The Effect of Ethanol on Brain Activity
| Status: | Completed |
|---|---|
| Conditions: | Healthy Studies |
| Therapuetic Areas: | Other |
| Healthy: | No |
| Age Range: | 21 - 45 |
| Updated: | 11/24/2018 |
| Start Date: | December 9, 2003 |
| End Date: | December 17, 2012 |
The Effect of Ethanol on Cerebral Blood Flow as Measured by Functional Magnetic Resonance Imaging and the Development of Conditioned Response to Ethanol Administration
This study is divided into two parts; each designed to answer a separate but related
question:
Which brain regions are activated in humans by the rewarding properties of ethanol
administration?
Is it possible to demonstrate a conditioned response to a stimulus paired with rising blood
alcohol concentrations (BAC) in humans and can this response be observed in the brain using
functional magnetic resonance images (fMRI) techniques?
Part 1. In order to determine which brain regions are activated by the rewarding properties
of ethanol administration, we propose to use Blood Oxygenation Level Dependent (BOLD) fMRI
techniques to test the hypothesis that during the time of rising and peak BAC, mesolimbic,
mesocortical, and nigrostriatal dopamine (DA) terminal areas of the brain will show
significant increases in cerebral blood flow. Healthy, non-alcoholic subjects will be given
intravenous (IV) ethanol or placebo infusions on separate days. The infusions will have three
phases. On each day, during the first phase a saline infusion will be used to measure basal
brain blood flow. The second phase will be an ethanol infusion delivered at rates calculated
to produce a BAC of 0.08 plus or minus 0.005 g/dl at 10 minutes. The rate of the infusion for
the next 10 minutes (third phase) will be calculated to maintain BAC at the target level of
0.08 plus or minus 0.005 g/dl for the duration of the infusion. On the placebo day, subjects
will receive a saline infusion at the same set of rates for phases two and three as used
during their ethanol infusion. Continuous multi-slice fMRI data will be collected during each
infusion.
Part 2. In order to investigate conditioned response to ethanol, three groups of healthy,
non-alcoholic subjects will be given a series of IV infusions on separate days. The
experimental group will receive ethanol infusion paired with a conditioned stimulus (CS)
which will be presented while the BAC is rising. One control group (I) of healthy,
non-alcoholic subjects will also be given a series of intravenous ethanol infusions on
separate days, but these infusions will not be paired with a CS. The other control group (II)
will be given only saline infusions during the CS presentation. After three training
sessions, all three groups will undergo an fMRI scan during which the CS will be paired with
saline infusion. This will allow the response to the CS alone to be observed. After 10
minutes of CS presentation, the ethanol infusion will begin and continue for another 15
minutes. Conditioned response (CR) will be demonstrated if the experimental group shows
greater increase in BOLD signal than the control groups in motivation areas such as
mesolimbic, mesocortical, and nigrostriatal dopamine (DA) terminal areas of the brain in
response to the CS while they receive the saline infusion. Control group II will also undergo
an fMRI scan and will be given saline infusion followed by ethanol infusion during their last
15 minutes in the scanner to control for the non-specific effects of repeated infusions &
scans on BOLD response to ethanol. If we are able to produce a CR in brain regions associated
with motivation, it may be possible to use this CR as an experimental model for human alcohol
craving.
question:
Which brain regions are activated in humans by the rewarding properties of ethanol
administration?
Is it possible to demonstrate a conditioned response to a stimulus paired with rising blood
alcohol concentrations (BAC) in humans and can this response be observed in the brain using
functional magnetic resonance images (fMRI) techniques?
Part 1. In order to determine which brain regions are activated by the rewarding properties
of ethanol administration, we propose to use Blood Oxygenation Level Dependent (BOLD) fMRI
techniques to test the hypothesis that during the time of rising and peak BAC, mesolimbic,
mesocortical, and nigrostriatal dopamine (DA) terminal areas of the brain will show
significant increases in cerebral blood flow. Healthy, non-alcoholic subjects will be given
intravenous (IV) ethanol or placebo infusions on separate days. The infusions will have three
phases. On each day, during the first phase a saline infusion will be used to measure basal
brain blood flow. The second phase will be an ethanol infusion delivered at rates calculated
to produce a BAC of 0.08 plus or minus 0.005 g/dl at 10 minutes. The rate of the infusion for
the next 10 minutes (third phase) will be calculated to maintain BAC at the target level of
0.08 plus or minus 0.005 g/dl for the duration of the infusion. On the placebo day, subjects
will receive a saline infusion at the same set of rates for phases two and three as used
during their ethanol infusion. Continuous multi-slice fMRI data will be collected during each
infusion.
