Abstract:
Analgesic (for both neuropathic and nociceptive pain) and anticonvulsant action of 7-bromo-5-(o-chlorophenyl)-3-
propoxy-1,2-dihydro-3H-1,4-benzodiazepin-2-one (propoxazepam) make it perspective for further studying. Objectives: Propoxazepam
was evaluated for sedative-hypnotic-like activity in mice and involved mechanisms in a battery of tests: acute oral toxicity, motor
coordination and muscle relaxation studies. Materials and Methods: Acute toxicity (rats) and thiopental-induced sleeping (mice) were
determined as motor coordination and muscle relaxation. Results: As relatively nontoxic substance (LD50>5000 mg/kg) propoxazepam
belong to fifth category according to GHS toxicity classification. At high doses (700, 1100 and 1300 mg/kg, i.p.) a delay in the righting
reflex was observed but not a total loss. The results indicated that substance induces hypnotic effects. Because propoxazepam produces
any effect on rotarod test, seems that its effects on sleeping time and sleep latency are mediated by affecting motor movement.
Conclusion: Based on previous results and present data, it should be presumed that GABAergic mechanisms may be involved in the
potentiating effect of propoxazepam on thiopental-induced sleeping time and sleep latency in mice. Propoxazepam potentiates sleep
induced by hypnotics like thiopental, but can not induce hypnosis by itself.
