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  • plasticity  (2)
  • Springer  (2)
  • American Society of Hematology
  • Cell Press
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Neuroscience and behavioral physiology 30 (2000), S. 267-276 
    ISSN: 1573-899X
    Keywords: Learning ; sensitization ; memory stages ; neuron ; plasticity ; synaptic facilitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Experiments on common snails showed that three exposures to sensitizing stimuli (10% quinine applied to the snail's head every 15 min) induced synaptic facilitation in defensive behavior command neurons LPl1 and RPl1, with facilitation of responses to sensory stimuli lasting more than 24 h. Application of single stimuli produced transient synaptic facilitation and was expressed in responses to tactile stimulation of the head for about 1 h and in responses to dilute quinine for 3 h. Serotonin and cAMP imitated stimulus-specific transient synaptic facilitation. These substances facilitated the responses of neurons LPl1 and RPl1 to test stimulation of the head without producing changes in the responses to stimulation of other areas of skin on the animal's body. Calmodulin antagonists and glutamate NMDA receptor antagonists inhibited sensitization-induced synaptic facilitation in command neurons. Expression of transient synaptic facilitation depended on protein synthesis—it was suppressed by anisomycin and cycloheximide. It is suggested that transient synaptic facilitation during the acquisition of sensitization is associated with activation of translation/transcription processes and subsequent synthesis of specific short-lived protein molecules with selectively regulate the synaptic “inputs” of command neurons LPl1 and RPl1 from their specific skin innervation zones on the snail's head.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Neuroscience and behavioral physiology 30 (2000), S. 441-447 
    ISSN: 1573-899X
    Keywords: Neuron ; cyclic AMP ; plasticity ; synaptic facilitation ; sensory stimulation ; nociceptive sensitization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Experiments on snails showed that extracellular application of dibutyryl-cAMP (db-cAMP) or intracellular application of cAMP for 30 min evoked increases in excitability and synaptic facilitation in responses to sensory stimulation of defensive behavior command neurons LP11 and RP11. Extitability increased 45–60 min after the start of addition of db-cAMP or cAMP and remained elevated until the end of the experiment (3–4h). Synaptic facilitation started 50–60 min after the onset of extracellular application of db-cAMP and remained detectable in the responses of neurons to tactile stimulation of the head for 1 h and to application of dilute quinine solution for 2–4 h. Application of db-cAMP produced no changes in responses to tactile stimulation of the foot or mantle ridge. Intracellular injection of cAMP induced facilitation of neuron responses only to weak quinine solutions. The responses of neurons to tactile stimulation of the head, foot, and mantle ridge did not change after injections of cAMP. It is suggested that cAMP is involved in the mechanisms controlling the excitability of neurons LP11 and RP11. In addition, cAMP is selectively involved in the postsynaptic mechanism inducing the transient stage of long-term facilitation of synaptic “inputs”, which mediates excitation evoked by chemical stimuli. This set of effects of cAMP is similar to effects arising during the development of nociceptive sensitization and in response to serotonin.
    Type of Medium: Electronic Resource
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