Part 2. In order to investigate conditioned response to ethanol, three groups of healthy,
non-alcoholic subjects will be given a series of IV infusions on separate days. The
experimental group will receive ethanol infusion paired with a conditioned stimulus (CS)
which will be presented while the BAC is rising. One control group (I) of healthy,
non-alcoholic subjects will also be given a series of intravenous ethanol infusions on
separate days, but these infusions will not be paired with a CS. The other control group (II)
will be given only saline infusions during the CS presentation. After three training
sessions, all three groups will undergo an fMRI scan during which the CS will be paired with
saline infusion. This will allow the response to the CS alone to be observed. After 10
minutes of CS presentation, the ethanol infusion will begin and continue for another 15
minutes. Conditioned response (CR) will be demonstrated if the experimental group shows
greater increase in BOLD signal than the control groups in motivation areas such as
mesolimbic, mesocortical, and nigrostriatal dopamine (DA) terminal areas of the brain in
response to the CS while they receive the saline infusion. Control group II will also undergo
an fMRI scan and will be given saline infusion followed by ethanol infusion during their last
15 minutes in the scanner to control for the non-specific effects of repeated infusions &
scans on BOLD response to ethanol. If we are able to produce a CR in brain regions associated
with motivation, it may be possible to use this CR as an experimental model for human alcohol
craving.
This study is designed to answer four questions:
1. Which brain regions are activated in humans by the rewarding properties of ethanol
administration?
2. How does ethanol administration affect the brain response to visual cues known to evoke
positive or negative emotion?
3. Do individuals who regularly drink in ethanol in large amounts (heavy drinkers) differ
from individuals who do not regularly drink large amounts of ethanol (social drinkers)
in how ethanol affects brain function?
4. Does ethanol administration affect the brain regions activated in a risk-taking task in
social drinkers and heavy drinkers?
In order to determine which brain regions are activated by the rewarding properties of
ethanol administration, we propose to use Blood Oxygenation Level Dependent (BOLD) fMRI
techniques to test the hypothesis that during the time of rising and peak BAC, mesolimbic,
mesocortical, and nigrostriatal dopamine (DA) terminal areas of the brain will show
significant increases in cerebral blood flow. Healthy, subjects who are not seeking treatment
for an alcohol use disorder will be given intravenous (IV) ethanol or placebo infusions on
separate days. An ethanol infusion will delivered at rates calculated to produce a BAC of
0.08 plus or minus. An ethanol infusion will delivered at rates calculated to produce a BAC
of 0.08 plus or minus 0.005 g/dl at 15 minutes. Then the rate of the infusion will be
adjusted so that for the next 30 minutes (second phase) BAC will be maintained at the target
level of 0.08 0.005 g/dl. On the placebo day, subjects will receive a saline infusion at the
same set of rates as used during their ethanol infusion. Continuous multi-slice fMRI data
will be collected during each infusion. During each infusion, BOLD response to visual stimuli
designed to evoke emotion will also be examined. In addition, we will compare the BOLD
response of healthy social drinkers to that of healthy heavy drinkers. We will also compare
the BOLD response elicited by risk-taking during the ethanol infusion to that during the
placebo infusion in both social and heavy drinkers.
1. Which brain regions are activated in humans by the rewarding properties of ethanol
administration?
2. How does ethanol administration affect the brain response to visual cues known to evoke
positive or negative emotion?
3. Do individuals who regularly drink in ethanol in large amounts (heavy drinkers) differ
from individuals who do not regularly drink large amounts of ethanol (social drinkers)
in how ethanol affects brain function?
4. Does ethanol administration affect the brain regions activated in a risk-taking task in
social drinkers and heavy drinkers?
