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  1. Article ; Online: Automated Detection and Localization of Synaptic Vesicles in Electron Microscopy Images.

    Imbrosci, Barbara / Schmitz, Dietmar / Orlando, Marta

    eNeuro

    2022  Volume 9, Issue 1

    Abstract: Information transfer and integration in the brain occurs at chemical synapses and is mediated by the fusion of synaptic vesicles filled with neurotransmitter. Synaptic vesicle dynamic spatial organization regulates synaptic transmission as well as ... ...

    Abstract Information transfer and integration in the brain occurs at chemical synapses and is mediated by the fusion of synaptic vesicles filled with neurotransmitter. Synaptic vesicle dynamic spatial organization regulates synaptic transmission as well as synaptic plasticity. Because of their small size, synaptic vesicles require electron microscopy (EM) for their imaging, and their analysis is conducted manually. The manual annotation and segmentation of the hundreds to thousands of synaptic vesicles, is highly time consuming and limits the throughput of data collection. To overcome this limitation, we built an algorithm, mainly relying on convolutional neural networks (CNNs), capable of automatically detecting and localizing synaptic vesicles in electron micrographs. The algorithm was trained on murine synapses but we show that it works well on synapses from different species, ranging from zebrafish to human, and from different preparations. As output, we provide the vesicle count and coordinates, the nearest neighbor distance (nnd) and the estimate of the vesicles area. We also provide a graphical user interface (GUI) to guide users through image analysis, result visualization, and manual proof-reading. The application of our algorithm is especially recommended for images produced by transmission EM. Since this type of imaging is used routinely to investigate presynaptic terminals, our solution will likely be of interest for numerous research groups.
    MeSH term(s) Animals ; Humans ; Mice ; Microscopy, Electron ; Presynaptic Terminals ; Synapses ; Synaptic Vesicles ; Zebrafish
    Language English
    Publishing date 2022-01-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2800598-3
    ISSN 2373-2822 ; 2373-2822
    ISSN (online) 2373-2822
    ISSN 2373-2822
    DOI 10.1523/ENEURO.0400-20.2021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Subiculum as a generator of sharp wave-ripples in the rodent hippocampus.

    Imbrosci, Barbara / Nitzan, Noam / McKenzie, Sam / Donoso, José R / Swaminathan, Aarti / Böhm, Claudia / Maier, Nikolaus / Schmitz, Dietmar

    Cell reports

    2021  Volume 35, Issue 3, Page(s) 109021

    Abstract: Sharp wave-ripples (SWRs) represent synchronous discharges of hippocampal neurons and are believed to play a major role in memory consolidation. A large body of evidence suggests that SWRs are exclusively generated in the CA3-CA2 network. In contrast, ... ...

    Abstract Sharp wave-ripples (SWRs) represent synchronous discharges of hippocampal neurons and are believed to play a major role in memory consolidation. A large body of evidence suggests that SWRs are exclusively generated in the CA3-CA2 network. In contrast, here, we provide several lines of evidence showing that the subiculum can function as a secondary SWRs generator. SWRs with subicular origin propagate forward into the entorhinal cortex as well as backward into the hippocampus proper. Our findings suggest that the output structures of the hippocampus are not only passively facilitating the transfer of SWRs to the cortex, but they also can actively contribute to the genesis of SWRs. We hypothesize that SWRs with a subicular origin may be important for the consolidation of information conveyed to the hippocampus via the temporoammonic pathway.
    MeSH term(s) Animals ; Brain Waves/physiology ; CA1 Region, Hippocampal/anatomy & histology ; CA1 Region, Hippocampal/physiology ; CA3 Region, Hippocampal/anatomy & histology ; CA3 Region, Hippocampal/physiology ; Electrodes, Implanted ; Entorhinal Cortex/anatomy & histology ; Entorhinal Cortex/physiology ; Male ; Memory Consolidation/physiology ; Mice ; Mice, Inbred C57BL ; Microtomy ; Neurons/cytology ; Neurons/physiology ; Patch-Clamp Techniques ; Rats ; Rats, Long-Evans ; Synaptic Potentials/physiology ; Synaptic Transmission/physiology
    Language English
    Publishing date 2021-04-18
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2021.109021
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Neue Befunde zur Funktion der GABAergen Hemmung während post-läsionaler Reorganisation im visuellen Kortex

    Imbrosci, Barbara / Mittmann, Thomas

    Neuroforum

    2014  Volume 20, Issue 1, Page(s) 178

    Language German
    Document type Article
    ZDB-ID 1238592-x
    ISSN 0947-0875
    Database Current Contents Medicine

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  4. Article ; Online: Physiological properties of supragranular cortical inhibitory interneurons expressing retrograde persistent firing.

