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Principal
Investigator: Cindy L.
Ehlers, PhD
EEG and ERP Measures of Alcohol's Effects
Grant #: NIAAA 06059
The overall goal of this
research program is to utilize electrophysiological measures,
specifically waking EEG, event-related potentials (ERPs),
and measures of the sleep EEG to explore the neural substrates
which underlie alcohol’s abuse liability. Our studies,
as well as others, suggest in human subjects that specific
ERP and sleep/waking EEG measures may be particularly valuable
in: 1) characterizing risk for the future development of
alcoholism 2) exploring individual differences in acute
response to ethanol and 3) quantifying the effects of chronic
ethanol exposure/relapse to drinking. The newly proposed
studies will use electrophysiological measures to further
explore the functional activity of specific brain sites
identified in previous studies, a neural circuit that includes
frontal cortex, the extended amygdala and the hypothalamus,
with ethanol self-administration. Neuropharmacological studies
will be aimed at further understanding neuropeptide modulation
of alcohol consumption as well as the effects of ethanol
exposure on electrophysiological measures of sleep and behavior.
The overall goals of the current research program will be
accomplished through the following specific aims: AIM 1:
To continue to develop clinically relevant electrophysiological
and behavioral measures in rodents which are informative
assays of brain differences between rodent lines that differ
in ethanol preference. AIM 2: To investigate functional
brain electrophysiology in discrete cortical and subcortical
areas during ethanol self-administration with a focus on
determining specific peptidergic influences on alcohol consumption
patterns. AIM 3: To determine the consequences of chronic
ethanol exposure on electrophysiology in rodents with a
specific focus on neurophysiological changes during sleep
and their relation to relapse. The use of these electrophysiological
measures, combined with neurochemical findings will provide
data necessary to directly link these peptidergic systems
to alcohol preference and long term neuroadaption to alcohol.
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