Literature DB >> 7745443

Parvalbumin-immunoreactive neurons in the entorhinal cortex of the rat: localization, morphology, connectivity and ultrastructure.

F G Wouterlood1, W Härtig, G Brückner, M P Witter.   

Abstract

We studied the distribution, morphology, ultrastructure and connectivity of parvalbumin-immunoreactive neurons in the entorhinal cortex of the rat. Immunoreactive cell bodies were found in all layers of the entorhinal cortex except layer I. The highest numbers were observed in layers II and III of the dorsal division of the lateral entorhinal area whereas the lowest numbers occurred in the ventral division of the lateral entorhinal area. Most such neurons displayed multipolar configurations with smooth dendrites. We distinguished a type with long dendrites and a type with short dendrites. We also observed pyramidal immunoreactive neurons. A dense plexus of immunoreactive dendrites and axons was prominent in layers II and III of the dorsal division of the lateral entorhinal area and the medial entorhinal area. None of the parvalbumin-immunoreactive cells became retrogradely labelled after injection of horseradish peroxidase into the hippocampal formation. By electron microscopy, immunoreactivity was observed in cell bodies, dendrites, myelinated and unmyelinated axons and axon terminals. Immunoreactive dendrites and axons occurred in all cortical layers. We noted many myelinated immunoreactive axons. Immunoreactive axon terminals were medium sized, contained pleomorphic synaptic vesicles, and established symmetrical synapses. Both horseradish peroxidase labelled and unlabelled immunonegative cell bodies often received synapses from immunopositive axon terminals arranged in baskets. Synapses between immunoreactive axon terminals and unlabelled dendritic shafts and spines were abundant. Synapses with initial axon segments occurred less frequently. In addition, synaptic contacts were present between immunopositive axon terminals and cell bodies and dendrites. Thus, the several types of parvalbumin-containing neuron in the entorhinal cortex are interneurons, connected to one another and to immunonegative neurons through a network of synaptic contacts. Immunonegative cells projecting to the hippocampal formation receive axo-somatic basket synapses from immunopositive terminals. This connectivity may form the morphological substrate underlying the reported strong inhibition of cells in layers II and III of the entorhinal cortex projecting to the hippocampal formation.

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Year:  1995        PMID: 7745443     DOI: 10.1007/BF01181556

Source DB:  PubMed          Journal:  J Neurocytol        ISSN: 0300-4864


  34 in total

1.  Evidence for spatial modules mediated by temporal synchronization of carbachol-induced gamma rhythm in medial entorhinal cortex.

Authors:  C T Dickson; G Biella; M de Curtis
Journal:  J Neurosci       Date:  2000-10-15       Impact factor: 6.167

2.  Grid cells in pre- and parasubiculum.

Authors:  Charlotte N Boccara; Francesca Sargolini; Veslemøy Hult Thoresen; Trygve Solstad; Menno P Witter; Edvard I Moser; May-Britt Moser
Journal:  Nat Neurosci       Date:  2010-07-25       Impact factor: 24.884

3.  Muscarinic induction of synchronous population activity in the entorhinal cortex.

Authors:  C T Dickson; A Alonso
Journal:  J Neurosci       Date:  1997-09-01       Impact factor: 6.167

4.  Modeling of entorhinal cortex and simulation of epileptic activity: insights into the role of inhibition-related parameters.

Authors:  Etienne Labyt; Paul Frogerais; Laura Uva; Jean-Jacques Bellanger; Fabrice Wendling
Journal:  IEEE Trans Inf Technol Biomed       Date:  2007-07

Review 5.  Background synaptic activity in rat entorhinal cortical neurones: differential control of transmitter release by presynaptic receptors.

Authors:  Roland S G Jones; Gavin L Woodhall
Journal:  J Physiol       Date:  2004-10-21       Impact factor: 5.182

6.  GABAergic presubicular projections to the medial entorhinal cortex of the rat.

Authors:  T van Haeften; F G Wouterlood; B Jorritsma-Byham; M P Witter
Journal:  J Neurosci       Date:  1997-01-15       Impact factor: 6.167

7.  Presubicular and parasubicular cortical neurons of the rat: functional separation of deep and superficial neurons in vitro.

Authors:  M Funahashi; M Stewart
Journal:  J Physiol       Date:  1997-06-01       Impact factor: 5.182

8.  Feedforward inhibition regulates perirhinal transmission of neocortical inputs to the entorhinal cortex: ultrastructural study in guinea pigs.

Authors:  Aline Pinto; Cesar Fuentes; Denis Paré
Journal:  J Comp Neurol       Date:  2006-04-20       Impact factor: 3.215

9.  Layer-specific modulation of entorhinal cortical excitability by presubiculum in a rat model of temporal lobe epilepsy.

Authors:  Saad Abbasi; Sanjay S Kumar
Journal:  J Neurophysiol       Date:  2015-09-16       Impact factor: 2.714

10.  Network hyperexcitability within the deep layers of the pilocarpine-treated rat entorhinal cortex.

Authors:  Philip de Guzman; Yuji Inaba; Enrica Baldelli; Marco de Curtis; Giuseppe Biagini; Massimo Avoli
Journal:  J Physiol       Date:  2008-01-31       Impact factor: 5.182

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