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  • 1
    Publication Date: 2011-02-19
    Description: Although formation and stabilization of long-lasting associative memories are thought to require time-dependent coordinated hippocampal-cortical interactions, the underlying mechanisms remain unclear. Here, we present evidence that neurons in the rat cortex must undergo a "tagging process" upon encoding to ensure the progressive hippocampal-driven rewiring of cortical networks that support remote memory storage. This process was AMPA- and N-methyl-D-aspartate receptor-dependent, information-specific, and capable of modulating remote memory persistence by affecting the temporal dynamics of hippocampal-cortical interactions. Post-learning reinforcement of the tagging process via time-limited epigenetic modifications resulted in improved remote memory retrieval. Thus, early tagging of cortical networks is a crucial neurobiological process for remote memory formation whose functional properties fit the requirements imposed by the extended time scale of systems-level memory consolidation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lesburgueres, Edith -- Gobbo, Oliviero L -- Alaux-Cantin, Stephanie -- Hambucken, Anne -- Trifilieff, Pierre -- Bontempi, Bruno -- New York, N.Y. -- Science. 2011 Feb 18;331(6019):924-8. doi: 10.1126/science.1196164.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut des Maladies Neurodegeneratives, CNRS UMR 5293, Universites Bordeaux 1 et 2, Talence, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21330548" target="_blank"〉PubMed〈/a〉
    Keywords: Acetylation ; Animals ; Epigenesis, Genetic ; Excitatory Amino Acid Antagonists/pharmacology ; Food Preferences ; Frontal Lobe/*physiology ; Hippocampus/*physiology ; Histones/metabolism ; Learning ; Male ; *Memory, Long-Term ; Neural Pathways ; Neuronal Plasticity ; Neurons/cytology/*physiology ; Odors ; Rats ; Rats, Sprague-Dawley ; Receptors, AMPA/metabolism ; Receptors, N-Methyl-D-Aspartate/metabolism ; Reinforcement (Psychology) ; Signal Transduction ; Synapses/*physiology ; Synaptic Transmission
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2004-07-03
    Description: The hippocampus is crucial for spatial memory formation, yet it does not store long-lasting memories. By combining functional brain imaging and region-specific neuronal inactivation in mice, we identified prefrontal and anterior cingulate cortices as critical for storage and retrieval of remote spatial memories [correction]. Imaging of activity-dependent genes also revealed an involvement of parietal and retrosplenial cortices during consolidation of remote memory. Long-term memory storage within some of these neocortical regions was accompanied by structural changes including synaptogenesis and laminar reorganization, concomitant with a functional disengagement of the hippocampus and posterior cingulate cortex [correction]. Thus, consolidation of spatial memory requires a time-dependent hippocampal-cortical dialogue, ultimately enabling widespread cortical networks to mediate effortful recall and use of cortically stored remote memories independently.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Maviel, Thibault -- Durkin, Thomas P -- Menzaghi, Frederique -- Bontempi, Bruno -- New York, N.Y. -- Science. 2004 Jul 2;305(5680):96-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratoire de Neurosciences Cognitives, CNRS UMR 5106, Universite de Bordeaux 1, Avenue des Facultes, 33405 Talence, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15232109" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain Mapping ; GAP-43 Protein/metabolism ; Gene Expression Regulation ; Genes, Immediate-Early ; Gyrus Cinguli/*physiology ; Immediate-Early Proteins/metabolism ; Lidocaine/pharmacology ; Male ; Memory/drug effects/*physiology ; Mental Recall ; Mice ; Mice, Inbred C57BL ; Neocortex/*physiology ; Nerve Net/physiology ; Neuronal Plasticity ; Neurons/physiology ; Parietal Lobe/physiology ; Prefrontal Cortex/*physiology ; Synapses/physiology ; Time Factors
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2004-05-08
    Description: Although the molecular, cellular, and systems mechanisms required for initial memory processing have been intensively investigated, those underlying permanent memory storage remain elusive. We present neuroanatomical, pharmacological, and genetic results demonstrating that the anterior cingulate cortex plays a critical role in remote memory for contextual fear conditioning. Imaging of activity-dependent genes shows that the anterior cingulate is activated by remote memory and that this activation is impaired by a null alpha-CaMKII mutation that blocks remote memory. Accordingly, reversible inactivation of this structure in normal mice disrupts remote memory without affecting recent memory.