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  • 1
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 1994
    In:  NeuroReport Vol. 5, No. 14 ( 1994-09), p. 1813-1816
    In: NeuroReport, Ovid Technologies (Wolters Kluwer Health), Vol. 5, No. 14 ( 1994-09), p. 1813-1816
    Type of Medium: Online Resource
    ISSN: 0959-4965
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 1994
    detail.hit.zdb_id: 2031485-1
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2016
    In:  European Journal of Neuroscience Vol. 43, No. 12 ( 2016-06), p. 1535-1552
    In: European Journal of Neuroscience, Wiley, Vol. 43, No. 12 ( 2016-06), p. 1535-1552
    Abstract: In the last few years, a rapidly growing number of autoantibodies targeting neuronal cell‐surface antigens have been identified in patients presenting with neurological symptoms. Targeted antigens include ionotropic receptors such as N ‐methyl‐ d ‐aspartate receptor or the α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid receptor, metabotropic receptors such as mG luR1 and mG luR5, and other synaptic proteins, some of them belonging to the voltage‐gated potassium channel complex. Importantly, the cell‐surface location of these antigens makes them vulnerable to direct antibody‐mediated modulation. Some of these autoantibodies, generally targeting ionotropic channels or their partner proteins, define clinical syndromes resembling models of pharmacological or genetic disruption of the corresponding antigen, suggesting a direct pathogenic role of the associated autoantibodies. Moreover, the associated neurological symptoms are usually immunotherapy‐responsive, further arguing for a pathogenic effect of the antibodies. Some studies have shown that some patients’ antibodies may have structural and functional in vitro effects on the targeted antigens. Definite proof of the pathogenicity of these autoantibodies has been obtained for just a few through passive transfer experiments in animal models. In this review we present existing and converging evidence suggesting a pathogenic role of some autoantibodies directed against neuronal cell‐surface antigens observed in patients with central nervous system disorders. We describe the main clinical symptoms characterizing the patients and discuss conflicting arguments regarding the pathogenicity of these antibodies.
    Type of Medium: Online Resource
    ISSN: 0953-816X , 1460-9568
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2016
    detail.hit.zdb_id: 2005178-5
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    Society for Neuroscience ; 2008
    In:  The Journal of Neuroscience Vol. 28, No. 8 ( 2008-02-20), p. 1804-1815
    In: The Journal of Neuroscience, Society for Neuroscience, Vol. 28, No. 8 ( 2008-02-20), p. 1804-1815
    Abstract: Noradrenergic modulation of cortical circuits is involved in information processing, regulation of higher functions, and prevention of epileptic activity. Here, we studied the effects of noradrenaline on the functional connectivity of GABAergic networks of the hippocampus and show that electrical synapses between interneurons are a novel target of noradrenergic modulation in vitro . Application of noradrenaline or of the selective β-adrenergic agonist isoproterenol decreased gap junction-based coupling in paired recordings from stratum lacunosum-moleculare interneurons by ∼40%. Similar results were obtained after pharmacological stimulation of the adenylyl cyclase with forskolin. In contrast, the adenylyl cyclase antagonist MDL12330A [ cis-N -(2-phenylcyclopentyl)azacyclotridec-1-en-2-amine] or the specific protein kinase A (PKA) inhibitor H89 ( N -[2-( p -bromocinnamyl-amino)ethyl]-5-isoquinolinesulfonamide dihydrochloride) enhanced the basal strength of coupling by ∼30%. In addition, PKA-mediated phosphorylation was critical for both isoproterenol- and forskolin-dependent regulation of coupling, because inclusion of the PKA antagonist KT5720 [(9 S ,10 R ,12 R )-2,3,9,10,11,12-hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1 H -diindolo[1,2,3-fg:3′,2′,1′-kl]pyrrolo[3,4-i] [1,6]benzodiazocine-10-carboxylicacid hexyl ester] in the recording pipettes prevented modulation. Lastly, we studied the effects of β-adrenergic modulation on mixed polysynaptic transmission within the GABAergic network. Isoproterenol depressed propagation of GABA A receptor-mediated synaptic currents, but did not change significantly direct GABAergic input, indicating that regulation of electrical coupling adds flexibility to the information flow generated by chemical synapses. In conclusion, activation of β-adrenergic receptors in stratum lacunosum-moleculare GABAergic networks reduces electrical synaptic transmission via a cAMP/PKA signaling cascade, and affects the degree of synaptic divergence within the circuit. We propose that this dynamic modulation and interplay between electrical and chemical synaptic transmission in GABAergic networks contributes to the tuning of memory processes in vivo , and prevents hypersynchronous activity.
    Type of Medium: Online Resource
    ISSN: 0270-6474 , 1529-2401
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2008
    detail.hit.zdb_id: 1475274-8
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Society for Neuroscience ; 2005
    In:  The Journal of Neuroscience Vol. 25, No. 38 ( 2005-09-21), p. 8686-8695
    In: The Journal of Neuroscience, Society for Neuroscience, Vol. 25, No. 38 ( 2005-09-21), p. 8686-8695
    Abstract: Electrical coupling among GABAergic interneurons is believed to play an essential role in shaping synchronized brain network activity related to cognition and behavior. We have studied the rules governing the electrical coupling between hippocampal interneurons located in stratum lacunosum-moleculare of the CA1 hippocampus. The most frequently recorded interneuron subtype had short multipolar dendrites and a dense local axonal arborization, typical of neurogliaform cells. Electrical excitability in this class of interneurons was heterogeneous. Although injection of small current steps evoked late spiking, larger steps triggered different types of firing patterns. Trains of action potentials ranged from clearly adapting to highly irregular, with clustered or mostly regular spikes. Electrotonic and action potentials could be propagated to the coupled cells; the coupling coefficient for electrotonic signals was 0.035, which compared with 0.005 for action potentials. Electrical coupling was reversibly blocked by application of carbenoxolone. Multiple simultaneous recordings indicated that interneurons with similar and different firing patterns were electrically coupled. This visual impression was quantitatively confirmed by principal component analysis applied to variables related to membrane excitability. In fact, the probability of finding electrically coupled neurons in our sample was not dependent on the excitable properties of the cells tested and was ∼0.34. The presence of diffuse electrical coupling among hippocampal interneurons of stratum lacunosum-moleculare with different excitability is a novel finding with important implications. For example, the promiscuity of electrical connections may endow inhibitory networks with a large degree of flexibility and regulate the computational power of the hippocampus during different synchronized states.
