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Serotonergic System, Cognition, and BPSD in Alzheimer's Disease

Overview
Journal Neurosci Lett
Specialty Neurology
Date 2019 Apr 5
PMID 30946928
Citations 46
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Abstract

Behavioral and Psychological Symptoms of Dementia (BPSD), present in almost 90% of patients with Alzheimer's Disease (AD), cause extensive impairment leading to reduced independence and inability to complete activities of daily living. Though BPSD includes a wide range of symptoms, such as agitation, aggression, disinhibition, anxiety, depression, apathy, delusions, and hallucinations. Certain BPSD in AD co-present and can be clustered into distinct domains based on their frequency of co-occurrence. As these BPSD are so pervasive in any stages of AD, the disease may be better characterized as a disorder of heterogeneous degenerative symptoms across a number of symptom domains, with the most prominent domain comprising memory and cognitive deficits. Importantly, there are no FDA-approved drugs to treat these BPSD, and new approaches must be considered to develop effective treatments for AD patients. The biogenic monoamine 5-hydroxytryptamine (5-HT), or serotonin, works as both a neurotransmitter and neuromodulator, which has been tied to cognitive decline and multiple BPSD domains. This review summarizes the evidence for specific serotonergic system alterations across some of the well-studied cognitive, behavioral, and psychiatric domains. Though differences in overall serotonergic transmission occur in AD, circuit-specific alterations in individual 5-HT receptors (5-HTRs) are likely linked to the heterogeneous presentation of BPSD in AD.

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References
1.
Glikmann-Johnston Y, Saling M, Reutens D, Stout J . Hippocampal 5-HT1A Receptor and Spatial Learning and Memory. Front Pharmacol. 2015; 6:289. PMC: 4674558. DOI: 10.3389/fphar.2015.00289. View

2.
Vitalis T, Ansorge M, Dayer A . Serotonin homeostasis and serotonin receptors as actors of cortical construction: special attention to the 5-HT3A and 5-HT6 receptor subtypes. Front Cell Neurosci. 2013; 7:93. PMC: 3686152. DOI: 10.3389/fncel.2013.00093. View

3.
Gonda X, Juhasz G, Laszik A, Rihmer Z, Bagdy G . Subthreshold depression is linked to the functional polymorphism of the 5HT transporter gene. J Affect Disord. 2005; 87(2-3):291-7. DOI: 10.1016/j.jad.2005.05.007. View

4.
de Boer S, Koolhaas J . 5-HT1A and 5-HT1B receptor agonists and aggression: a pharmacological challenge of the serotonin deficiency hypothesis. Eur J Pharmacol. 2005; 526(1-3):125-39. DOI: 10.1016/j.ejphar.2005.09.065. View

5.
Tesseur I, Pimenova A, Lo A, Ciesielska M, Lichtenthaler S, De Maeyer J . Chronic 5-HT4 receptor activation decreases Aβ production and deposition in hAPP/PS1 mice. Neurobiol Aging. 2013; 34(7):1779-89. DOI: 10.1016/j.neurobiolaging.2013.01.020. View