Murine Multiple Sleep Latency Test: phenotyping sleep propensity in mice
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Updated: Aug 24, 2026

Noninvasive, High-throughput Determination of Sleep Duration in Rodents
Published on: April 18, 2018
Sigrid C Veasey1, Hsu Yeou-Jey, Peter Thayer
1Center for Sleep & Respiratory Neurobiology, University of Pennsylvania School of Medicine, Philadelphia, PA, USA. veasey@mail.med.upenn.edu
Study Objectives:
Objectives were to (1) establish a measure of sleep propensity for a more comprehensive characterization of sleepiness in murine genetics and interventional studies and (2) to characterize sample sizes necessary for statistical differences in effect.
Design:
Average multiple sleep latency values were compared in mice, varying strain, circadian time, and forced-wakefulness conditions.
Subjects:
Adult male mice of inbred strains were studied.
Interventions:
Mice were implanted with electroencephalographic and electromyographic recording electrodes. Twenty-four-hour periods of stable baseline sleep activity (> 600 minutes) were confirmed prior to baseline sleep-latency testing. Average sleep latencies were obtained across 10- and 20-minute nap opportunities within 4 consecutive 30-minute periods. Forced wakefulness protocols were performed prior to additional sleep-latency tests.
Measurements And Results:
Sleep-latency testing with 20-minute nap opportunities every 30 minutes revealed a shorter sleep latency in the lights-on period (12.4 minutes +/- 0.9 vs 16.5 +/- 1, P < .001), a substantial reduction in sleep latencies in mice subjected to 6-hour forced wakefulness (eg, C57BL/6J baseline: 12.4 +/- 0.9 minutes, and forced wakefulness, 8.5 +/- 0.9 minutes, P < .01), and strain differences in latencies following short-term forced wakefulness (P < .01). Sample sizes for 85% power to detect a 25% reduction in the 20-minute daytime Murine Multiple Sleep Latency Test require fewer than 20 mice per group for commonly used transgenic background strains.
Conclusions:
The Murine Multiple Sleep Latency Test is a robust measure of sleep propensity, and the latency varies with homeostatic and circadian influences. The test requires minimal added time to standard murine sleep recordings, yet yields important additive information.

