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  • 1
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Memory - Physiological aspects. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (456 pages)
    Edition: 1st ed.
    ISBN: 9780080932330
    Series Statement: Issn Series
    DDC: 612.823312
    Language: English
    Note: Front Cover -- Copyright page -- Essence of Memory -- List of contributors -- Preface -- Contents -- Section I. Cellular and Molecular Approaches to the Essence of memory -- Chapter 1. Molecular memory traces -- Introduction -- What types of cellular changes underlie memory formation? -- Molecular memory can be dissociated into temporal phases -- Protein-synthesis/gene-expression-dependent memory -- Conclusions -- Abbreviations -- Acknowledgments -- References -- Chapter 2. PKMzeta, LTP maintenance, and the dynamic molecular biology of memory storage -- The discovery of PKMzeta -- PKMzeta is synthesized from a PKMzeta mRNA -- PKMzeta synthesis is regulated by other protein kinases in LTP induction -- PKMzeta potentiates postsynaptic AMPA receptor responses -- PKMzeta maintains late-LTP -- PKMzeta maintains potentiation after synaptic tagging -- PKMzeta maintains long-term spatial memory storage in the hippocampus -- PKMzeta maintains long-term associative memory storage in the neocortex -- Conclusions -- References -- Chapter 3. Understanding the importance of mRNA transport in memory -- Introduction -- mRNA transport in neurons is a dynamic and active mechanism -- The mechanisms of mRNA transport -- The molecular components of RNA granules -- The relevance of mRNA transport in memory -- Conclusions -- Abbreviations -- References -- Chapter 4. Cap-dependent translation initiation and memory -- Regulation of translation -- Localization of translation in the neuron -- Activity-induced regulation of translation initiation machinery -- Lessons learned from the 4E-BP2 knockout mouse -- Translation regulation and disease -- Future directions -- Acknowledgments -- References -- Chapter 5. Translational control of gene expression: a molecular switch for memory storage -- Overview of translation initiation in eukaryotes. , Pharmacologic evidence that translation regulates long-term synaptic plasticity and memory -- Genetic evidence that translation regulates long--term synaptic plasticity and memory -- GCN2 in the brain regulates selection of balanced diet -- A master switch for the conversion from short-term to long-term synaptic plasticity and memory formation -- Summary -- Acknowledgments -- References -- Chapter 6. Regulation of hippocampus-dependent memory by cyclic AMP-dependent protein kinase -- Introduction -- cAMP-dependent protein kinase (PKA) -- Properties of memory -- The role of the cAMP/PKA system in spatial memory -- The role of the cAMP/PKA system in contextual conditioning -- The cAMP/PKA pathway as a target of cognition-enhancing drugs -- Synaptic tagging -- Downstream substrates for PKA in synaptic plasticity and memory storage -- The role of PKA in shaping the essence of memory -- Acknowledgments -- References -- Chapter 7. Synaptic tagging' and 'cross-tagging' and related associative reinforcement processes of functional plasticity as the cellular basis for memory formation -- LTP and LTD as elementary cellular memory models -- Consolidation of LTP and LTD: requirement for protein synthesis -- Consolidation of LTP/LTD: role for transcription? -- LTP/LTD-induction by glutamate receptors -- Non-glutamatergic, neuromodulatory and ''reinforcing'' transmitters required for late plasticity events -- Phases of LTP and LTD -- Input-specificity of late-LTP/LTD via 'synaptic tagging' and by associative properties -- Identifying molecules mediating synaptic tags and the identity of PRPs within functional compartments -- Late-associative properties of LTP and LTD: restriction of associative properties to neuronal compartments -- Physiological, structural and behavioural reinforcement of early-plasticity events by activation of neuromodulatory inputs. , Structural reinforcement: identifying modulatory brain structures -- Behavioural reinforcement: identification of content and interaction of modulatory brain structures -- Concept of 'cellular memory formation' -- Abbreviations -- Acknowledgements -- References -- Chapter 8. Synaptic plasticity in learning and memory: stress effects in the hippocampus -- Introduction: synaptic plasticity, learning, and memory -- Mechanisms underlying synaptic plasticity in the hippocampus -- Acute stress -- Conclusion -- Abbreviations -- Acknowledgments -- References -- Chapter 9. The role of the GluR-A (GluR1) AMPA receptor subunit in learning and memory -- Introduction -- The hippocampus and spatial memory -- AMPA receptors and hippocampus-dependent spatial memory -- GluR-A knockout mice -- Spatial