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Behavioral effects of non‐opioid antitussive anticonvulsants
Author(s) -
Witkin Jeffrey M.,
Tortella Frank C.
Publication year - 1989
Publication title -
drug development research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.582
H-Index - 60
eISSN - 1098-2299
pISSN - 0272-4391
DOI - 10.1002/ddr.430180107
Subject(s) - anticonvulsant , dextromethorphan , pharmacology , diazepam , anxiolytic , opioid , benzodiazepine , naltrexone , chemistry , epilepsy , medicine , psychology , receptor , neuroscience
Abstract Many of the currently used anticonvulsants possess a host of undesirable pharmacological properties. Several non‐opioid antitussives bind to high‐affinity [ 3 H]dextromethorphan sites in brain and have novel anticonvulsants activity. Because these compounds may be useful in the treatment of some epilepsies, either alone or as adjuncts. Behavioral effects of these as well as clinically used anticonvulsant drugs were studied under a standard preclinical test of sedative‐hypnotic/anxiolytic activity which generally yieds positive results with standard anticonvulsants. Lever‐press responses of male Sprague‐Dawley rats were maintained under a multiple schedule of food presentation in which responses in one component were suppressed by brief electric shock (punishment) whereas responses in an alternate component were not punished. The drug doses tested were the ED 50 and 2 X ED 50 for anticonvulsant activity against maximal electroshock‐induced convulsions. The non‐opioid antitussive anticonvulsants, carbetapentane, caramiphen, dextromethorphan, as well as diphenylhydantoin, did not increase punished responding, Nonpunished responding was unaffected by ED 50 does levels of these compounds. In contrast, diazepam increased punished responding to 800% of control levels and increased nonpunished responding at 1 mg/kg. Responding was typically decreased by the highest doses of all drugs studied except diphenylhydantion. Thus, the non‐opioid antitussive anticonvulsants were devoid of significant behavioral effects at the ED 50 does and did not possess the anxiolytic activity of benzodiazepine or barbiturate anticonvulsants.

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