    Imbrosci, Barbara / Neitz, Angela / Mittmann, Thomas

    Neural plasticity

    2015  Volume 2015, Page(s) 608141

    Abstract: Neurons are polarized functional units. The somatodendritic compartment receives and integrates synaptic inputs while the axon relays relevant synaptic information in form of action potentials (APs) across long distance. Despite this well accepted notion, ...

    Abstract Neurons are polarized functional units. The somatodendritic compartment receives and integrates synaptic inputs while the axon relays relevant synaptic information in form of action potentials (APs) across long distance. Despite this well accepted notion, recent research has shown that, under certain circumstances, the axon can also generate APs independent of synaptic inputs at axonal sites distal from the soma. These ectopic APs travel both toward synaptic terminals and antidromically toward the soma. This unusual form of neuronal communication seems to preferentially occur in cortical inhibitory interneurons following a period of intense neuronal activity and might have profound implications for neuronal information processing. Here we show that trains of ectopically generated APs can be induced in a large portion of neocortical layer 2/3 GABAergic interneurons following a somatic depolarization inducing hundreds of APs. Sparsely occurring ectopic spikes were also observed in a large portion of layer 1 interneurons even in absence of prior somatic depolarization. Remarkably, we found that interneurons which produce ectopic APs display specific membrane and morphological properties significantly different from the remaining GABAergic cells and may therefore represent a functionally unique interneuronal subpopulation.
    MeSH term(s) Action Potentials ; Animals ; GABAergic Neurons/cytology ; GABAergic Neurons/physiology ; Interneurons/cytology ; Interneurons/physiology ; Mice, Inbred C57BL ; Neocortex/cytology ; Neocortex/physiology ; Synapses/physiology
    Language English
    Publishing date 2015-02-11
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1454938-4
    ISSN 1687-5443 ; 2090-5904 ; 0792-8483
    ISSN (online) 1687-5443
    ISSN 2090-5904 ; 0792-8483
    DOI 10.1155/2015/608141
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Neuronal mechanisms underlying transhemispheric diaschisis following focal cortical injuries.

    Imbrosci, Barbara / Wang, Yibao / Arckens, Lutgarde / Mittmann, Thomas

    Brain structure & function

    2015  Volume 220, Issue 3, Page(s) 1649–1664

    Abstract: Unilateral cortical lesions cause disturbances often spreading into the hemisphere contralateral to the injury. The functional alteration affecting the contralesional cortex is called transhemispheric diaschisis and is believed to contribute to ... ...

    Abstract Unilateral cortical lesions cause disturbances often spreading into the hemisphere contralateral to the injury. The functional alteration affecting the contralesional cortex is called transhemispheric diaschisis and is believed to contribute to neurological deficits and to processes of functional reorganization post-lesion. Despite the profound implications for recovery, little is known about the cellular mechanisms that underlie this phenomenon. In the present study, transhemispheric diaschisis was investigated with an in vivo-ex vivo model of unilateral lesions, induced by an infrared laser in rat visual cortex. Visually evoked cortical activity was evaluated by the expression level of the cellular activity marker zif268, which showed an elevation in the cortex contralateral to the lesion. In vitro patch-clamp recordings from layer 2/3 pyramidal neurons revealed a shift in the excitatory–inhibitory balance in favor of excitability, particularly expressed in the undamaged hemisphere. Layer 5 principal neurons displayed an increased spontaneous firing rate contralateral to the lesion, while cells of the injured cortex displayed a reduced firing upon somatic current injection. These data suggest that a cortical lesion triggers an enhanced neuronal activity in the hemisphere contralateral to the damage. Our findings constitute an important step toward the understanding of transhemispheric diaschisis on the cellular level.
    MeSH term(s) Animals ; Brain Injuries/physiopathology ; Cerebral Cortex/injuries ; Cerebral Cortex/metabolism ; Cerebral Cortex/pathology ; Cerebral Cortex/physiopathology ; Early Growth Response Protein 1/metabolism ; Excitatory Postsynaptic Potentials ; Functional Laterality/physiology ; Inhibitory Postsynaptic Potentials ; Neurons/metabolism ; Neurons/physiology ; Photic Stimulation ; RNA, Messenger/metabolism ; Rats ; Rats, Long-Evans ; Synapses/physiology ; Visual Cortex/injuries
    Chemical Substances Early Growth Response Protein 1 ; Egr1 protein, rat ; RNA, Messenger
    Language English
    Publishing date 2015
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2273162-3
    ISSN 1863-2661 ; 1863-2653
    ISSN (online) 1863-2661
    ISSN 1863-2653
    DOI 10.1007/s00429-014-0750-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Subiculum as a generator of sharp wave-ripples in the rodent hippocampus

