Back to results

Washington University in St. Louis

Serotonergic Signaling Pathways that Suppress Amyloid Beta in Mouse Models of AD

Abstract

dc:description.abstract

<p>A diagnosis of Alzheimer's disease is one of the most devastating things one can hear. This terrible disease robs people of their ability to remember cherished events as their brains become riddled with beta amyloid plaques. Alzheimer's is especially terrifying because there currently are no effective treatments for slowing or stopping the disease. However, recent research has shown that plaque formation is correlated to concentrations of amyloid beta. This discovery suggests that limiting amyloid beta production could potentially halt the disease. One promising avenue for slowing amyloid beta production is serotonergic signaling.</p> <p>This dissertation presents evidence for a direct sequence of signaling events from serotonin receptors to reduction of amyloid beta by alpha-secretase. Two serotonin receptors, 5-HT4R and 5-HT7R, reduce amyloid beta levels in the brains of transgenic mice that model Alzheimer's disease. These receptors are linked to activation of PKA, and blocking PKA activity increases amyloid levels in mice. PKA leads to activation of ERK, a kinase which acts in both the nucleus and the cytoplasm. We show SSRI antidepressant treatment fails to produce changes in gene expression which suggests ERK acts within the cytoplasm to reduce amyloid beta. Finally, we show that selective inhibition of ADAM10, the primary alpha-secretase, is unable to block the beneficial effects of SSRI antidepressants in transgenic mice. These discoveries explain the mechanisms regulating amyloid beta reduction by serotonin activity and also offer a more selective therapy for Alzheimer's disease.</p>

Degree

thesis:*
Name thesis:degree_name
Doctor of Philosophy (PhD)
Level thesis:degree_level
Dissertation
Discipline thesis:degree_discipline
Biology and Biomedical Sciences: Molecular Cell Biology
Year dc:date.available
2014

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Fisher, Jonathan Robert
Contributors dc:contributor
  • John R Cirrito

Subjects

dc:subject × 7

Rights

Language dc:language
English (en)

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:openscholarship.wustl.edu:etd-2301

Chain of custody

source
Harvested from
Washington University in St. Louis
Base URL
openscholarship.wustl.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Fisher, Jonathan Robert. Serotonergic Signaling Pathways that Suppress Amyloid Beta in Mouse Models of AD. Dissertation thesis, 2014. https://openscholarship.wustl.edu/etd/1301