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TESE (Background information (Bliss & Collingridge, 1993 (The role of…
TESE
Background information
Ribeiro, 2003
1) o bloqueio de síntese protéica durante o sono danifica a aquisição de memórias,25
2) padrões de atividade neuronal relacionados às experiências da vigília reaparecem no hipocampo durante o sono.26
Bliss & Collingridge, 1993
1940s: Hebb1 and Konorski2 proposed a coincidence-detection rule in which the synapse linking two cells is strengthened if the cells are active at the same time
Brief trains of high-frequency stimulation to monosynaptic excitatory pathways in the hippocampus cause an abrupt and sustained increase in the efficiency of synaptic transmission. This effect 4, is called long-term potentiation (LTP). LTP has since been found in all excitatory pathways in the hippocampus, as well as in several other regions in the brain, and there is growing evidence that it underlies at least certain forms of memory5,6.
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Bear
Neurotransmitters
The major neurotransmitters fall into one of three chemical categories: (1) amino acids , (2) amines , and (3) peptides.
Neurotransmitter release is triggered by the arrival of an action potential in the axon terminal. The depolarization of the terminal membrane causes voltage-gated calcium channels in the active zones to open.
The resulting elevation in [Ca 2] i is the signal that causes neurotransmitter to be released from synaptic vesicles by a process called exocytosis.
SLEEP
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EEG Rhythms
Delta rhythms are slow, less than 4 Hz, are often large in amplitude, and are a hallmark of deep sleep.
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Alpha rhythms are about 8–13 Hz, are largest over the occipital cortex, and are associated with quiet, waking states
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Gamma rhythms are relatively fast, ranging from about 30–90 Hz, and signal an activated or attentive cortex.
Spindles , brief 8–14 Hz.
Ripples , brief bouts of 80–200 Hz oscillations.