Summary
Low doses (300μ/kg-1.0 mg/kg) of the novelβ-carboline, ZK 91 296, a putative agonist at the benzodiazepine receptor, produced a significant increase in the rate of variable-interval self-stimulation responding, similar to that found with typical benzodiazepines. This effect was blocked by simultaneous administration of the specific benzodiazepine-receptor antagonists Ro 15-1788 (2.0 mg/kg), and ZK 93 426 (10 mg/kg). Neither antagonist, ZK 93 426 (100μg/kg-10 mg/kg) or Ro 15-1788 (2.0 mg/kg), had any effect on self-stimulation when given alone. Unlike all benzodiazepine-receptor agonists previously tested, higher doses of ZK 91 296 did not depress self-stimulation response rates, even at a dose-level 100 times greater than the maximally stimulant dose. It is uncertain why ZK 91 296 lacks depressant effects: available evidence does not conclusively favour any single current explanation, but is consistent with it acting as a “partial” agonist.
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Herberg, L.J., Montgomery, A.M.J., File, S.E. et al. Effect on hypothalamic self-stimulation of the novelβ-carbolines ZK 93 426 (a benzodiazepine receptor antagonist) and ZK 91296 (a putative partial agonist). J. Neural Transmission 66, 75–84 (1986). https://doi.org/10.1007/BF01260903
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DOI: https://doi.org/10.1007/BF01260903