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sleep
(Review)
Sergey Skudaev
Introduction
It is known that sleep is very important for health and essential for surviving. Sleep
deprivation leads to death within three weeks. However the purpose of sleep still is not
clearly understood. Two fundamental processes carry out regulation of sleep: circadian
rhythm and homeostasis.
Circadian rhythm determines temporal organization of daily activity of the hormonal and
nervous system. For example, rats are awake at night and sleep during the day.
At the beginning of 20th century, scientists believed that sleep is a rest state of our brain
and body. In 1950s it was discovered that brain activity, brain blood flow; blood pressure
and heart rate in some sleep stages might be the same as in wakefulness.
It has been shown that sleep is essential for adaptation to stress and to learning.
Consolidation of short-term memory in long term takes place in sleep. In sleep our brain
is planning our future actions and is testing their outcomes.
A normal EEG of relaxed person who closed his/her eyes usually displays well-
synchronized waves with frequency around 10 per second and amplitude about 50 micro
volts. These waves are called alpha waves or alpha rhythms. A light or sound stimuli
cause desynchronization of EEG; alpha waves are replaced with low voltage and high
frequency beta waves. Beta waves may appear without external stimuli, when person
performs a calculation or is involved in some other activity. Grey Walter [] 1952.
During sleep EEG waves are changing from high frequency and low voltage to low
frequency and high voltage (synchronization of neuronal activity). About every 70-80
minutes of sleep the EEG becomes similar to that in wake state; blood flow through the
brain increases, tonus of skeletal muscles dramatically drops, and rapid eye movement
(REM) is observed. This state of sleep is called REM sleep. Persons who wake up in
REM sleep describe vivid colorful visual dreams. REM sleep is also called Fast-Waves
Sleep, while Non-REM sleep is called Slow Waves Sleep.
Two graduate students: Eugene Aserinsky and Nathaniel Kleitman from the laboratory of
William C. Dement [] at the University of Chicago discovered and described REM sleep
in the early 50s. At birth, REM sleep composes 90% of the total amount of sleep.
Sleep in adult human comprises of 90 minutes cycles of Non-REM and REM sleep. REM
sleep constitutes about 20% of total sleep time. First REM sleep episode lasts about 5-10
minutes. The length of the REM sleep phase increases toward the morning.
Deprivation of REM sleep during one night leads to increasing the total REM sleep the
next night. Long deprivation of REM sleep may cause hallucination and psychotic
disorders.
The muscle atonia in REM sleep increases resistance of the upper airway and as a result
obstructive sleep apnea (OSA) may occur in some individuals. OSA is characterized by
the frequent temporary interruption of breathing during sleep. Inhibition of hypoglossal
motoneurons, which control tongue movement, may contribute to OSA during REM
sleep. Bellingham M. C, Funk G.D [] (2000). It is believed that Sudden Infant Death
Syndrome (SIDS) also occurs in REM sleep.
Deprivation of REM sleeps in rats for as long as 20 days causes loss of weight in spite of
increased food consumption. M. Koban and K. L. Swinson [] 2005. REM sleep
deprivation in rats usually is achieved with a very simple method. A flowerpot is placed
upside down in bath with water. A rat is sitting on the top of the flowerpot. In REM sleep
stage rat muscles are loosing tonus and as a result, the rat falls in the water and wakes up.
Then it climbs back on the top of the flowerpot and may sleep in Non-REM stage until it
falls in the water in the next REM stage. REM sleep deprived rat metabolism rose to
166% of baseline.
Non-REM sleep consists of four stages. A. Rechtschaffen, J. Siegel [] 2000. The first
stage of sleep is characterized by transition from wakefulness to sleep. It lasts few
minutes. EEG of the first stage shows low-amplitude mix frequency waves.
EEG in the second stage shows periods of well-synchronized sinusoidal waves 12-14 per
second. These groups of waves are spindle shape and are called sleep spindles.
In the third sleep stage slow, high-amplitude waves appear in the EEG every 0.5-2
seconds.
Global decrease of cerebral blood flow (CBF), oxygen and glucose metabolism are
observed in slow wave sleep (SWS). No difference in CBF, oxygen and glucose
metabolism were observed between REM sleep and wakefulness. Regional cerebral
blood flow (rCBF ) was significantly decreased in the pons, midbrain, thalamus and basal
forebrain during SWS. There was no significant decrease of CBF in primary or secondary
sensory cortex, which implies that sensory systems remain functional during the sleep.
