Hepatic encephalopathy is ameliorated by drugs acting on the central GABAA-
benzodiazepine receptor complex. To investigate whether these effects are specific for
hepatic encephalopathy or just reflect a nonspecific arousal reaction, various
benzodiazepine antagonists like
flumazenil or with inverse agonistic properties (
Ro 15-4513,
Ro 15-3505) were studied in uremic
encephalopathy in rats after bilateral ureteral
ligation (n = 20) and compared with
hepatic encephalopathy caused by
thioacetamide-induced
acute liver failure (n = 33). As soon as the animals developed clear signs of
metabolic encephalopathy, their motor activity was recorded in an animal activity meter for 10 min. Furthermore, a composite score was calculated by grading various behavioral signs from 0 = absent to 3 = apparently normal. Rats were then injected with coded preparations of
Ro 15-4513 (0.5, 2.5 and 5 mg/kg body wt intraperitoneally),
flumazenil (2.5, 10, 25 and 40 mg/kg),
Ro 15-3505 (10 mg/kg) or vehicle, and the measurements were repeated. The code was broken after the completion of the study. Pretreatment motor activity was decreased both in hepatic and uremic
encephalopathy (20.7 +/- 6.4 [S.E.M.] and 41.3 +/- 37.1 movements/10 min). In
hepatic encephalopathy motor activity and the composite score were improved both by 5 mg/kg
Ro 15-4513 (by 293%, p less than 0.05) and by 10 mg/kg
Ro 15-3505 (by 509%, p greater than 0.01), whereas vehicle and
flumazenil had no effects. In uremic
encephalopathy neither
drug was effective in improving the neurobehavioral status.(ABSTRACT TRUNCATED AT 250 WORDS)