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Published on: August 2, 2017
MicroRNA 132 alters sleep and varies with time in brain
Christopher J Davis1, James M Clinton, Ping Taishi
1Washington State University-Spokane, Health Sciences Bldg. 280E, 412 E Spokane Falls Blvd., Spokane, WA 99202, USA. cjdavis@wsu.edu
Abstract:
MicroRNA (miRNA) levels in brain are altered by sleep deprivation; however, the direct effects of any miRNA on sleep have not heretofore been described. We report herein that intracerebroventricular application of a miRNA-132 mimetic (preMIR-132) decreased duration of non-rapid-eye-movement sleep (NREMS) while simultaneously increasing duration of rapid eye movement sleep (REMS) during the light phase. Further, preMIR-132 decreased electroencephalographic (EEG) slow-wave activity (SWA) during NREMS, an index of sleep intensity. In separate experiments unilateral supracortical application of preMIR-132 ipsilaterally decreased EEG SWA during NREMS but did not alter global sleep duration. In addition, after ventricular or supracortical injections of preMIR-132, the mimetic-induced effects were state specific, occurring only during NREMS. After local supracortical injections of the mimetic, cortical miRNA-132 levels were higher at the time sleep-related EEG effects were manifest. We also report that spontaneous cortical levels of miRNA-132 were lower at the end of the sleep-dominant light period compared with at the end of the dark period in rats. Results suggest that miRNAs play a regulatory role in sleep and provide a new tool for investigating sleep regulation.
Insights
MicroRNA-132 (miRNA-132) directly impacts sleep architecture. Enhancing miRNA-132 levels reduced non-rapid-eye-movement sleep (NREMS) and slow-wave activity (SWA), suggesting a regulatory role in sleep.
Area of Science:
- Neuroscience
- Molecular Biology
- Sleep Science
Background:
- Brain microRNA (miRNA) levels are affected by sleep deprivation.
- The specific role of individual miRNAs in regulating sleep remains largely undescribed.
Purpose of the Study:
- To investigate the direct effect of microRNA-132 (miRNA-132) on sleep regulation.
- To explore the impact of miRNA-132 manipulation on sleep architecture and intensity.
Main Methods:
- Intracerebroventricular and unilateral supracortical administration of a miRNA-132 mimetic (preMIR-132) in rats.
- Electrophysiological recordings (EEG) to measure sleep parameters, including non-rapid-eye-movement sleep (NREMS), rapid eye movement sleep (REMS), and slow-wave activity (SWA).
- Measurement of cortical miRNA-132 levels following mimetic injection.
Main Results:
- Intracerebroventricular preMIR-132 decreased NREMS duration and increased REMS duration during the light phase.
- PreMIR-132 administration reduced EEG slow-wave activity (SWA) during NREMS, indicating decreased sleep intensity.
- Effects were state-specific to NREMS and localized to the injection site after supracortical application.
- Cortical miRNA-132 levels increased post-injection, correlating with observed EEG effects.
- Spontaneous cortical miRNA-132 levels were lower at the end of the light period compared to the dark period.
Conclusions:
- MicroRNAs, specifically miRNA-132, play a direct regulatory role in modulating sleep.
- miRNA-132 influences both sleep duration and intensity (SWA).
- These findings offer a novel tool for studying sleep regulation mechanisms.
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