reference memory is GluR-A-independent -- Spatial working memory is GluR-A-dependent -- Spatial working memory on the T-maze -- Genetic rescue of GluR-A-dependent spatial working memory -- GluR-A and performance on conditional learning tasks -- Non-spatial hippocampus-dependent tasks -- NMDA receptors, LTP and spatial memory -- NMDAR mutants and spatial memory -- Dentate-gyrus-specific NR1 knockout selectively impairs spatial working memory -- Is the spatial working memory impairment in GluR-A-/- mice related to frontal or hippocampal processing deficits? -- Understanding the psychological basis of the impairment in GluR-A-/- mice -- Are GluR-A-/- mice more susceptible to proactive interference? -- Two separable forms of hippocampal-dependent, spatial information processing -- Hippocampal GluR-A and priming in short-term memory -- Conclusions -- References -- Chapter 10. Synaptic remodeling, synaptic growth and the storage of long-term memory in Aplysia -- Introduction -- Functional architecture of the synapse -- Synaptic plasticity and memory storage. , Growth of new sensory neuron synapses and the persistence of long-term sensitization -- Time-lapse imaging reveals LTF is associated with presynaptic activation of silent synapses and growth of new functional synapses -- Remodeling of the presynaptic actin network for learning-related synaptic growth requires activation of Cdc42-mediated signaling pathways -- 5-HT-induced internalization of apCAM: a preliminary and permissive step for initiation of learning-related synaptic growth -- Nuclear translocation of apCAM-associated protein (CAMAP) activates presynaptic gene transcription for induction of LTF -- An overall view -- Conclusions -- Acknowledgments -- References -- Chapter 11. Spine dynamics and synapse remodeling during LTP and memory processes -- Introduction -- Morphological changes associated to synaptic plasticity -- Morphological remodeling of activated spines -- Synaptogenesis associated to plasticity -- Mechanisms of plasticity-induced synaptogenesis -- Spine turnover and synapse formation mechanisms -- Memory and synapse formation mechanisms -- Conclusion -- Acknowledgment -- References -- Section II. Systems Approaches to the Essence of Memory -- Chapter 12. The age of plasticity: developmental regulation of synaptic plasticity in neocortical microcircuits -- Plasticity and circuit excitability -- Plasticity in the visual system -- Experience-dependent plasticity in the absence of competition -- Pre-critical period plasticity within layer 4 -- Developmental changes in synaptic properties within cortical layer 4 -- Critical period plasticity within cortical layer 4 -- Experience-dependent rewiring is regulated by cortical development -- Is homeostatic plasticity still induced during the critical period? -- References -- Chapter 13. Differential mechanisms of transmission and plasticity at mossy fiber synapses. , Anatomy of the granule cell mossy fiber axon -- Basic properties of mossy fiber-inhibitory interneuron transmission -- Two types of AMPA/NMDAR populate mossy fiber-interneuron synapses -- Mossy fiber-inhibitory interneuron plasticity -- mGluR7 functions as a trigger for bidirectional plasticity at the mossy fiber-interneuron synapses -- Implications for the mossy fiber-CA3 circuit -- Acknowledgment -- References -- Chapter 14. Long-term synaptic plasticity in hippocampal feedback inhibitory networks -- Different local circuit inhibitory networks in the hippocampus -- Afferent specific mechanisms of transmission -- Afferent-specific short-term synaptic plasticity -- Long-term plasticity -- Consequences of plasticity in interneurons -- Conclusions -- Abbreviations -- Acknowledgments -- References -- Chapter 15. Persistent neural activity in the prefrontal cortex: a mechanism by which BDNF regulates working memory? -- Introduction: working memory and persistent neuronal firing -- Persistent activity and its regulation -- Possible roles of BDNF in the PFC: from working memory to persistent neural activity -- Conclusions -- Abbreviations -- Acknowledgment -- References -- Section III. Animal Approaches to the Essence of Memory -- Chapter 16. Animal models and behaviour: their importance for the study of memory -- Why use animal models to begin with? -- Which animal models? -- Future challenges for animal models: the case of the Aplysia experimental model -- Conclusion -- Abbreviations -- Acknowledgement -- References -- Chapter 17. New tricks for an old slug: the critical role of postsynaptic mechanisms in learning and memory in Aplysia -- Introduction -- Different phases of memory in Aplysia -- Mechanisms of learning-related synaptic facilitation in Aplysia -- Conclusions -- References -- Chapter 18. Olfactory memory traces in Drosophila -- Introduction. , Olfactory-processing circuit in Drosophila.
