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      Effects of serotonin in the hippocampus: how SSRIs and multimodal antidepressants might regulate pyramidal cell function

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          Abstract

          The hippocampus plays an important role in emotional and cognitive processing, and both of these domains are affected in patients with major depressive disorder (MDD). Extensive preclinical research and the notion that modulation of serotonin (5-HT) neurotransmission plays a key role in the therapeutic efficacy of selective serotonin reuptake inhibitors (SSRIs) support the view that 5-HT is important for hippocampal function in normal and disease-like conditions. The hippocampus is densely innervated by serotonergic fibers, and the majority of 5-HT receptor subtypes are expressed there. Furthermore, hippocampal cells often co-express multiple 5-HT receptor subtypes that can have either complementary or opposing effects on cell function, adding to the complexity of 5-HT neurotransmission. Here we review the current knowledge of how 5-HT, through its various receptor subtypes, modulates hippocampal output and the activity of hippocampal pyramidal cells in rodents. In addition, we discuss the relevance of 5-HT modulation for cognitive processing in rodents and possible clinical implications of these results in patients with MDD. Finally, we review the data on how SSRIs and vortioxetine, an antidepressant with multimodal activity, affect hippocampal function, including cognitive processing, from both a preclinical and clinical perspective.

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          Interneurons of the hippocampus.

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            Long-axis specialization of the human hippocampus.

            Investigation of the hippocampus has historically focused on computations within the trisynaptic circuit. However, discovery of important anatomical and functional variability along its long axis has inspired recent proposals of long-axis functional specialization in both the animal and human literatures. Here, we review and evaluate these proposals. We suggest that various long-axis specializations arise out of differences between the anterior (aHPC) and posterior hippocampus (pHPC) in large-scale network connectivity, the organization of entorhinal grid cells, and subfield compositions that bias the aHPC and pHPC towards pattern completion and separation, respectively. The latter two differences give rise to a property, reflected in the expression of multiple other functional specializations, of coarse, global representations in anterior hippocampus and fine-grained, local representations in posterior hippocampus. Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.
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              Regional dissociations within the hippocampus--memory and anxiety.

              The amnestic effects of hippocampal lesions are well documented, leading to numerous memory-based theories of hippocampal function. It is debatable, however, whether any one of these theories can satisfactorily account for all the consequences of hippocampal damage: Hippocampal lesions also result in behavioural disinhibition and reduced anxiety. A growing number of studies now suggest that these diverse behavioural effects may be associated with different hippocampal subregions. There is evidence for at least two distinct functional domains, although recent neuroanatomical studies suggest this may be an underestimate. Selective lesion studies show that the hippocampus is functionally subdivided along the septotemporal axis into dorsal and ventral regions, each associated with a distinct set of behaviours. Dorsal hippocampus has a preferential role in certain forms of learning and memory, notably spatial learning, but ventral hippocampus may have a preferential role in brain processes associated with anxiety-related behaviours. The latter's role in emotional processing is also distinct from that of the amygdala, which is associated specifically with fear. Gray and McNaughton's theory can in principle incorporate these apparently distinct hippocampal functions, and provides a plausible unitary account for the multiple facets of hippocampal function.
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                Author and article information

                Journal
                CNS Spectr
                CNS Spectr
                CNS
                CNS Spectrums
                Cambridge University Press (New York, USA )
                1092-8529
                08 September 2015
                April 2016
                : 21
                : 2
                : 143-161
                Affiliations
                [1 ]Lundbeck Research USA, Paramus, New Jersey, USA
                [2 ]Lundbeck DK, Copenhagen-Valby, Denmark
                Author notes
                [* ]Address for correspondence: Elena Dale, PhD, Lundbeck Research USA, 215 College Rd., Paramus, NJ 07652, USA. (Email: EDAL@ 123456lundbeck.com )
                Article
                S1092852915000425 00042
                10.1017/S1092852915000425
                4825106
                26346726
                b62601e4-5264-4c73-83ff-c79e6a1e2047
                © Cambridge University Press 2015

                The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence < http://creativecommons.org/licenses/by-nc-sa/3.0/>. The written permission of Cambridge University Press must be obtained for commercial re-use.

                History
                : 06 March 2015
                : 03 June 2015
                Page count
                Figures: 2, Tables: 2, Pages: 19
                Categories
                Review Articles

                hippocampus,pyramidal cell,serotonin,ssri,vortioxetine
                hippocampus, pyramidal cell, serotonin, ssri, vortioxetine

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