAU, ROBERT W, ROGERS, JOHN · 2012 to 2016
$3.9M
TARGETING THE TRANSIENT RECEPTOR POTENTIAL CHANNELS TO IMPROVE BOWEL DYSFUNCTIONR01DK103901 · NIDDK · WASHINGTON UNIVERSITY · PI HU, HONGZHEN · 2015 to 2023
$3.4M
Mechanisms of Zinc Regulation of Pain-initiating TRP ChannelsR01GM101218 · NIGMS · WASHINGTON UNIVERSITY · PI HU, HONGZHEN · 2013 to 2017
$1.4M
Soft, conformal wireless optoelectronic systems for the long-term neuromodulation of bladder functionU18EB021793 · NIBIB · WASHINGTON UNIVERSITY · PI GEREAU, ROBERT W, ROGERS, JOHN · 2015 to 2018
$877k
NIBIB NIH HHS U18 EB021793NIDDK NIH HHS P30 DK052574NIDDK NIH HHS R01 DK103901NIGMS NIH HHS R01 GM101218NINDS NIH HHS R01 NS081707
6 · The paper itself

Abstract

BACKGROUND &

aimsStrategies are needed to increase gastrointestinal transit without systemic pharmacologic agents. We investigated whether optogenetics, focal application of light to control enteric nervous system excitability, could be used to evoke propagating contractions and increase colonic transit in mice.

methodsWe generated transgenic mice with Cre-mediated expression of light-sensitive channelrhodopsin-2 (ChR2) in calretinin neurons (CAL-ChR2 Cre+ mice); Cre- littermates served as controls. Colonic myenteric neurons were analyzed by immunohistochemistry, patch-clamp, and calcium imaging studies. Motility was assessed by mechanical, electrophysiological, and video recording in vitro and by fecal output in vivo.

resultsIn isolated colons, focal light stimulation of calretinin enteric neurons evoked classic polarized motor reflexes (50/58 stimulations), followed by premature anterograde propagating contractions (39/58 stimulations). Light stimulation could evoke motility from sites along the entire colon. These effects were prevented by neural blockade with tetrodotoxin (n = 2), and did not occur in control mice (n = 5). Light stimulation of proximal colon increased the proportion of natural fecal pellets expelled over 15 minutes in vitro (75% ± 17% vs 32% ± 8% for controls) (P < .05). In vivo, activation of wireless light-emitting diodes implanted onto the colon wall significantly increased hourly fecal pellet output in conscious, freely moving mice (4.2 ± 0.4 vs 1.3 ± 0.3 in controls) (P < .001).

conclusionsIn studies of mice, we found that focal activation of a subset of enteric neurons can increase motility of the entire colon in vitro, and fecal output in vivo. Optogenetic control of enteric neurons might therefore be used to modify gut motility.

Indexed as

LightAnimalsCalbindin 2ChannelrhodopsinsColonEnteric Nervous SystemGastrointestinal TransitMiceMice, TransgenicModels, AnimalNeuronsOptogeneticsCalb2 protein, mouseCalbindin 2ChannelrhodopsinsColonic Migrating Motor ComplexGut MotilityMyoelectric ComplexPeristalsis

Identifiers

PMID29782847
PMCPMC6715392
OpenAlexW2803823517

What OpenQuestion holds

Textmetadata
LicenceTDM
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.