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      Modulation of Hippocampal Circuits by Muscarinic and Nicotinic Receptors

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          Abstract

          This article provides a review of the effects of activation of muscarinic and nicotinic receptors on the physiological properties of circuits in the hippocampal formation. Previous articles have described detailed computational hypotheses about the role of cholinergic neuromodulation in enhancing the dynamics for encoding in cortical structures and the role of reduced cholinergic modulation in allowing consolidation of previously encoded information. This article will focus on addressing the broad scope of different modulatory effects observed within hippocampal circuits, highlighting the heterogeneity of cholinergic modulation in terms of the physiological effects of activation of muscarinic and nicotinic receptors and the heterogeneity of effects on different subclasses of neurons.

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          Most cited references204

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          Interneurons of the hippocampus.

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            The θ-γ neural code.

            Theta and gamma frequency oscillations occur in the same brain regions and interact with each other, a process called cross-frequency coupling. Here, we review evidence for the following hypothesis: that the dual oscillations form a code for representing multiple items in an ordered way. This form of coding has been most clearly demonstrated in the hippocampus, where different spatial information is represented in different gamma subcycles of a theta cycle. Other experiments have tested the functional importance of oscillations and their coupling. These involve correlation of oscillatory properties with memory states, correlation with memory performance, and effects of disrupting oscillations on memory. Recent work suggests that this coding scheme coordinates communication between brain regions and is involved in sensory as well as memory processes. Copyright © 2013 Elsevier Inc. All rights reserved.
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              Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons.

              An understanding of the diversity of cortical GABAergic interneurons is critical to understand the function of the cerebral cortex. Recent data suggest that neurons expressing three markers, the Ca2+-binding protein parvalbumin (PV), the neuropeptide somatostatin (SST), and the ionotropic serotonin receptor 5HT3a (5HT3aR) account for nearly 100% of neocortical interneurons. Interneurons expressing each of these markers have a different embryological origin. Each group includes several types of interneurons that differ in morphological and electrophysiological properties and likely have different functions in the cortical circuit. The PV group accounts for ∼40% of GABAergic neurons and includes fast spiking basket cells and chandelier cells. The SST group, which represents ∼30% of GABAergic neurons, includes the Martinotti cells and a set of neurons that specifically target layerIV. The 5HT3aR group, which also accounts for ∼30% of the total interneuronal population, is heterogeneous and includes all of the neurons that express the neuropeptide VIP, as well as an equally numerous subgroup of neurons that do not express VIP and includes neurogliaform cells. The universal modulation of these neurons by serotonin and acetylcholine via ionotropic receptors suggests that they might be involved in shaping cortical circuits during specific brain states and behavioral contexts. Copyright © 2010 Wiley Periodicals, Inc.
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                Author and article information

                Contributors
                Journal
                Front Neural Circuits
                Front Neural Circuits
                Front. Neural Circuits
                Frontiers in Neural Circuits
                Frontiers Media S.A.
                1662-5110
                13 December 2017
                2017
                : 11
                : 102
                Affiliations
                [1]Center for Systems Neuroscience, Department of Psychological and Brain Sciences, Boston University , Boston, MA, United States
                Author notes

                Edited by: Oscar Herreras, Consejo Superior de Investigaciones Científicas (CSIC), Spain

                Reviewed by: Jerrel Yakel, National Institute of Environmental Health Sciences (NIH), United States; Heiko J. Luhmann, Johannes Gutenberg-Universität Mainz, Germany

                *Correspondence: Holger Dannenberg hdannenb@ 123456gmail.com
                Article
                10.3389/fncir.2017.00102
                5733553
                29321728
                f4cb93df-cf9f-4ce5-b48e-622642b70e7f
                Copyright © 2017 Dannenberg, Young and Hasselmo.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 01 October 2017
                : 27 November 2017
                Page count
                Figures: 1, Tables: 0, Equations: 0, References: 230, Pages: 18, Words: 16805
                Funding
                Funded by: National Institutes of Health 10.13039/100000002
                Award ID: MH060013, MH061492
                Funded by: Office of Naval Research 10.13039/100000006
                Award ID: N00014-16-1-2832
                Categories
                Neuroscience
                Review

                Neurosciences
                acetylcholine,presynaptic inhibition,tonic depolarization,cholinergic fibers,volume transmission

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