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Updated: Dec 20, 2025

High-throughput Measurement of Gut Transit Time Using Larval Zebrafish
Published on: October 23, 2018
An automated sensitive approach for measuring whole gut transit time
Keeley L Baker1,2, Michelle Izydorczak1, Ruaidhri Jackson3
1The John B. Pierce Laboratory, New Haven, CT, USA.
Background:
Commonly used methods to measure whole gut transit time in rodents have yet to combine high sensitivity, objectivity, and automation. We have developed a novel method using oral gavage of non-toxic fluorescent dye particles and their detection by fluorescence imaging to enable unbiased automated detection of gut transit time simultaneously in 8 cages.
Methods:
Naïve mice (n = 20) were gavaged with a non-caloric viscous suspension of 4.4% fluorescent dye in 3 groups on 2 occasions. Each group was imaged in 8 cages at 5-minute intervals using blue LEDs for illumination and a Sony full-frame mirrorless camera with a green band-pass emission filter. Custom MATLAB code counted the number of fluorescent boli per cage post hoc and provided graphical and spreadsheet output. Boli counts across a wide range of parameters were compared to blind assessments by an experimenter.
Results:
Fluorescent boli were detected with high sensitivity, while unstained boli were readily rejected. All cages showed no fluorescent boli for the first ~20 frames (100 minutes), after which many cages gradually show a rise to 1-6 fluorescent boli. The mean time to first fluorescent bolus in each session was 264 ± 141 and 223 ± 81 minutes post-gavage, with no within subject consistency. There was high correlation between automated scores and that of experimenter (r = .95 ± .02), being robust to parameter changes.
Conclusions And Inferences:
This novel approach provides a reliable, automatic, and low-cost method of measuring gastrointestinal transit time in mice.
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