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  • 2
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Serotonin has been shown to be a neuromodulator in the Aplysia californica CNS. The diversity of serotonin actions is due to the existence of several different receptor subtypes. In this study we report the cloning of a full-length cDNA, coding for a novel serotonin receptor (5-HTap2). The receptor protein bears the characteristics of G protein-coupled receptors. It shares 68% and 34% of its amino acid sequence identity with the 5-HTlym receptor from Lymnaea stagnalis and the mammalian 5-HT1A receptor, respectively. When transfected in HEK 293 cells, 5-HTap2 was negatively coupled to adenylate cyclase. Ligand binding analysis indicated that the order of potencies of various drugs for the inhibition of [3H]LSD binding was: methiothepin 〉 metergoline 〉 5-CT 〉 PAPP 〉 5-HT 〉 ketanserin 〉 NAN-190 〉 8-OH-DPAT 〉 clozapine. RT-PCR amplification of RNA isolated from different tissues indicated that this receptor is expressed in the CNS and in bag cells. The expression of 5-HTap2 restricted to the CNS suggests an important role for this receptor in the modulation of neuronal functions in Aplysia. Moreover, the high expression of 5-HTap2 in the bag cells, associated with its pharmacological profile, suggests that this receptor may be implicated in modulating the afterdischarge during the egg-laying behavior.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: Peptidylglycine α-amidating enzyme (PAM; EC 1.14.17.3) is responsible for the conversion of peptides with a COOH-terminal glycine into α-amidated peptides, a posttranslational modification often required for biological activity and/or increased stability. Such an activity able to convert the model peptide d-Tyr-Val-Gly into d-Tyr-Val-amide was found to be present in the marine mollusk Aplysia californica. Examination of this amidating activity as well as its immunoreactivity demonstrates that (1) it can be found mainly in the atrial gland, heart, and CNS but is barely detectable in the hepatopancreas and gonads, (2) it requires as essential cofactors copper, molecular oxygen, and ascorbate, and (3) it exists in at least two molecular forms, a soluble and a membrane-bound form. Purification of this activity from the atrial gland was accomplished using Cu2+-chelating Sepharose, gel permeation, and hydroxyapatite chromatography. In addition, using polyclonal antibodies raised against various parts of the rat amidating enzyme, we demonstrate that numerous immunologically recognized regions are conserved in both the soluble and membrane-bound Aplysia californica PAM.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: In the marine mollusk Aplysia californica, serotonin initiates three phases of translational regulation: an initial decrease in translation, followed by a transient increase in protein synthesis, both of which are independent of transcription, followed by a later increase in protein synthesis that is dependent on transcription. These increases in protein synthesis may underlie translation-dependent changes in synaptic plasticity. We have characterized the second messenger pathways that underlie these changes in the pleural ganglia of Aplysia. Activation of protein kinase C was both necessary and sufficient for the initial decrease in translation. Protein kinase C, cyclic AMP-dependent protein kinase, and a tyrosine kinase were all required for the second phase, a transient increase in protein synthesis. The late increase in protein synthesis required both protein kinase A and spaced applications of serotonin. Rapamycin, a specific inhibitor of a downstream translational regulator, blocked the transient increase in protein synthesis (second phase), suggesting that this drug may be useful in determining the specific physiological consequences of this translational regulation. Indeed, we used rapamycin to demonstrate that one type of intermediate form of synaptic plasticity induced by serotonin did not require the rapamycin-sensitive increase in translation.