ライフサイエンスコーパス: non-REM sleep

1 ical context for memory consolidation during non-REM sleep.

2 ecreased and the EEG was synchronized, as in non-REM sleep.

3 VT but reduced fR only during quiet wake and non-REM sleep.

4 s, but reduced fR only during quiet wake and non-REM sleep.

5 ased VT but raised fR only in quiet wake and non-REM sleep.

6 se long-range correlations break down during non-REM sleep.

7 requency and produced sighs and arousal from non-REM sleep.

8 o subtherapeutic levels for 3 minutes during non-REM sleep.

9 , and maintain breathing automaticity during non-REM sleep.

10 atory stimulation, sighing, and arousal from non-REM sleep.

11 ared with awake mice but are not elevated in non-REM sleep.

12 (milliampere) was increased stepwise during non-REM sleep.

13 such as synaptic downscaling, that occur in non-REM sleep.

14 e the two main oscillations occurring during non-REM sleep.

15 r airway in subjects with sleep apnea during non-REM sleep.

16 term reduction in CBF associated with stable non-REM sleep.

17 graphy scans during presleep wakefulness and non-REM sleep.

18 ence of brain activity from wakefulness into non-REM sleep.

19 ation, one of the fundamental EEG rhythms of non-REM sleep.

20 the suppression of neuronal activity during non-REM sleep.

21 thousands of downstates and spindles during non-REM sleep.

22 ovement (REM) sleep and at minimal levels in non-REM sleep.

23 wakefulness and is infrequently seen during non-REM sleep.

24 in REM sleep and comparable to that seen in non-REM sleep.

25 , (2) the sleep onset period, and (3) stable non-REM sleep.

26 ales, these long timescales are abrogated in non-REM sleep.

27 REM sleep and reduced discharge rates during non-REM sleep.

28 CYT and CBV were observed during waking and non-REM sleep.

29 duces changes in EEG activity during REM and non-REM sleep.

30 icantly between rapid eye movement (REM) and non-REM sleep.

31 de at the expense of decreases in both light non-REM sleep (-24 minutes per decade; P<.001) and REM s

32 the apnea-hypopnea index in REM (AHIREM) and non-REM sleep (AHINREM), respectively.

33 ely tunes the frequency of slow waves during non-REM sleep and anesthesia, and thus provide the first

34 ation between cortical areas is disrupted in non-REM sleep and anesthesia.

35 nic discharge in waking, reduced activity in non-REM sleep and cessation of activity in REM sleep.

36 ve wakefulness during stages 2 and 3 to 4 of non-REM sleep and during REM sleep.

37 ake-active neurons that are quiescent during non-REM sleep and in the case of neurons expressing the

38 oinhibition reduced breathing equally during non-REM sleep and quiet wake.

39 cle activity that occurs from wakefulness to non-REM sleep and reduces airway collapsibility.

40 king accompanied by movement), quiet waking, non-REM sleep and REM sleep.

41 requency and duration of wakefulness, quiet (non-REM) sleep and active (REM) sleep were determined.

42 nt EEG signatures of non-rapid eye movement (non-REM) sleep and are thought to play an important role

43 low-wave activity in non-rapid eye movement (non-REM) sleep and theta and alpha activity during wakef

44 esia, dissociative anesthesia, pharmacologic non-REM sleep, and neuroleptic anesthesia.

45 st in three states of consciousness: waking, non-REM sleep, and REM sleep.

46 s, wakefulness, rapid eye movement (REM) and non-REM sleep are not mutually exclusive states.

47 Slow waves of non-REM sleep are suggested to play a role in shaping sy

48 and finalistic behaviours, normalisation of non-REM sleep by the end of the night, and, in the four

49 During quiet resting and non-REM sleep, C1 cell stimulation (20 s, 2-20 Hz) incre

50 he literature suggests that disturbed REM or non-REM sleep can contribute to maladaptive stress and t

51 However, PPI was smaller at awakening from non-REM sleep compared to established wakefulness (45.4

52 educed during stable non-rapid eye movement (non-REM) sleep compared with the waking level.

53 Stimulation during non-REM sleep decreased PGO wave frequency.

54 abolism changes from presleep wakefulness to non-REM sleep differ in healthy subjects and depressed p

55 ows an episode of partial arousal from early non-REM sleep during which some areas of the brain appea

56 pindles are a universal feature of mammalian non-REM sleep, during which they are presumed to shape a

57 The changes in non-REM sleep EEG spectra are dissimilar from the spectr

58 All models controlled for OSA events during non-REM sleep, either by statistical adjustment or by st

59 During stable non-REM sleep, EMGgg remained below the wakeful baseline

60 nd an increase in muscle tone during REM and non-REM sleep episodes and in the number of awakenings a

61 Our results suggest that REM and non-REM sleep evolved as a differentiation of a single,

62 were significantly different between REM and non-REM sleep (F(1,278) = 5.92; P =.02).

