Kulkarni S K
Arch Int Pharmacodyn Ther. 1981 Jul;252(1):124-32.
Pretreatment of rats and mice with clonidine (0.5-5 mg/kg, intraperitoneally) protected the animals against tonic convulsions induced by picrotoxin, strychnine and maximal electroshock, respectively. The time of onset of convulsions as well as mortality due to picrotoxin and strychnine were delayed in the clonidine pretreated groups as compared to controls. Clonidine (1 mg/kg) blocked the extensor phase of the electroshock convulsion. In reserpinized animals the severity of electroshock-induced seizures was reduced by clonidine pretreatment. Clonidine also caused an increase in the food consumption behaviour in mice subjected to novel situation and food. Its effects were comparable to diazepam, an antianxiety agent. In another experiment, clonidine (0.5-5 mg/kg) counteracted the perphenazine-induced catatonia in rats. It is possible that the observed anticatatonic effect of clonidine may be due to its presynaptic activity, but the actual mechanism of this action is not yet understood.
用可乐定(0.5 - 5毫克/千克,腹腔注射)对大鼠和小鼠进行预处理,可分别保护动物免受印防己毒素、士的宁和最大电休克诱导的强直性惊厥。与对照组相比,可乐定预处理组中由印防己毒素和士的宁引起的惊厥发作时间以及死亡率均延迟。可乐定(1毫克/千克)阻断了电休克惊厥的伸肌期。在利血平化的动物中,可乐定预处理可降低电休克诱导的癫痫发作的严重程度。可乐定还使处于新环境和面对食物的小鼠的食物消耗行为增加。其效果与抗焦虑药地西泮相当。在另一项实验中,可乐定(0.5 - 5毫克/千克)抵消了大鼠中奋乃静诱导的紧张症。可乐定观察到的抗紧张症作用可能归因于其突触前活性,但其实际作用机制尚不清楚。