    Type of Medium: Online Resource
    ISSN: 0270-6474 , 1529-2401
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2005
    detail.hit.zdb_id: 1475274-8
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    Society for Neuroscience ; 2002
    In:  The Journal of Neuroscience Vol. 22, No. 13 ( 2002-07-01), p. 5462-5472
    In: The Journal of Neuroscience, Society for Neuroscience, Vol. 22, No. 13 ( 2002-07-01), p. 5462-5472
    Type of Medium: Online Resource
    ISSN: 0270-6474 , 1529-2401
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2002
    detail.hit.zdb_id: 1475274-8
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    Society for Neuroscience ; 2020
    In:  eneuro Vol. 7, No. 1 ( 2020-01), p. ENEURO.0516-19.2019-
    In: eneuro, Society for Neuroscience, Vol. 7, No. 1 ( 2020-01), p. ENEURO.0516-19.2019-
    Abstract: The study of brain circuits depends on a clear understanding of the role played by different neuronal populations. Therefore, the unambiguous identification of different cell types is essential for the correct interpretation of experimental data. Here, we emphasize to the broader neuroscience community the importance of recognizing the persistent presence of Cajal–Retzius cells in the molecular layers of the postnatal hippocampus, and then we suggest a variety of criteria for distinguishing Cajal–Retzius cells from other neurons of the hippocampal molecular layers, such as GABAergic interneurons and semilunar granule cells. The toolbox of criteria that we have investigated (in male and female mice) can be useful both for anatomical and functional experiments, and relies on the quantitative study of neuronal somatic/nuclear morphology, location and developmental profile, expression of specific molecular markers (GAD67, reelin, COUP-TFII, calretinin, and p73), single cell anatomy, and electrophysiological properties. We conclude that Cajal–Retzius cells are small, non-GABAergic neurons that are tightly associated with the hippocampal fissure (HF), and that, within this area of interest, selectively express the proteins p73 and calretinin. We highlight the dangers of using markers such as reelin or COUP-TFII to identify Cajal–Retzius cells or GABAergic interneurons because of their poor specificity. Lastly, we examine neurons of the postnatal hippocampal molecular layers and show cell type-specific differences in their dendritic/axonal morphologies and density distributions, as well as in their membrane properties and spontaneous synaptic inputs. These parameters can be used to distinguish biocytin-filled and/or electrophysiologically recorded neurons and should be considered to avoid interpretational mistakes.
    Type of Medium: Online Resource
    ISSN: 2373-2822
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2020
    detail.hit.zdb_id: 2800598-3
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  • 7
    Online Resource
    Online Resource
    Elsevier BV ; 2022
    In:  Cell Reports Vol. 39, No. 7 ( 2022-05), p. 110822-
    In: Cell Reports, Elsevier BV, Vol. 39, No. 7 ( 2022-05), p. 110822-
    Type of Medium: Online Resource
    ISSN: 2211-1247
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2022
    detail.hit.zdb_id: 2649101-1
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  • 8
    In: The Journal of Physiology, Wiley, Vol. 587, No. 23 ( 2009-12-01), p. 5691-5708
    Type of Medium: Online Resource
    ISSN: 0022-3751
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2009
    detail.hit.zdb_id: 1475290-6
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    Wiley ; 2011
    In:  The Journal of Physiology Vol. 589, No. 8 ( 2011-04), p. 1873-1874
    In: The Journal of Physiology, Wiley, Vol. 589, No. 8 ( 2011-04), p. 1873-1874
    Type of Medium: Online Resource
    ISSN: 0022-3751
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2011
    detail.hit.zdb_id: 1475290-6
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    Wiley ; 2018
    In:  The Journal of Physiology Vol. 596, No. 16 ( 2018-08), p. 3739-3758
    In: The Journal of Physiology, Wiley, Vol. 596, No. 16 ( 2018-08), p. 3739-3758
    Abstract: By taking advantage of calcium imaging and electrophysiology, we provide direct pharmacological evidence for the functional expression of TRPV1 channels in hippocampal Cajal‐Retzius cells. Application of the TRPV1 activator capsaicin powerfully enhances spontaneous synaptic transmission in the hippocampal layers that are innervated by the axons of Cajal‐Retzius cells. Capsaicin‐triggered calcium responses and membrane currents in Cajal‐Retzius cells, as well as layer‐specific modulation of spontaneous synaptic transmission, are absent when the drug is applied to slices prepared from TRPV1 − / − animals. We discuss the implications of the functional expression of TRPV1 channels in Cajal‐Retzius cells and of the observed TRPV1‐dependent layer‐specific modulation of synaptic transmission for physiological and pathological network processing.
    Type of Medium: Online Resource
    ISSN: 0022-3751 , 1469-7793
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2018
    detail.hit.zdb_id: 1475290-6
    SSG: 12
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