Evidence map›Paper›PMID 26108871›Full record

ArticleAmerican journal of physiology. Regulatory, integrative and comparative physiology2015

A high-throughput assay for quantifying appetite and digestive dynamics.

Josua Jordi, Drago Guggiana-Nilo, Edward Soucy, Erin Yue Song, Caroline Lei Wee, Florian Engert

Abstract read
In one paragraph

Article in American journal of physiology. Regulatory, integrative and comparative physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Josua JordiDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts; and josuajordi@fas.harvard.edu.
Drago Guggiana-NiloDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts; and Committee for Higher Degrees in Biophysics, Harvard University, Cambridge, Massachusetts.
Edward SoucyDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts; and.
Erin Yue SongDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts; and.
Caroline Lei WeeDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts; and.
Florian EngertDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts; and.
Harvard University · US

Funding

Neural circuits in zebrafish: form, function and plasticityU01NS090449 · NINDS · HARVARD UNIVERSITY · PI CEPKO, CONSTANCE L, ENGERT, FLORIAN · 2014 to 2016
$5.2M
Watching a vertebrate brain learn and behave in a virtual environmentDP1NS082121 · NINDS · HARVARD UNIVERSITY · PI ENGERT, FLORIAN · 2012 to 2015
$3.4M
Monitoring Neural Activity in Freely Behaving Zebrafish Larvae with BioluminescenR01DA030304 · NIDA · HARVARD UNIVERSITY · PI ENGERT, FLORIAN · 2011 to 2014
$1.3M
Transgenic zebrafish for neurobiologyR24NS086601 · NINDS · HARVARD UNIVERSITY · PI ENGERT, FLORIAN · 2014 to 2017
$1.2M
NCCDPHP CDC HHS DP1 NS082121NIDA NIH HHS 5R01DA030304-02NINDS NIH HHS DP1 NS082121NINDS NIH HHS R24 NS086601NINDS NIH HHS U01 NS090449NINDS NIH HHS U01NS090449-01
6 · The paper itself

Abstract

Food intake and digestion are vital functions, and their dysregulation is fundamental for many human diseases. Current methods do not support their dynamic quantification on large scales in unrestrained vertebrates. Here, we combine an infrared macroscope with fluorescently labeled food to quantify feeding behavior and intestinal nutrient metabolism with high temporal resolution, sensitivity, and throughput in naturally behaving zebrafish larvae. Using this method and rate-based modeling, we demonstrate that zebrafish larvae match nutrient intake to their bodily demand and that larvae adjust their digestion rate, according to the ingested meal size. Such adaptive feedback mechanisms make this model system amenable to identify potential chemical modulators. As proof of concept, we demonstrate that nicotine, l-lysine, ghrelin, and insulin have analogous impact on food intake as in mammals. Consequently, the method presented here will promote large-scale translational research of food intake and digestive function in a naturally behaving vertebrate.

Indexed as

AppetiteDigestionEatingFeeding BehaviorHigh-Throughput Screening AssaysOptical ImagingAdaptation, PhysiologicalAnimalsBiomechanical PhenomenaEquipment DesignFluorescent DyesGhrelinImage Processing, Computer-AssistedInsulinLarvaLysineFluorescent DyesGhrelinInsulinLysineNicotineappetiteDiR' dyehungersatiationsatiety

Identifiers

PMID26108871
PMCPMC4538228
OpenAlexW4255612422

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.