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Last Updated: 3 years ago

Possible Interaction: Ethanol and Buspirone

supplement:

Ethanol

Research Papers that Mention the Interaction

OBJECTIVE Previous research has suggested that both lithium and buspirone could lessen alcoholics' desire to drink as well as reduce the actual amounts of alcohol consumed.
Alcoholism, clinical and experimental research  •  2000  |  View Paper
In animals, buspirone has been shown to alter drinking preference from alcohol to water.
Psychopathology  •  1989  |  View Paper
The 5-HT1A receptor agonist buspirone is an anxiolytic which has been shown to diminish the desire to consume alcohol in anxious alcoholic patients.
The British journal of psychiatry. Supplement  •  1991  |  View Paper
Buspirone offsets some of the impairment due to alcohol when the agents are combined.
Pharmacotherapy  •  1984  |  View Paper
Finally, we evaluated buspirone , an approved drug for anxiety disorders endowed with D3R antagonist activity (confirmed by molecular modeling analysis), that resulted effective in inhibiting ethanol intake.
Neuropsychopharmacology  •  2014  |  View Paper
Buspirone , a 5-HT1A agonist, has been shown to decrease the intake of ethanol when given as a single dose to rats with a psychological dependence induced according to our rat model of alcoholism.
On the first day, the buspirone injection decreased ethanol intake from the pretreatment value (1.94+/-0.18 g/kg/day), down to 1.36+/-0.18 g/kg (p < 0.01, n = 12).
Thus, an acute dose of buspirone can decrease voluntary ethanol intake in psychologically dependent rats, but long-lasting changes in the effect of buspirone seem to develop during a 3-week treatment period.
Alcoholism, clinical and experimental research  •  1999  |  View Paper
d-Fenfluramine, fluoxetine, buspirone , TFMPP, and DOI all produced a reduction in ethanol ingestion and maintained behaviour at doses that failed to reduce LMA.
Alcohol  •  1998  |  View Paper
In this situation, with a longer exposure to ethanol , a dose of 20 mg/kg of buspirone in week 90 reduced ethanol intake by approximately 40%, when compared with controls.
Alcohol and alcoholism  •  1996  |  View Paper
Ethanol intake is significantly suppressed by zimelidine, bromocriptine, buspirone , and lithium carbonate, pharmacological agents that have been shown to be beneficial in controlling ethanol intake in alcohol-dependent humans.
Proceedings of the National Academy of Sciences of the United States of America  •  1993  |  View Paper
The anxiogenic behaviour observed 12 h after ethanol withdrawal was inhibited by the 5-HT1A partial agonist, buspirone (200 micrograms/kg s.c.),
Alcohol and alcoholism (Oxford, Oxfordshire). Supplement  •  1993  |  View Paper
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