    Barbara Imbrosci / Noam Nitzan / Sam McKenzie / José R. Donoso / Aarti Swaminathan / Claudia Böhm / Nikolaus Maier / Dietmar Schmitz

    Cell Reports, Vol 35, Iss 3, Pp 109021- (2021)

    2021  

    Abstract: Summary: Sharp wave-ripples (SWRs) represent synchronous discharges of hippocampal neurons and are believed to play a major role in memory consolidation. A large body of evidence suggests that SWRs are exclusively generated in the CA3-CA2 network. In ... ...

    Abstract Summary: Sharp wave-ripples (SWRs) represent synchronous discharges of hippocampal neurons and are believed to play a major role in memory consolidation. A large body of evidence suggests that SWRs are exclusively generated in the CA3-CA2 network. In contrast, here, we provide several lines of evidence showing that the subiculum can function as a secondary SWRs generator. SWRs with subicular origin propagate forward into the entorhinal cortex as well as backward into the hippocampus proper. Our findings suggest that the output structures of the hippocampus are not only passively facilitating the transfer of SWRs to the cortex, but they also can actively contribute to the genesis of SWRs. We hypothesize that SWRs with a subicular origin may be important for the consolidation of information conveyed to the hippocampus via the temporoammonic pathway.
    Keywords hippocampus ; CA3 ; CA1 ; subiculum ; entorhinal cortex ; oscillations ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2021-04-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Functional consequences of the disturbances in the GABA-mediated inhibition induced by injuries in the cerebral cortex.

    Imbrosci, Barbara / Mittmann, Thomas

    Neural plasticity

    2011  Volume 2011, Page(s) 614329

    Abstract: Cortical injuries are often reported to induce a suppression of the intracortical GABAergic inhibition in the surviving, neighbouring neuronal networks. Since GABAergic transmission provides the main source of inhibition in the mammalian brain, this ... ...

    Abstract Cortical injuries are often reported to induce a suppression of the intracortical GABAergic inhibition in the surviving, neighbouring neuronal networks. Since GABAergic transmission provides the main source of inhibition in the mammalian brain, this condition may lead to hyperexcitability and epileptiform activity of cortical networks. However, inhibition plays also a crucial role in limiting the plastic properties of neuronal circuits, and as a consequence, interventions aiming to reestablish a normal level of inhibition might constrain the plastic capacity of the cortical tissue. A promising strategy to minimize the deleterious consequences of a modified inhibitory transmission without preventing the potential beneficial effects on cortical plasticity may be to unravel distinct GABAergic signaling pathways separately mediating these positive and negative events. Here, gathering data from several recent studies, we provide new insights to better face with this "double coin" condition in the attempt to optimize the functional recovery of patients.
    MeSH term(s) Brain Injuries/metabolism ; Brain Injuries/physiopathology ; Cerebral Cortex/injuries ; Cerebral Cortex/metabolism ; Cerebral Cortex/physiopathology ; Humans ; Neural Inhibition/physiology ; Neurons/physiology ; Synaptic Transmission/physiology ; gamma-Aminobutyric Acid/metabolism
    Chemical Substances gamma-Aminobutyric Acid (56-12-2)
    Language English
    Publishing date 2011-05-31
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 1454938-4
    ISSN 1687-5443 ; 2090-5904 ; 0792-8483
    ISSN (online) 1687-5443
    ISSN 2090-5904 ; 0792-8483
    DOI 10.1155/2011/614329
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Focal cortical lesions induce bidirectional changes in the excitability of fast spiking and non fast spiking cortical interneurons.

    Imbrosci, Barbara / Neitz, Angela / Mittmann, Thomas

    PloS one

    2014  Volume 9, Issue 10, Page(s) e111105

    Abstract: A physiological brain function requires neuronal networks to operate within a well-defined range of activity. Indeed, alterations in neuronal excitability have been associated with several pathological conditions, ranging from epilepsy to ... ...