In order to determine which brain regions are activated by the rewarding properties of
ethanol administration, we propose to use Blood Oxygenation Level Dependent (BOLD) fMRI
techniques to test the hypothesis that during the time of rising and peak BAC, mesolimbic,
mesocortical, and nigrostriatal dopamine (DA) terminal areas of the brain will show
significant increases in cerebral blood flow. Healthy, subjects who are not seeking treatment
for an alcohol use disorder will be given intravenous (IV) ethanol or placebo infusions on
separate days. An ethanol infusion will delivered at rates calculated to produce a BAC of
0.08 plus or minus. An ethanol infusion will delivered at rates calculated to produce a BAC
of 0.08 plus or minus 0.005 g/dl at 15 minutes. Then the rate of the infusion will be
adjusted so that for the next 30 minutes (second phase) BAC will be maintained at the target
level of 0.08 0.005 g/dl. On the placebo day, subjects will receive a saline infusion at the
same set of rates as used during their ethanol infusion. Continuous multi-slice fMRI data
will be collected during each infusion. During each infusion, BOLD response to visual stimuli
designed to evoke emotion will also be examined. In addition, we will compare the BOLD
response of healthy social drinkers to that of healthy heavy drinkers. We will also compare
the BOLD response elicited by risk-taking during the ethanol infusion to that during the
placebo infusion in both social and heavy drinkers.
- INCLUSION CRITERIA LIGHT DRINKERS:
1. in good health.
2. between 21 and 45 years of age.
3. Currently consuming between 1 and 14 drinks per week.
EXCLUSION CRITERIA LIGHT DRINKERS:
1. have an abnormal physical exam and/or have laboratory values outside of normal ranges;
2. have fulfilled DSM-IV criteria for ethanol or other substance dependency (excluding
nicotine) at any time;
3. have fulfilled DSM-IV criteria for a current or past major psychiatric disorder
(DSM-IV Axis I) or who have ever had a head injury requiring hospitalization.
4. are over or under 20% of ideal body weight;
5. have taken any prescribed, non-prescribed, or over-the-counter medications or drugs
within 14 days prior to the study days (excluding oral contraceptive agents);
6. are pregnant;
7. report to have a "facial flushing" response to the consumption of ethanol;
8. have never consumed at least two standard drinks of ethanol within one hour.
9. have ferromagnetic objects in their bodies, which might be adversely affected by MRI
(e.g., surgical clips, metal fragments in or near brain, eye or blood vessels, cardiac
or neurological pacemaker, cochlear or eye implant). Any doubt about presence of these
objects will result in exclusion from this study.
10. Additionally, subjects will be asked to abstain from ethanol for at least 2 days prior
to the studies.
11. Regular tobacco users will be excluded from the study in order to avoid nicotine
withdrawal symptoms. Occasional (not daily) use of tobacco products is acceptable.
INCLUSION CRITERIA HEAVY DRINKERS:
1. in good health.
2. between 21 and 45 years of age.
3. currently consuming between 20 and 40 drinks per week.
4. not regularly abstinent for more than 3 days per week, but have abstained from alcohol
for 3 consecutive days without experiencing withdrawal symptoms.
5. able to provide a plausible history that they can abstain from alcohol without
significant withdrawal symptoms when coming to the clinic. In addition, each
participant will be asked to quantify their worst withdrawal symptoms using the
Clinical Institute Withdrawal Assessment (CIWA) Instrument. Participants who score 8
or above will not be enrolled in the protocol.
6. not seeking treatment for their alcohol consumption.
EXCLUSION CRITERIA HEAVY DRINKERS:
1. have an abnormal physical exam and/or have laboratory values outside of normal ranges;
2. have fulfilled DSM-IV criteria for any substance dependency (excluding alcohol or
nicotine) at any time;
3. have fulfilled DSM-IV criteria for a current or past major psychiatric disorder or who
have ever had a head injury requiring hospitalization.
4. are over or under 20% of ideal body weight;
5. have taken any prescribed, non-prescribed, or over-the-counter medications or drugs
within 14 days prior to the study days (excluding oral contraceptive agents);
6. are pregnant;
7. report to have a "facial flushing" response to the consumption of ethanol;
8. have never consumed at least two standard drinks of ethanol within one hour.
9. have ferromagnetic objects in their bodies, which might be adversely affected by MRI
(e.g., surgical clips, metal fragments in or near brain, eye or blood vessels, cardiac
or neurological pacemaker, cochlear or eye implant). Any doubt about presence of these
objects will result in exclusion from this study.
10. Additionally, subjects will be asked to abstain from ethanol for at least 2 days prior
to the studies.
11. Regular tobacco users will be excluded from the study in order to avoid nicotine
withdrawal symptoms. Occasional (not daily) use of tobacco products is acceptable.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
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