Zirvi K A, Fakouhi T
Arzneimittelforschung. 1977;27(6):1194-8.
The neuropharmacology of phenylurea was studied. The compound is a potent sedative hypnotic agent with a fairly good margin of safety. It produced significant motor incoordination and behavioral changes in sub-sedative doses, thus suggesting that it acts on the areas of the brain which control motor coordination (neurological deficit) and spontaneous motor movements (awareness of environment). The activity pattern of phenylurea as measured on the rotarod treadmill was identical with that of an ataractic drug, meprobamate, and different from that of the sedative drug, 2-ethylcrotonylurea (ectylurea). It exhibited significant meprobamate-like antistrychnine (myorelaxant) activity, and at high doses only, anticonvulsant activity (pentetrazole antagonism). Phenylurea also protected mice against tremorine-induced tremors. A sub-sedative dose of phenylurea significantly prolonged pentobarbital sleeping time.
对苯基脲的神经药理学进行了研究。该化合物是一种强效镇静催眠剂,具有相当好的安全范围。在亚镇静剂量下,它会产生明显的运动不协调和行为变化,因此表明它作用于控制运动协调(神经功能缺损)和自发运动(对环境的意识)的脑区。在旋转棒跑步机上测量的苯基脲的活性模式与镇静安定药甲丙氨酯相同,与镇静药2-乙基巴豆酰脲(乙基脲)不同。它表现出显著的类似甲丙氨酯的抗士的宁(肌松)活性,且仅在高剂量时具有抗惊厥活性(戊四氮拮抗作用)。苯基脲还能保护小鼠免受震颤素诱发的震颤。亚镇静剂量的苯基脲能显著延长戊巴比妥睡眠时间。