    Abstract A physiological brain function requires neuronal networks to operate within a well-defined range of activity. Indeed, alterations in neuronal excitability have been associated with several pathological conditions, ranging from epilepsy to neuropsychiatric disorders. Changes in inhibitory transmission are known to play a key role in the development of hyperexcitability. However it is largely unknown whether specific interneuronal subpopulations contribute differentially to such pathological condition. In the present study we investigated functional alterations of inhibitory interneurons embedded in a hyperexcitable cortical circuit at the border of chronically induced focal lesions in mouse visual cortex. Interestingly, we found opposite alterations in the excitability of non fast-spiking (Non Fs) and fast-spiking (Fs) interneurons in acute cortical slices from injured animals. Non Fs interneurons displayed a depolarized membrane potential and a higher frequency of spontaneous excitatory postsynaptic currents (sEPSCs). In contrast, Fs interneurons showed a reduced sEPSCs amplitude. The observed downscaling of excitatory synapses targeting Fs interneurons may prevent the recruitment of this specific population of interneurons to the hyperexcitable network. This mechanism is likely to seriously affect neuronal network function and to exacerbate hyperexcitability but it may be important to protect this particular vulnerable population of GABAegic neurons from excitotoxicity.
    MeSH term(s) Action Potentials ; Animals ; Cerebral Cortex/cytology ; Cerebral Cortex/injuries ; Cerebral Cortex/physiology ; Excitatory Postsynaptic Potentials ; Interneurons/physiology ; Mice ; Visual Cortex/cytology ; Visual Cortex/physiology
    Language English
    Publishing date 2014-10-27
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0111105
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Physiological Properties of Supragranular Cortical Inhibitory Interneurons Expressing Retrograde Persistent Firing

    Barbara Imbrosci / Angela Neitz / Thomas Mittmann

    Neural Plasticity, Vol

    2015  Volume 2015

    Keywords Medicine ; R ; Internal medicine ; RC31-1245 ; Neurosciences. Biological psychiatry. Neuropsychiatry ; RC321-571
    Publishing date 2015-01-01T00:00:00Z
    Publisher Hindawi Publishing Corporation
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: A Cellular Mechanism Underlying Enhanced Capability for Complex Olfactory Discrimination Learning.

    Chandra, Naveen / Awasthi, Richa / Ozdogan, Togba / Johenning, Friedrich W / Imbrosci, Barbara / Morris, Genela / Schmitz, Dietmar / Barkai, Edi

    eNeuro

    2019  Volume 6, Issue 1

    Abstract: The biological mechanisms underlying complex forms of learning requiring the understanding of rules based on previous experience are not yet known. Previous studies have raised the intriguing possibility that improvement in complex learning tasks ... ...

    Abstract The biological mechanisms underlying complex forms of learning requiring the understanding of rules based on previous experience are not yet known. Previous studies have raised the intriguing possibility that improvement in complex learning tasks requires the long-term modulation of intrinsic neuronal excitability, induced by reducing the conductance of the slow calcium-dependent potassium current (sI
    MeSH term(s) Animals ; Discrimination Learning/physiology ; Excitatory Amino Acid Agonists/pharmacology ; Extracellular Signal-Regulated MAP Kinases/metabolism ; Kainic Acid/pharmacology ; Male ; Maze Learning/physiology ; Membrane Potentials/drug effects ; Membrane Potentials/physiology ; Mice, Inbred C57BL ; Mice, Knockout ; Olfactory Perception/physiology ; Piriform Cortex/drug effects ; Piriform Cortex/physiology ; Protein Kinase C/metabolism ; Pyramidal Cells/drug effects ; Pyramidal Cells/physiology ; Rats, Sprague-Dawley ; Receptors, Kainic Acid/genetics ; Receptors, Kainic Acid/metabolism ; Tissue Culture Techniques ; GluK2 Kainate Receptor
    Chemical Substances Excitatory Amino Acid Agonists ; Receptors, Kainic Acid ; Protein Kinase C (EC 2.7.11.13) ; Extracellular Signal-Regulated MAP Kinases (EC 2.7.11.24) ; Kainic Acid (SIV03811UC)
    Language English
    Publishing date 2019-02-12
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2800598-3
    ISSN 2373-2822 ; 2373-2822
    ISSN (online) 2373-2822
    ISSN 2373-2822
    DOI 10.1523/ENEURO.0198-18.2019
    Database MEDical Literature Analysis and Retrieval System OnLINE

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