Amitifadine, a triple monoamine uptake inhibitor, reduces binge drinking and negative affect in an animal model of co-occurring alcoholism and depression symptomatology |
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Authors: | Kaitlin T Warnock Andrew R S T Yang Heon S Yi Harry L June Timothy Kelly Anthony S Basile Phil Skolnick Harry L June |
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Affiliation: | a Neuropsychopharmacology Laboratory, Department of Psychiatry and Behavioral Sciences, Howard University College of Medicine, Washington, DC 20060, USAb DOV Pharmaceutical, Inc., Somerset, NJ 08873, USAc Department of Pharmacology, Howard University College of Medicine, Washington, DC 20060, USA |
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Abstract: | The co-occurrence of alcoholism and depression is highly prevalent and difficult to treat. In an animal model of binge drinking that exhibits abstinence-induced behaviors reminiscent of negative affective states, the triple monoamine uptake inhibitor, amitifadine, produced a selective, dose dependent attenuation of binge drinking. Amitifadine also reversed abstinence-induced increases in the intracranial self-stimulation threshold, a model of anhedonia, and immobility in the forced swim test, reflecting behavioral despair. In view of the safety profile of amitifadine in humans, including low risk for weight gain, lack of sexual side effects, and low potential for abuse, we hypothesize that amitifadine will be effective in treating co-occurring alcoholism and depression. |
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Keywords: | Alcoholism Depression Triple uptake inhibitor Anhedonia Negative affective states Behavioral despair |
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