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Frankland, Paul W -- Bontempi, Bruno -- Talton, Lynn E -- Kaczmarek, Leszek -- Silva, Alcino J -- New York, N.Y. -- Science. 2004 May 7;304(5672):881-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Departments of Neurobiology, Psychiatry, Psychology and Brain Research Institute, UCLA, 695 Charles Young Drive South, Los Angeles, CA 90095-1761, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15131309" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Calcium-Calmodulin-Dependent Protein Kinase Type 2 ; Calcium-Calmodulin-Dependent Protein Kinases/genetics/metabolism ; Cerebral Cortex/*physiology ; Conditioning (Psychology) ; Cues ; *Fear ; Gene Expression ; Gene Expression Profiling ; Genes, fos ; Gyrus Cinguli/*physiology ; Hippocampus/physiology ; Memory/drug effects/*physiology ; Mental Recall/physiology ; Mice ; Mice, Inbred C57BL ; Neuronal Plasticity ; Neurons/physiology ; Proto-Oncogene Proteins c-fos/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2009-03-17
    Description: Memories are thought to be encoded by sparsely distributed groups of neurons. However, identifying the precise neurons supporting a given memory (the memory trace) has been a long-standing challenge. We have shown previously that lateral amygdala (LA) neurons with increased cyclic adenosine monophosphate response element-binding protein (CREB) are preferentially activated by fear memory expression, which suggests that they are selectively recruited into the memory trace. We used an inducible diphtheria-toxin strategy to specifically ablate these neurons. Selectively deleting neurons overexpressing CREB (but not a similar portion of random LA neurons) after learning blocked expression of that fear memory. The resulting memory loss was robust and persistent, which suggests that the memory was permanently erased. These results establish a causal link between a specific neuronal subpopulation and memory expression, thereby identifying critical neurons within the memory trace.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Han, Jin-Hee -- Kushner, Steven A -- Yiu, Adelaide P -- Hsiang, Hwa-Lin Liz -- Buch, Thorsten -- Waisman, Ari -- Bontempi, Bruno -- Neve, Rachael L -- Frankland, Paul W -- Josselyn, Sheena A -- New York, N.Y. -- Science. 2009 Mar 13;323(5920):1492-6. doi: 10.1126/science.1164139.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Program in Neurosciences and Mental Health, Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19286560" target="_blank"〉PubMed〈/a〉
    Keywords: Amnesia/*physiopathology ; Amygdala/cytology/*physiology ; Animals ; Apoptosis ; Conditioning (Psychology) ; Cyclic AMP Response Element-Binding Protein/genetics/metabolism ; *Fear ; Memory/*physiology ; Mental Recall/*physiology ; Mice ; Mice, Transgenic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    ISSN: 0163-1047
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Psychology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 28 (1990), S. 205-211 
    ISSN: 1741-0444
    Keywords: Biological signal processing ; Diabetic neuropathy ; Heart rate variability ; Respiration ; Sympathetic and parasympathetic nervous systems
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The paper deals with methods of processing ECG and respiration signals which aim at detecting parameters whose values may be correlated to normal and diabetic subjects with or without cardiovascular autonomic neuropathy (CAN). Beatto-beat R-R duration values of the ECG and discrete series of respiration are obtained from original signals using a recognition algorithm. Power spectrum analysis (autospectra, cross-spectra and coherence via autoregressive modelling) is carried out on segments of about 200 consecutive cardiac cycles. Spectral parameters of the R-R variability signal are obtained as follows: total power, power of low-frequency (LF) and high-frequency (HF) components, power of the signal which is (or is not) coherent with respiration, in absolute or in percentage values. The experimental protocol considers 40 diabetic patients (21 of whom have diabetic neuropathy) and 14 normals in three different conditions: resting, standing and controlled respiration. The developed spectral parameters seem sensitive enough to differentiate between normal and pathological subjects. These parameters may constitute a quantitative means to be edded to the classical diabetic tests for the diagnosis of cardiovascular autonomic neuropathy.
    Type of Medium: Electronic Resource
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  • 7
    Publication Date: 2007-02-12
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 8
    Publication Date: 2006-01-09
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 9
    Publication Date: 2009-03-25
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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