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Calcium/Calmodulin Kinase II in the Pedunculopontine Tegmental Nucleus Modulates the Initiation and Maintenance of Wakefulness
被引:26
作者:
Datta, Subimal
[1
,2
,3
]
O'Malley, Matthew W.
[1
,2
]
Patterson, Elissa H.
[1
,2
]
机构:
[1] Boston Univ, Sch Med, Lab Sleep & Cognit Neurosci, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Dept Psychiat, Boston, MA 02118 USA
[3] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02118 USA
基金:
美国国家卫生研究院;
关键词:
EYE-MOVEMENT SLEEP;
FREELY MOVING RAT;
PONTINE-WAVE GENERATOR;
D-ASPARTATE RECEPTOR;
SIGNAL-REGULATED PROTEIN;
ELEMENT-BINDING PROTEIN;
ACTIVE-AVOIDANCE MEMORY;
SPONTANEOUS REM-SLEEP;
BRAIN-STEM;
CHOLINE-ACETYLTRANSFERASE;
D O I:
10.1523/JNEUROSCI.3981-11.2011
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
The pedunculopontine tegmentum nucleus (PPT) is critically involved in the regulation of wakefulness (W) and rapid eye movement (REM) sleep, but our understanding of the mechanisms of this regulation remains incomplete. The present study was designed to determine the role of PPT intracellular calcium/calmodulin kinase (CaMKII) signaling in the regulation of W and sleep. To achieve this aim, three different concentrations (0.5, 1.0, and 2.0 nmol) of the CaMKII activation inhibitor, KN-93, were microinjected bilaterally (100 nl/site) into the PPT of freely moving rats, and the effects on W, slow-wave sleep (SWS), REM sleep, and levels of phosphorylated CaMKII (pCaMKII) expression in the PPT were quantified. These effects, which were concentration-dependent and affected wake-sleep variables for 3 h, resulted in decreased W, due to reductions in the number and duration of W episodes; increased SWS and REM sleep, due to increases in episode duration; and decreased levels of pCaMKII expression in the PPT. Regression analyses revealed that PPT levels of pCaMKII were positively related with the total percentage of time spent in W(R(2) = 0.864; n = 28 rats; p < 0.001) and negatively related with the total percentage of time spent in sleep(R(2) = 0.863; p < 0.001). These data provide the first direct evidence that activation of intracellular CaMKII signaling in thePPTpromotesWand suppresses sleep. These findings are relevant for designing a drug that could treat excessive sleepiness by promoting alertness.
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页码:17007 / 17016
页数:10
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