Evidence for the presence of a benzodiazepine receptor binding substance in cerebrospinal fluid of a rabbit model of hepatic encephalopathy |
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Authors: | K. D. Müllen J. V. Martin W. B. Mendelson K. Kaminsky-Russ E. A. Jones |
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Affiliation: | (1) Department of Medicine, Division of Gastroenterology, Cleveland Metropolitan General Hospital, Case Western Reserve University, 44109 Cleveland, Ohio;(2) Department of Psychiatry and Behavioral Science, State University of New York, 11794 Stony Brook, New York;(3) Liver Diseases Section, NIDDK, NIH, 20892 Bethesda, Maryland |
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Abstract: | Based on the reversal of hepatic encephalopathy in animal models with administration of specific benzodiazepine receptor antagonists, it has been postulated that this syndrome may be mediated by an endogenous benzodiazepine-like compound. In this study using a radioreceptor assay, evidence for the existence of this substance has been demonstrated in cerebrospinal fluid but not sera of rabbits with hepatic encephalopathy due to galactosamine induced hepature failure. Cerebrospinal fluid from rabbits with hepatic encephalopathy caused 36.1 ± 5.03% displacement of3H-Ro 15-1788 specific binding to cortical benzodiazepine receptors, compared to 11.7 ± 0.76% in control animals (P < 0.01). The benzodiazepine receptor binding activity has been shown to behave as a competitive inhibitor of radiolabeled benzodiazepine receptor binding. The finding of endogenous benzodiazepine binding activity affords a potential explanation for the amelioration of hepatic encephalopathy in this model with the administration of benzodiazepine receptor antagonists. |
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Keywords: | hepatic encephalopathy endogenous benzodiazepine activity fulminant hepatic failure |
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