The University of Southampton
University of Southampton Institutional Repository

An analysis of ethanol-induced behavioural plasticity in Caenorhabditis elegans

Mitchell, Philippa Helen (2009) An analysis of ethanol-induced behavioural plasticity in Caenorhabditis elegans University of Southampton Doctoral Thesis , 348pp.

Record type: Thesis (Doctoral)


Ethanol is one of the most widely used and socially acceptable drugs in the world.
However its chronic use can lead to serious problems including the development of
dependence. Alcohol dependence is a chronic, relapsing disorder characterised by
tolerance, withdrawal, preoccupation with obtaining alcohol, loss of control over its
consumption and impairment in social and occupational functioning. In humans this
develops over years, primarily driven by adaptations in many distinct signalling
pathways and neural circuits as a result of continued heavy drinking. Whilst alcohol
dependence has been extensively studied our understanding of how its distinct targets
integrate to produce various behavioural responses remains far from clear.

The nematode worm Caenorhabditis elegans is a model genetic organism with a
simple nervous system and well-defined behaviour. These nematodes can display
plasticity in the form of tolerance to, and withdrawal from, 5-HT or nicotine. They are
thus a genetically tractable system in which to investigate the neural substrates of
adaptive responses to ethanol. In this simple system the impact of changes at the
molecular level on signalling in defined neural circuits and the resultant animal
behaviour can be investigated. The aims of this thesis were to establish a C. elegans
paradigm for alcohol dependence and to use this to define the genetic basis of the
ethanol-dependent behaviours of intoxication, tolerance and withdrawal.

Evidence was provided that ethanol equilibrates rapidly across the worm cuticle
indicating that the internal concentration closely approximates to the external
concentration in which the animal is placed. Ethanol-dependent behaviours were
carefully characterised using a variety of behavioural assays. C. elegans exhibit
distinct behavioural states, corresponding to intoxication and withdrawal, which
impair the ability to navigate towards food. Visual and automated analysis defined a
sub-behaviour, an increased tendency to form spontaneous deep body bends, which
was specifically associated with withdrawal. This was ameliorated by a low dose of
alcohol supporting the contention that it arises from ethanol-induced neuroadaptation.

A series of loss of function mutants, were analysed for alterations in ethanoldependent
behaviour. The absence of withdrawal in a strain of worms depleted in
neuropeptides (egl-3) demonstrated that peptidergic signalling is key to the chronic
adaption to, but not to the acute effects of, ethanol. However the neuropeptide
receptor NPR-1, previously shown to impact on ethanol responses in C. elegans, had
no effect on withdrawal behaviour in these assays. Alterations in intoxication and
withdrawal behaviour in strains of worms depleted in 5-HT (tph-1) and dopamine
(cat-2) indicated that serotonergic and dopaminergic signalling may also be involved
in the ethanol response in C. elegans. This study has therefore provided a quantitative
analysis of distinct ethanol-induced behavioural states and highlighted a role for
neuropeptides and major classes of neuromodulatory transmitters. In particular this
data is consistent with the emerging role of neuropeptides in ethanol withdrawal.

PDF Philippa_Mitchell_-_thesis.pdf - Other
Download (2MB)

More information

Published date: 28 September 2009
Organisations: University of Southampton


Local EPrints ID: 159713
PURE UUID: e455cc0b-140b-4ed5-be6c-e4657f728e1a

Catalogue record

Date deposited: 16 Jul 2010 11:41
Last modified: 18 Jul 2017 12:37

Export record


Author: Philippa Helen Mitchell
Thesis advisor: Linda Holden-Dye
Thesis advisor: Vincent O'connor

University divisions

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton:

ePrints Soton supports OAI 2.0 with a base URL of

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.