Alcoholism Clinical Trial
Official title:
The Effects of Levetiracetam on Alcohol Dependent Subjects
This study will attempt to examine whether Levetiracetam (Keppra (TM)) can help people with alcohol dependence cut down on their alcohol consumption. In addition, the investigation will assess the effectiveness of Keppra on reducing withdrawal symptoms post alcohol cessation. Matched group of historical controls of alcohol dependent patients receiving placebo will be used for comparison.Based on the mechanism of action of Keppra we hypothesize that it may be effective in promoting abstinence and reducing drinking behavior in alcohol dependent patients.
Alcoholism is a chronic disease with numerous psychological, social and medical
consequences. Alcohol use disorders are one of the most prevalent psychiatric disorders in
general population in the US. Alcoholism not only disrupts an individual's life, health and
ability to function in the society, has tremendous impact on families and communities, but
also is associated with enormous economic cost for society. The medical and social impact of
alcoholism can be reduced via effective treatments. Although medical, psychological and
social approaches have demonstrated some efficacy, no specific method has consistently shown
superiority. Similarly, currently available pharmacological treatments for alcohol use
disorders are associated with moderate efficacy, indicating that further efforts are
required to develop novel interventions.
The rewarding effects of alcohol are at least partially mediated via dopamine pathways that
originate in the ventral tegmental area and project to the nucleus accumbens. Alcohol
through its effects on GABA receptor activity decreases the inhibitory effect of GABA on the
dopaminergic neurons in ventral tegmental area and therefore facilitates dopamine
neurotransmission. Medications that modulate excitatory neurotransmission in the brain
(glutamate) and facilitate inhibitory effects of GABA have been shown to be clinically
effective in treatment of alcoholism.
Keppra is a novel antiepileptic medication currently approved for treatment of partial onset
seizures as an adjunctive agent. It has a unique mechanism of action in that it reduces
negative allosteric effects of Zn++ and Beta- carboline in two main inhibitory receptors in
the CNS- the GABA A and glycine receptors. These modulators inhibit the influx of chloride
though both of these receptor complexes and are therefore considered excitatory mediators.
Keppra prevents the negative modulation and promotes chloride flux, thereby, inhibiting
neurotransmission.
Limited laboratory work with levetiracetam (Keppra) has shown that the medication can
reverse the anxiogenic effect of benzodiazepine withdrawal in mice (Y. Lamberty et al.,
2002). Furthermore, Keppra was investigated for its potential to prevent alcohol withdrawal
symptoms in mice. In this study levetiracetam dose-dependently prevented spontaneous tremors
and handling induced convulsions in alcohol dependent mice. (Y. Lamberty et al., 2002).
Based on the mechanism of action of Keppra we hypothesize that it may be effective in
promoting abstinence and reducing drinking behavior in alcohol dependent patients.
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