Kajimura N. et al. 1999. Hofle N et al. 1997.
Later it was discovered that stimulation of the posterior hypothalamus produces EEG
activation, while stimulation of the anterior hypothalamus promotes sleep. The pons,
midbrain tegmentum, and the thalamus comprise the ascending reticular activating
system. Steriade and McCarley 1990.
It is believed that the thalamic inhibitory mechanism is responsible for transition from
wakefulness to sleep. The sleep spindles are generated in the thalamus from onset of
sleep. It is thought that spindle waves block activating input from the stem reticular
system to the cerebral cortex at the thalamic level and as a result initiate and maintain
sleep. B.M.Evans [] 2002.
The medullar reticular system also inhibits the midbrain activating reticular formation
promoting sleep. Moruzzi, Magoun [] 1949.
Neurochemistry of sleep
Neural cell and synapses
Neural cell or neuron has many dendrites, which look like trees and serve for receiving
information. One long processor - axon serves for output information. The body of neural
cell and its dendrites are covered with thousand of synapses.
Through these synapses, the dendrites receive messages from the other neurons. These
messages can inhibit or increase neuron activity. In the latter case, neuron may generate
action potential, which spreads along the axon.
The synapse contains vesicles with neurotransmitter. When action potential reaches axon
terminal, its membrane becomes permeable to Ca++ ions. Ca++ ions flow inside the
terminal and cause vesicles to move to presynaptic membrane and release transmitter in
synaptic cleft. The transmitter molecules passively spread in the synaptic cleft and reach
postsynaptic membrane receptors. Transmitter binds to receptors and change potential of
postsynaptic membrane. Message is transferred to the next neuron.
It is located in the dorsolateral pons. In 1960s it was discovered that the locus coeruleus
is the major source of norepinephrine (noradrenalin) in the brain. Its neurons produce
norepinephrine and send projections to spinal cord, brainstem, midbrain, cerebellum,
hippocampus, thalamus, and cerebral cortex.
The locus coeruleus (LC) receive projections from many different brain regions, which
release such wide specter of neurotransmitters as opiates, glutamate, GABA, serotonin,
epinephrine. Aston-Jones G et al. 1991.
Hypocretin (Orexin)
The hypocretins are thought to play a primary role in the control of sleep and
wakefulness as well as attention, learning, memory, feeding-energy regulation and
modulation of pain at all levels of spinal cord. Ebrahim I.O. et al. []2002
The dorsal raphe nucleus (DRN) contains the largest pool of serotonergic neurons in the
brain. The raphe sends predominantly inhibitory serotonergic projections to the dentate
gyrus and moderate projections to Ammon's horn regions of the hippocampus. These
projections end on the hippocampal interneurons. Microinjections of the 5-HT1a receptor
agonist 8-hydroxy-2-(di-n-propylamino)-tetralin (8-OH-DPAT) in median raphe increases
anxiety. This compound inhibits serotonergic neurons in the median and dorsal raphe.
The microinjection of the 8-OH-DPAT in median raphe increases the hippocampal theta
rhythm amplitude and the movement velocity of the freely behaving rats. Nitz D.A.,
McNaughton B.L. 1999. The dorsal raphe sent major projections to the dorsolateral pons
which promotes REM sleep. The microinjections of the 8-OH-DPAT in the dorsal raphe
increases REM sleep.
The limbic cortical and diencephalic structures control the activity of the median and
dorsal raphe serotonergic neurons by modulation of GABAergic neurons in the raphe
nuclei. Varga et al. 2001, 2003. The activity of serotonergic neurons of the dorsal raphe
nuclei decreases from waking through slow wave sleep to REM sleep, while the activity
of the GABAergic neurons increases. The GABAergic neurons in the raphe nuclei may
decrease the ascending serotonergic output by direct inhibition of serotonergic neurons or
increase it by inhibition of GABA interneurons.
The serotonergic ascending pathway inhibits hippocampal theta rhythm and causes
desynchronization of EEG. The GABA interneurons also inhibit glutamatergic
projections from median raphe to the limbic theta rhythm generators. The blockade of the
GABA receptors activates glutamatergic pathway and promote theta rhythm. Li et al.
2005.
