Exam 2 (Pt. 9) Flashcards

1
Q

Free-Running Rhythms of Three Animals of Different Species - Onset/Offset

A

The time of activity onset (and offset) occurred earlier (A, B) or later (C) each day. Thus each individual had a free-running period either shorter (A, B) or longer (C) than 24.0 hours.

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2
Q

The Circadian System Model

A
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4
Q

Suprachiasmatic Nucleus (SNC) & Circadian Rhythms

A

Double-plotted drinking record from a squirrel monkey before (A) and after (B, C) receiving a histologically verified total SCN lesion. The approximately 25-h drinking rhythm prelesion (A) persisted with a reduced amplitude for over 90 days postlesion (B) before finally decaying into arrhythmia (C).

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5
Q

Projections of the SCN/Subparaventricular Zone Complex and Their Likely Functions

A
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6
Q

Continuum of States of Arousal

A
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8
Q

Suprachiasmatic Nucleus (SNC) & Circadian Rhythms - Relationship

A

Suprachiasmatic Nucleus (SCN) ablation results in loss of circadian rhythms.

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10
Q

The Arousal Continuum from Highest to Lowest Levels

A
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11
Q

Electrophysiological Correlates of Waking and Sleep Stages - Vertex Spike

A

Characteristic EEG patterns seen during different stages of sleep in humans are shown here. The sharp wave called a vertex spike appears during stage 1 sleep. Brief periods of sleep spindles are characteristic of stage 2 sleep

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12
Q

Electrophysiological Correlates of Waking and Sleep Stages - Deeper Sleep

A

Deeper stages of slow-wave sleep show progressively more large, slow delta waves.

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13
Q

Electrophysiological Correlates of Waking and Sleep Stages - Similarity

A

Note the similarity of activity during waking, stage 1 sleep, and rapid eye movement (REM) sleep.

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14
Q

Properties of Slow-Wave and REM Sleep

A
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15
Q

Sleep Stages & Sleep Architecture

A

Note the progressive lengthening of REM episodes (blue) and the loss of stages 3 and 4 sleep as the night goes on.

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16
Q

Evidence for Bremer’s 1937 Passive Sensory Theory of Sleep - Procedure

A

Transecting the neuraxis at the level between the superior and inferior colliculi removed much of the ascending sensory input to the forebrain.

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17
Q

Evidence for Bremer’s 1937 Passive Sensory Theory of Sleep - Conclusion

A

This produced a cat that appeared to be sleeping; hence, Bremer concluded that depriving the rostral brain produced sleep.

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18
Q

Evidence for Moruzzi and Magoun’s Active Reticular Activating-System Theory of Sleep - Procedure

A

In the late 1940’s Moruzzi and Magoun made small lesions in the core of the brain stem so that most of the classic ascending sensory pathways were left intact.

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19
Q

Evidence for Moruzzi and Magoun’s Active Reticular Activating-System Theory of Sleep - Conclusion

A

Nevertheless, these animals displayed a sleep-like EEG pattern. Hence they concluded that the reticular formation produced sleep through an active process.

20
Q

The Nature & Extent of the Reticular Formation - Diagram

A

MBRF=midbrain reticular formation; MRF=medullary reticular formation; PRF=pontine reticular formation; TRF=thalamic reticular formation; HYP=hypothalamus.

22
Q

Brain Stem Reticular Formation

A

The reticular formation is thought to activate the rest of the brain.

23
Q

Ascending Arousal Systems - Projections

A

The ascending arousal system sends projections from the brainstem and posterior hypothalamus throughout the forebrain.

24
Q

Ascending Arousal Systems - Cholinergic Fibers

A

Neurons of the laterodorsal tegmental nuclei and pedunculopontine tegmental nuclei (LDT and PPT) (blue circles) send cholinergic fibers (ACh) to many forebrain targets, including the thalamus, which then regulate cortical activity.

25
Q

Ascending Arousal Systems - Aminergic Nuclei

A

Aminergic nuclei (green circles) diffusely project throughout much of the forebrain, regulating the activity of cortical and hypothalamic targets directly.

26
Q

Ascending Arousal Systems - Neurotransmitter

A

Neurons of the tuberomammillary nucleus (TMN) contain histamine (HIST), neurons of the raphé nuclei contain 5-HT and neurons of the locus coeruleus (LC) contain noradrenaline (NA).

27
Q

Ascending Arousal Systems - Sleep-Promoting

A

Sleep-promoting neurons of the ventrolateral preoptic nucleus (VLPO, red circle) contain GABA and galanin (Gal).

28
Q

Descending Projections from the Ventrolateral Preoptic Area (VLPO) that Terminate on Major Brain Stem “Arousal Nuclei” - VLPO Axon

A

Axons from the VLPO directly innervate the cell bodies and proximal dendrites of neurons in the major monoamine arousal groups.

29
Q

Descending Projections from the Ventrolateral Preoptic Area (VLPO) that Terminate on Major Brain Stem “Arousal Nuclei” - Interneuron

A

Within the major cholinergic groups, axons from the VLPO mainly innervate interneurons, rather than the principal cholinergic cells.

30
Q

Hypocretin/Orexin Arousal Mechanisms - Effects On

A
31
Q

Hypocretin/Orexin Arousal Mechanisms - Orexin-Stimulating

A
32
Q

Hypocretin/Orexin Arousal Mechanisms - Hypocretin Arousal Pathway

A
33
Q

The Neural Substrates for the Interaction of Circadian Rhythm Control and Arousal/Sleep Mechanisms

A
34
Q

A Model of Sleep Employing the Concept of an Interaction Between a Circadian Rhythmic Process and a Sleep-Wake Process - Main Idea

A

Sleep is assumed to result from the action of process C and process S.

35
Q

A Model of Sleep Employing the Concept of an Interaction Between a Circadian Rhythmic Process and a Sleep-Wake Process - Rhythmicity

A

Process C follows a circadian rhythm and is independent of sleeping and waking.

Rhythmicity Process S, on the other hand, depends on sleep-wake behavior; S declines during sleep and rises continuously during sleep deprivation.

37
Q

Variation in States of Arousal - Variation

A

Over the course of time, physiological, behavioral and cognitive functions vary in level of arousal/intensity.

38
Q

Variation in States of Arousal - Reason

A

The fluctuations depend upon changes in neural activity at both the systems and cellular levels.

39
Q

Variation in States of Arousal - Level

A

At a system level, there are neural substrates that control rhythmic changes in level of arousal.

At a cellular level, neurotransmitters and drugs affecting these neurotransmitters act to change levels of activity and arousal.

51
Q

The Nature & Extent of the Reticular Formation - Conclusion

A

The concept of a reticular activating system has changed dramatically from the time of Moruzzi and Magoun’s experiments. Specific cell groups containing NE, ACh and 5HT have been implicated in projections to the thalamus and cortex and as being important in the control of arousal.