Department of Molecular Neuroscience and Integrative Physiology, Faculty of Medicine, Kanazawa University, Kanazawa, Japan.
PLoS One. 2011;6(5):e20360. doi: 10.1371/journal.pone.0020360. Epub 2011 May 27.
Hypothalamic neurons expressing neuropeptide orexins are critically involved in the control of sleep and wakefulness. Although the activity of orexin neurons is thought to be influenced by various neuronal input as well as humoral factors, the direct consequences of changes in the activity of these neurons in an intact animal are largely unknown. We therefore examined the effects of orexin neuron-specific pharmacogenetic modulation in vivo by a new method called the Designer Receptors Exclusively Activated by Designer Drugs approach (DREADD). Using this system, we successfully activated and suppressed orexin neurons as measured by Fos staining. EEG and EMG recordings suggested that excitation of orexin neurons significantly increased the amount of time spent in wakefulness and decreased both non-rapid eye movement (NREM) and rapid eye movement (REM) sleep times. Inhibition of orexin neurons decreased wakefulness time and increased NREM sleep time. These findings clearly show that changes in the activity of orexin neurons can alter the behavioral state of animals and also validate this novel approach for manipulating neuronal activity in awake, freely-moving animals.
表达神经肽食欲素的下丘脑神经元在睡眠和觉醒的控制中起着关键作用。虽然食欲素神经元的活动被认为受到各种神经元输入以及体液因素的影响,但这些神经元在完整动物中的活动变化的直接后果在很大程度上是未知的。因此,我们通过一种称为 Designer Receptors Exclusively Activated by Designer Drugs approach (DREADD) 的新方法研究了食欲素神经元的特异性药物遗传学调节的影响。使用该系统,我们成功地通过 Fos 染色测量了食欲素神经元的激活和抑制。脑电图和肌电图记录表明,兴奋食欲素神经元显著增加了清醒时间,减少了非快速眼动 (NREM) 和快速眼动 (REM) 睡眠时间。抑制食欲素神经元减少了清醒时间,增加了 NREM 睡眠时间。这些发现清楚地表明,食欲素神经元活性的变化可以改变动物的行为状态,并验证了这种用于在清醒、自由运动的动物中操纵神经元活性的新方法。