Evidence map›Paper›PMID 26863156›Full record

ArticleJournal of visualized experiments : JoVE2016

Spatiotemporal Mapping of Motility in Ex Vivo Preparations of the Intestines.

Derek M Kendig, Norm R Hurst, John R Grider

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  3. BQ788 reveals glial ETBritish journal of pharmacology · 2023
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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

3 authors at 2 institutions in 1 country.

Derek M KendigDepartment of Physiology and Biophysics, Virginia Commonwealth University; Department of Biology, Loyola University Maryland; dmkendig@loyola.edu.
Norm R HurstDepartment of Physiology and Biophysics, Virginia Commonwealth University.
John R GriderDepartment of Physiology and Biophysics, Virginia Commonwealth University.
Virginia Commonwealth University · USLoyola University Maryland · US

Funding

Virginia Commonwealth University IRADCAK12GM093857 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI DANIEL C BULLARD, John J Ryan · 2010 to 2026
$7.0M
ROLE OF GUT PEPTIDES IN INTESTINAL PERISTALSISR01DK034153 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRIDER, JOHN R · 1987 to 2019
$5.5M
Role of Gut Peptides in Intestinal PeristalsisR56DK034153 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRIDER, JOHN R · 2009 to 2009
$351k
ROLE OF GUT PEPTIDES IN INTESTINAL PERISTALSISR23DK034153 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI GRIDER, JOHN R · 1986 to 1986
–
NIDDK NIH HHS DK34153NIDDK NIH HHS R01 DK034153NIDDK NIH HHS R56 DK034153NIGMS NIH HHS K12 GM093857NIGMS NIH HHS K12GM093857
6 · The paper itself

Abstract

Multiple approaches have been used to record and evaluate gastrointestinal motility including: recording changes in muscle tension, intraluminal pressure, and membrane potential. All of these approaches depend on measurement of activity at one or multiple locations along the gut simultaneously which are then interpreted to provide a sense of overall motility patterns. Recently, the development of video recording and spatiotemporal mapping (STmap) techniques have made it possible to observe and analyze complex patterns in ex vivo whole segments of colon and intestine. Once recorded and digitized, video records can be converted to STmaps in which the luminal diameter is converted to grayscale or color [called diameter maps (Dmaps)]. STmaps can provide data on motility direction (i.e., stationary, peristaltic, antiperistaltic), velocity, duration, frequency and strength of contractile motility patterns. Advantages of this approach include: analysis of interaction or simultaneous development of different motility patterns in different regions of the same segment, visualization of motility pattern changes over time, and analysis of how activity in one region influences activity in another region. Video recordings can be replayed with different timescales and analysis parameters so that separate STmaps and motility patterns can be analyzed in more detail. This protocol specifically details the effects of intraluminal fluid distension and intraluminal stimuli that affect motility generation. The use of luminal receptor agonists and antagonists provides mechanistic information on how specific patterns are initiated and how one pattern can be converted into another pattern. The technique is limited by the ability to only measure motility that causes changes in luminal diameter, without providing data on intraluminal pressure changes or muscle tension, and by the generation of artifacts based upon experimental setup; although, analysis methods can account for these issues. When compared to previous techniques the video recording and STmap approach provides a more comprehensive understanding of gastrointestinal motility.

Indexed as

AnimalsColonGuinea PigsMuscle ContractionMuscle TonusPeristalsisPressureVideo Recording

Identifiers

PMID26863156
PMCPMC4781693
OpenAlexW2255854194

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.