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Journal of neurochemistry 68 (1997), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: Peptide diversity can be regulated in many ways. One of the possible mechanisms of such a regulation may lie in the differential processing of a precursor in a tissue-specific manner or in a modulated processing within a single cell. To address these questions the enzymes responsible for the release of active neuropeptides first need to be well characterized. In this study, we have established the cellular distributions of the recently cloned prohormone convertases aPC2 and aPC1B in Aplysia californica and found the distribution of these enzymes to be mainly neuronal and endocrine. We then investigated in two sets of neurons (bag cell neurons and sensory neurons) the possible regulation of these two prohormone convertases by a neurotransmitter known to modulate behavior in Aplysia. In these neurons, we found that only aPC2 is regulated by serotonin possibly via the cyclic AMP cascade. Finally, a study of the biosynthesis of the bag cell egg-laying hormone precursor after treatment with serotonin suggests that such a treatment may increase its processing.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Journal of neurochemistry 89 (2004), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: We have identified an alternatively spliced form of synaptotagmin I in Aplysia neurons. This isoform, synaptotagmin I C2B-β, is generated by alternative exon usage in the C2B domain leading to nine amino acid changes in the C2B sequence from the previously characterized synaptotagmin I, now designated as synaptotagmin I C2B-α. Quantitative reverse transcriptase-polymerase chain reaction demonstrated that approximately 25% of mRNA encoding synaptotagmin I contained the C2B-β exon in the nervous system. Synaptotagmin I C2B-β showed greater resistance to digestion by chymotrypsin in the absence of calcium than did synaptotagmin I C2B-α, although both isoforms required the same amount of calcium to resist chymotrypsin digestion. The source of these changes in C2B properties was mapped to a single amino acid (threonine 358). We have also cloned SNAP 25 in Aplysia and show that it binds synaptotagmin I C2B-β with a higher affinity than synaptotagmin I C2B-α. These results suggest that this splicing alters biochemical properties of the C2B domain, affecting a number of its important known interactions.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 322 (1986), S. 419-422 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] A single learning event initiates several memory processes with different time courses of retention. While short term memory involves covalent modification of pre-existing proteins, the finding that long-term memory requires the expression, during learing, of additional genes, makes it possible to ...
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 329 (1987), S. 62-65 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Activation of cAMP-dependent protein kinase in Aplysia sensory neurons produces short-term sensitization, and it has been proposed2 that the long-term form of this behavioural modification might be mediated by an altered kinase molecule. The holoenzymes of the kinase, composed of regulatory (R) and ...
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We have identified the processes of mechanoreceptor sensory neurons by intracellular injection of horseradish peroxidase in order to study the structure of synapses which exhibit profound, behaviourally-relevant plasticity. These synapses are located at small, varicose expansions along or at the end of the fine, microtubule-containing neurites, and they are crowded with vesicles some of which are associated with the varicosity membrane at regions of membrane specialization morphologically equivalent to active zones described in other species. These active zones occur between pre- and postsynaptic processes at two varieties of apposition: a conventional flat one, and a more elaborate indented one. At indented appositions, the presynaptic varicosity is invaginated by a thin (less than 0.25 μm diameter) spine of variable length. The active zones of indented synapses have approximately twice the vesicle frequency of flat synapses, suggesting that indented synapses are more effective. Sensory neuron terminals are relatively uniform in their structure, having similar concentrations of vesicles and numbers of active zones, and the majority of the processes postsynaptic to them are less than 0.5 μm in diameter. These regularities, and the presence of two strikingly-different types of synaptic apposition, flat and indented, should facilitate structural comparisons of neurons from naive and behaviourally-modified animals. The possible dynamic interconversion of indented and flat appositions at the synaptic terminals of sensory neurons and its behavioural relevance are discussed.
    Type of Medium: Electronic Resource
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