Full Text Available

Note: Clicking the button above will open the full text document at the original institutional repository in a new window.

Serotonin receptor mechanisms in anti-depressant action

Bibliography: leaves 221-270.

Saved in:
Bibliographic Details
Main Author: Quested, Digby John
Other Authors: Cowen, Philip
Format: Thesis
Language:English
Published: Department of Psychiatry and Mental Health 2015
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867613170771689472
access_status_str Open Access
author Quested, Digby John
author2 Cowen, Philip
author_browse Cowen, Philip
Quested, Digby John
author_facet Cowen, Philip
Quested, Digby John
author_sort Quested, Digby John
collection Thesis
description Bibliography: leaves 221-270.
format Thesis
id oai:open.uct.ac.za:11427/12577
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:31:53.390Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2015
publishDateRange 2015
publishDateSort 2015
publisher Department of Psychiatry and Mental Health
publisherStr Department of Psychiatry and Mental Health
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/12577 Serotonin receptor mechanisms in anti-depressant action Quested, Digby John Cowen, Philip Psychiatry Bibliography: leaves 221-270. Serotonin neurones have been implicated in the pathophysiology and treatment of clinical depression to a greater degree than any other neurotransmitter. Additionally, serotonin pathways may playa role in the pathophysiology and treatment of eating disorders, anxiety states and schizophrenia. Molecular biological studies have confirmed pharmacological evidence suggesting the existence of multiple serotonin receptor subtypes and the genes for these receptors, as well as that of the serotonin transporter, have common polymorphic variants. To investigate the effect of repeated treatment with selective serotonin fe-uptake inhibitors (SSRI's) on the function of central 5-HT2C receptors. To assess the effect of polymorphic variation in the 5-HT2c receptor and serotonin transporter on functional responses to selective pharmacological challenge. To determine whether polymorphic variation in the 5-HT receptor and serotonin transporter influence the clinical response of patients with major depression to treatment with serotonergic antidepressants. To assess the effect of repeated treatment with selective serotonin re-uptake inhibitors (SSRI's) on the function of central 5-HT2c receptors I used the 5-HT2C receptor agonist, m-chlorophenylpiperazine (m-CPP) as a 5-HT2c probe in a neuroendocrine challenge paradigm. I used the same approach to assess whether polymorphic variation in the 5-HT2c receptor (serine vs cysteine substitution) was associated with differences in functional response to 5-HT2C receptor challenge. I then studied whether polymorphic variation in the serotonin transporter promotor region (long versus short form) was associated with differing functional responses to acute challenge with clomipramine, a tricyclic antidepressant with a high affinity for the serotonin transporter. Finally, I studied whether either of these polymorphic variants influenced the clinical response of patients with major depression to treatment with SSRI's and clomipramine. SSRI treatment significantly lowered the sensitivity of 5-HT2c receptors as predicted from animal experimental studies. However polymorphic variation in the 5-HTzc receptor did not significantly influence functional responses to m-CPP challenge. In contrast polymorphic variation in the serotonin transporter was associated with differing neuroendocrine responses to acute clomipramine challenge with greater prolactin release being seen in subjects with the long polymorphic variant. Neither the 5-HTzc nor the transporter polymorphisms correlated with clinical response to SSRI and clomipramine treatment in patients with major depression. The ability of SSRI's to produce a functional down-regulation of 5-HTzc receptors may be relevant to certain of their therapeutic effects. Polymorphic variation in the 5-HT2c receptor (serine vs cysteine) seems unlikely to explain functional differences in responses to 5-HTzc receptor challenge or antidepressant responses to SSRI treatment. In contrast variation in the serotonin transporter promotor is associated with differing functional responses to acute serotonin re-uptake blockade. However, this did not correlate with clinical response to longer-term SSRI treatment. 2015-03-04T19:28:15Z 2015-03-04T19:28:15Z 2003 Master Thesis Masters MD http://hdl.handle.net/11427/12577 eng application/pdf Department of Psychiatry and Mental Health Faculty of Health Sciences University of Cape Town
spellingShingle Psychiatry
Quested, Digby John
Serotonin receptor mechanisms in anti-depressant action
thesis_degree_str Master's
title Serotonin receptor mechanisms in anti-depressant action
title_full Serotonin receptor mechanisms in anti-depressant action
title_fullStr Serotonin receptor mechanisms in anti-depressant action
title_full_unstemmed Serotonin receptor mechanisms in anti-depressant action
title_short Serotonin receptor mechanisms in anti-depressant action
title_sort serotonin receptor mechanisms in anti depressant action
topic Psychiatry
url http://hdl.handle.net/11427/12577
work_keys_str_mv AT questeddigbyjohn serotoninreceptormechanismsinantidepressantaction