63 s between the hippocampus and the BLA during non-REM sleep following training.

64 ring wakefulness and non-rapid eye movement (non-REM) sleep following each dose of diazepam (p < 0.00

65 lation of rapid eye movement (REM) sleep and non-REM sleep, how mutual inhibition between specific pa

66 During quiet wake or non-REM sleep, hypercapnia (3 or 6% FI,CO2 ) increased b

67 During quiet wake or non-REM sleep, hypercapnia increased both breathing freq

68 .6 +/- 6.2 [SEM]) were studied during stable non-REM sleep in a rigid head-out shell equipped with a

69 atory mechanisms remain active during stable non-REM sleep in children.

70 ormal patterns of cerebral metabolism during non-REM sleep in depressed patients confirmed earlier wa

71 metabolism between presleep wakefulness and non-REM sleep in each group as well as interactions acro

72 the frequency of slow waves recorded during non-REM sleep in freely moving, naturally sleeping-wakin

73 lunteers; (iii) an increase in the length of non-REM sleep in healthy volunteers [49.3 (26.6) versus

74 e, it also reduced EEG spectral power during non-REM sleep in portions of the delta, theta, and alpha

75 ) required to prevent flow limitation during non-REM sleep in subjects with sleep apnea.

76 cose metabolism from presleep wakefulness to non-REM sleep in the left and right laterodorsal frontal

77 o stable entrainment of spindle power during non-REM sleep, nor of theta power during resting wakeful

78 atency to enter rapid eye movement (REM) and non-REM sleep (NREM) than WT.

79 olidated episodes of non-rapid eye movement (non-REM) sleep of minimal common length.

80 rgic neurons in the hypothalamus, which gate non-REM sleep onset.

81 re (undifferentiated non-rapid-eye-movement [non-REM] sleep or poorly structured stage N2, simple mov

82 earing altered daily amounts of wakefulness, non-REM sleep, or REM sleep.

83 ic EMG activity fell in REM as compared with non-REM sleep (p < 0.001).

84 pression with 12 normal men during the first non-REM sleep period at normal bedtime.

85 would be elevated during the first nocturnal non-REM sleep period in depressed patients compared with

86 re, may not be continuously available during non-REM sleep, permitting the cortex to control thalamic

87 erator is in autorhythmic mode (anaesthesia, non-REM sleep, quiet wake).

88 the functional neuroanatomical correlates of non-REM sleep relative to presleep wakefulness in depres

89 Compared with quiet rest and non-REM sleep, REM enhanced the formation of associative

90 tudy shows that compared with quiet rest and non-REM sleep, REM enhances the integration of unassocia

91 was related to EEG oscillatory parameters of non-REM sleep serving as markers of sleep-dependent memo

92 fected with behaviorally abnormal attacks of non-REM sleep ("sleep attacks") and show similar degrees

93 nificantly lower in children with SDB during non-REM sleep (stage 2: P = 0.03; slow-wave sleep: P = 0

94 correlated with rapid eye movement (REM) and non-REM sleep states.

95 PPI of the startle reflex at awakening from non-REM sleep supports the hypothesis that wakefulness i

96 of genioglossus activity from wakefulness to non-REM sleep that occurred on the placebo night.

97 During non-REM sleep the EEG is dominated by slow waves which r

98 While normal regulation of wake/non-REM sleep transitions depends critically upon OX2R a

99 In non-REM sleep, variation in EEG activity between 0.25 an

100 ifically, the transition from wakefulness to non-REM sleep was characterized by the relative persiste

101 low dose, but following 5 mg/kg of diazepam non-REM sleep was increased (p = 0.03) and REM sleep was

102 SDB severity during REM and non-REM sleep was quantified using the apnea-hypopnea in

103 Whole-brain absolute metabolic rate during non-REM sleep was significantly elevated (+47%) in patie

104 a), a period of rapid eye movement (REM) and non-REM sleep, was absent in all animals in which 5-HT d

105 ion can occur in REM sleep and progress into non-REM sleep, with continuous desaturation and hypercar

106 nt a significantly reduced amount of time in non-REM sleep, with postdeprivation recovery sleep hours

107 Spindles and SWRs were initiated during non-REM sleep, yet the changes were incorporated in the