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J Appl Physiol (1985). 2011 Sep;111(3):665-72. doi: 10.1152/japplphysiol.00517.2011. Epub 2011 Jun 30.
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.
脑内 microRNA (miRNA) 水平受睡眠剥夺的影响;然而,任何 miRNA 对睡眠的直接影响迄今尚未描述。我们在此报告,脑室内给予 miRNA-132 模拟物(preMIR-132)可减少非快速眼动睡眠(NREMS)的持续时间,同时增加光照相时快速眼动睡眠(REMS)的持续时间。此外,preMIR-132 减少了 NREMS 期间的脑电图(EEG)慢波活动(SWA),这是睡眠强度的指标。在单独的实验中,单侧皮质上给予 preMIR-132 同侧减少了 NREMS 期间的 EEG SWA,但没有改变总睡眠时间。此外,在脑室或皮质内给予 preMIR-132 后,模拟物诱导的作用具有状态特异性,仅在 NREMS 期间发生。在皮质局部给予模拟物后,在表现出与睡眠相关的 EEG 效应时,皮质 miRNA-132 水平更高。我们还报告说,与大鼠黑暗期相比,在睡眠主导的光照期结束时,皮质自发的 miRNA-132 水平较低。结果表明,miRNAs 在睡眠中发挥调节作用,并为研究睡眠调节提供了新的工具。