Pharmacogenetic Modulation of Orexin Neurons Alters Sleep/Wakefulness States in Mice

被引:184
|
作者
Sasaki, Koh [1 ]
Suzuki, Mika [1 ]
Mieda, Michihiro [1 ]
Tsujino, Natsuko [1 ]
Roth, Bryan [2 ]
Sakurai, Takeshi [1 ]
机构
[1] Kanazawa Univ, Dept Mol Neurosci & Integrat Physiol, Fac Med, Kanazawa, Ishikawa, Japan
[2] UNC Chapel Hill Med Sch, Chapel Hill, NC USA
来源
PLOS ONE | 2011年 / 6卷 / 05期
关键词
PROTEIN-COUPLED RECEPTORS; OREXIN/HYPOCRETIN NEURONS; RAT-BRAIN; SLEEP; HYPOCRETIN; HOMEOSTASIS; VECTORS; AROUSAL; ROLES; CYCLE;
D O I
10.1371/journal.pone.0020360
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:8
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