Lesions in centralis superior raphe (CeSR) and reticularis pontis nuclei (RPN) in cats
decrease slow wave sleep (SWS) and parodoxal sleep (PS) and increase wakefulness.
Drowsiness was increase during the light "day time" phase but not during the dark phase.
Recent study indicated that histaminergic neurons also play an important role in memory
and learning by direct influence on memory or by modulating release of acetylcholine.
(AC). Blandina P. et al 2004. Histominergic neurons are located in the tuberomammillary
nucleus (TMN) of the hypothalamus. TMN send projections to different brain areas and
modulates activity of cholinergic neurons. Histaminergic neurons promote wakefulness
and emotional memory. Their activity is high during wakefulness and attention and low
during sleep.
It is known that the baselateral amygdala (BLA) activity related to emotional memory.
Histominergic neurons regulate acetylcholine release in amygdala. Microinjections of
histamine in BLA impaired learning in animals conditioned to escape from the
punishment box. In the neocortex, microinjections of histamine decreases cholinergic
tone through H3 receptors. The systemic administration of H3 receptor agonists impairs
rat performance in learned tasks.
The recent study shows that nitric oxide synapses exist on the cholinergic neurons of the
laterodorsal and pedunculopontine tegmental nuclei, which send projections to the medial
pontine reticular formation (mPRF). Stimulation of mPRF evokes REM sleep-like state
and causes hypotonia of the upper airway muscles. mPRF microinjection of Ng-nitro-L-
arginine (NLA), which inhibits nitric oxide synapses in mPRF, significantly decrease the
duration of REM sleep. It is thought that nitric oxide increases the release of AC in mPRF
and promotes REM sleep. Leonard T.O. et al.1997.
Dopamine
The substantia nigra is the major source of dopamine in the brain. Noradrenergic and
serotonergic neurons become silent during REM sleep whereas dopaminergic neurons
remain active which produce "psychotic-like mental activity of dreaming" Gottesmann C.
(2002)
Reduction in the number of dopaminergic neurons in the substantia nigra causes REM
sleep behavior disorder (RBD), which is characterized by a loss of skeletal muscle atonia
during REM sleep. Patients with RBD have aggressive dreams in which they can injure
their bed partners. The dopamine neuron loss increases activity of the globus pallidum,
which inhibits midbrain structures. These structures inhibit the spinal motoneurons and
their inhibition prevents development of skeletal muscle atonia during REM sleep.
Eisensehr et al 2000.
Neuropeptid S
One more group of neurons was discovered recently between locus coeruleus and
Barrington nucleus. These neurons release neuropeptid S (NPS) that elevates arousal and
at the same time produce anxiolytic-like effect. NPS receptors were found in neocortex,
thalamus, hypothalamus and amygdale. It is well known that the amygdale participate in
modulation of fear and anxiety. Probably, a unique anxiolytic effect of NPS is related to
modulation of the amygdale activity by NPS. Reinscheid R.K. and Xu Y.2005
How slow-wave sleep with low level of acetylcholine influents memory consolidation? It
is proposed that there are two stage of memory consolidation. In the first stage during the
wakefulness and REM sleep neocortex sends newly acquired information to the
hippocampus, while acetylcholinergic projections release acetylcholine and suppress
hippocampal feedback to neocortex. During slow-wave sleep, when acetylcholine level is
low and hippocampal feedback to the neocortex is released, memory traces temporary
stored in hippocampal circuitry are transmitt back to the neocortex.
It is thought that the release of acetylcholine in the neocortex controls the flow of
information from hippocampus to the neocortex. The improvement of the declarative
tasks performance after slow-wave sleep can be blocked by anticholinesterase drug. In
the same experiments, the performance of procedural tasks was not impaired, which
suggest that procedural memory consolidation may depend more on REM sleep.
It is proposed that REM sleep with high level of acetylcholine enhance synaptic plasticity
and memory consolidation. Guis, S & Born 2004 in Power A.E. 2004.
Conclusion
In spite of the great progress in sleep research, it is still not possible to draw the whole
picture of sleep mechanisms and understand the sleep purpose. Many neuroanatomic
structures with different neurotransmitters at all levels of brain from the brainstem
medulla to the thalamus and cerebral cortex participate in regulation of the sleep-wake
cycle. Probably, understanding sleep is almost the same as understanding the brain.
It does not mean that we cannot treat sleep disorders. The recent progress in
neurochemistry and pharmacology of sleep gives us some hope.
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