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Consciousness, Memory, Language  pocampus, perirhinal, entorhinal and parahip-
                                       pocampal cortex, etc.). It establishes the tem-
       Consciousness. Selective attention, abstract  poral and spatial context surrounding an ex-
       thinking, the ability to verbalize experiences,  perience and recurrently stores the informa-
       the capacity to plan activities based on ex-  tion back into the spines of cortical dendrites in
       perience, self-awareness and the concept of  the association areas (! p. 322). The recur-
       values are some of the many characteristics of  rence of a portion of the experience then suf-
                                       fices to recall the contents of the memory.
       consciousness. Consciousness enables us to
    Central Nervous System and Senses  activity associated with consciousness and  automatically for less than 1 s. A small fraction
                                        Explicit learning (! A) starts in the sensory
       deal with difficult environmental conditions
       (adaptation). Little is known about the brain
                                       memory, which holds the sensory impression
       controlled attention (LCCS, see below), but we
                                       of the information reaches the primary
       do know that subcortical activation systems
                                       memory (short-term memory), which can re-
                                       tain about 7 units of information (e.g., groups
       such as the reticular formation (! p. 322) and
       corticostriatal systems that inhibit the afferent
                                       of numbers) for a few seconds. In most cases,
       signals to the cortex in the thalamus (! p. 326)
                                       the information is also verbalized. Long-term
                                       storage of information in the secondary
       play an important role.
                                       memory (long-term memory) is achieved by
         Attention. Sensory stimuli arriving in the
       sensory memory are evaluated and compared
       to the contents of the long-term memory
                                       is the place where frequently repeated impres-
       within fractions of a second (! A). In routine
                                       sions are stored (e.g., reading, writing, one’s
                                       own name); these things are never forgotten,
    12  situations such as driving in traffic, these  repetition (consolidation). The tertiary memory
       stimuli are unconsciously processed (auto-
                                       and can be quickly recalled throughout one’s
       mated attention) and do not interfere with  lifetime. Impulses circulating in neuronal tracts
       other reaction sequences such as conversation  are presumed to be the physiological correla-
       with a passenger. Our conscious, selective (con-  tive  for  short-term  (primary)  memory,
       trolled) attention is stimulated by novel or am-  whereas biochemical mechanisms are mainly
       biguous stimuli, the reaction to which (e.g., the  responsible for long-term memory. Learning
       setting of priorities) is controlled by vast parts  leads to long-term genomic changes. In addi-
       of the brain called the limited capacity control  tion, frequently repeated stimulation can lead
       system (LCCS). Since our capacity for selective  to long-term potentiation (LTP) of synaptic con-
       attention is limited, it normally is utilized only  nections that lasts for several hours to several
       in stress situations.           days. The spines of dendrites in the cortex play
         The implicit memory (procedural memory)  an important role in LTP.
       stores skill-related information and informa-  Mechanisms for LTP. Once receptors for AMPA
       tion necessary for associative learning (condi-  (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic
       tioning of conditional reflexes; ! p. 236) and  acid) are activated by the presynaptic release of glu-
                                                          +
       non-associative learning (habituation and  tamate (! p. 55 F), influxing Na depolarizes the
       sensitization of reflex pathways). This type of  postsynaptic membrane. Receptors for NMDA (N-
                                       methyl-D-aspartic acid) are also activated, but the
       unconscious memory involves the basal gan-  Ca channels of the NMDA receptors are blocked by
                                        2+
       glia, cerebellum, motor cortex, amygdaloid  Mg , thereby inhibiting the influx of Ca 2+  until the
                                        2+
       body (emotional reactions) and other struc-  Mg 2+  block is relieved by depolarization. The cyto-
                                                      2+
                                           2+
       tures of the brain.             solic Ca concentration [Ca ] i then rises. If this is re-
         The explicit memory (declarative/knowl-  peated often enough, calmodulin mediates the auto-
       edge memory) stores facts (semantic knowl-  phosphorylation of CaM kinase II (! p. 36), which
                                                      2+
       edge) and experiences (episodic knowledge,  persists even after the [Ca ] i falls back to normal.
                                       CaM kinase II phosphorylates AMPA receptors (in-
       especially when experienced by selective at-  creases their conductivity) and promotes their inser-
       tention) and consciously renders the data.  tion into the postsynaptic membrane, thereby en-
       Storage of information processed in the uni-  hancing synaptic transmission over longer periods of
       and polymodal association fields is the re-  time (LTP).
  336  sponsibility of the temporal lobe system (hip-
       Despopoulos, Color Atlas of Physiology © 2003 Thieme
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