Ii has been suggested that decreased central GABAergic activity may pl
ay a role in the pathogenesis of alcoholism. Sodium valproate is a com
mercially available anticonvulsant that increases central GABAergic ac
tivity. In this pilot study 13 adult male alcoholics received one mont
h of oral, low dose sodium valproate (15 mg/kg/d) followed by one mont
h of placebo followed by one month of sodium valproate at the standard
anticonvulsant dosage (45 mg/kg/d). The principle objective of the st
udy was to determine if sodium valproate is well tolerated and free of
adverse effects in this high risk group. Anxiety levels and the desir
e to drink alcohol were also monitored throughout the study period. Th
e results of the study revealed that low dose sodium valproate therapy
is well tolerated and free of toxicity. While anxiety levels tended t
o fall or remained unchanged in the seven patients who completed four
weeks of low dose treatment, there was no consistent change in their d
esire to drink values. Too few patients completed the trial to ascerta
in the safety or efficacy of standard dose sodium valproate. These fin
dings suggest that controlled clinical trials of sodium valproate are
feasible in adult male alcoholics.