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The spectra of pharmacological effects of ethanol and the benzodiazepine show a degree of overlap. Neurophysiological and neurochemical evidence indicates that both ethanol and benzodiazepines facilitate inhibitory neurotransmission mediated by GABA. Diazepam has been reported to inhibit both the tremor and mechanism of cerebellar cyclic GMP caused by harmaline by a neurotransmission in the cerebellum. Because of the similarities between ethanol and benzodiazepines, the effects of ethanol on harmaline-induced tremor and increase of cerebellar cyclic GMP were studied. Ethanol inhibited harmaline-induced tremor at doses as low as 0.1 g/kg. At this low dose, however, a dissociation between inhibition of harmaline tremor and inhibition of the harmaline-induced increase of cerebellar cyclic GMP was observed.
M S Rappaport, and
R T Gentry, and
D R Schneider, and
V P Dole
January 1993,
Psychopharmacology,
M S Rappaport, and
R T Gentry, and
D R Schneider, and
V P Dole
October 1986,
Life sciences,
M S Rappaport, and
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V P Dole
October 2021,
Heliyon,
M S Rappaport, and
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V P Dole
August 1973,
Experimental brain research,
M S Rappaport, and
R T Gentry, and
D R Schneider, and
V P Dole
January 1975,
Brain research,
M S Rappaport, and
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D R Schneider, and
V P Dole
January 1983,
Neurotoxicology,
M S Rappaport, and
R T Gentry, and
D R Schneider, and
V P Dole
June 2011,
Cerebellum (London, England),
M S Rappaport, and
R T Gentry, and
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V P Dole
October 2013,
Journal of neuroscience research,
M S Rappaport, and
R T Gentry, and
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V P Dole
October 1978,
Brain research,
M S Rappaport, and
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V P Dole
October 1987,
Life sciences,
