Dalton J C, Roberts D C, McIntyre D C
Psychopharmacology (Berl). 1985;85(3):319-22. doi: 10.1007/BF00428195.
Electrically induced focal cortical seizures were examined in 6-hydroxydopamine (6-OHDA) pretreated or control rats in the presence of 0, 1, 2.5, 5, and 10 micrograms/kg clonidine. In baseline determinations, rats pretreated with 6-OHDA showed lower seizure thresholds and longer behavioral and electrographic seizure than controls. Consistent with other reports, the lowest dose of clonidine (1 microgram/kg) inhibited seizures in control animals; 6-OHDA potentiated the anticonvulsant effect of the lowest dose of clonidine but exacerbated seizure in the presence of the highest dose of clonidine (10 micrograms/kg). Since others have reported proconvulsant effects of clonidine at much higher doses (100 or 1,000 micrograms/kg) using control animals, the depletion of forebrain norepinephrine with 6-OHDA therefore appears to produce a supersensitivity both to the proconvulsant and to the anticonvulsant effect of clonidine. These data suggest that the receptors that mediate the proconvulsant (possibly alpha 1 adrenoceptors) and the anticonvulsant (possibly alpha 2 adrenoceptors) effects are located postsynaptically.
在0、1、2.5、5和10微克/千克可乐定存在的情况下,对6-羟基多巴胺(6-OHDA)预处理的大鼠或对照大鼠进行电诱导局灶性皮质癫痫发作研究。在基线测定中,用6-OHDA预处理的大鼠比对照大鼠表现出更低的癫痫发作阈值以及更长的行为和脑电图癫痫发作时间。与其他报告一致,最低剂量的可乐定(1微克/千克)可抑制对照动物的癫痫发作;6-OHDA增强了最低剂量可乐定的抗惊厥作用,但在最高剂量可乐定(10微克/千克)存在时加剧了癫痫发作。由于其他人使用对照动物报告了更高剂量(100或1000微克/千克)可乐定的促惊厥作用,因此用6-OHDA耗竭前脑去甲肾上腺素似乎会导致对可乐定的促惊厥和抗惊厥作用均产生超敏反应。这些数据表明,介导促惊厥作用(可能是α1肾上腺素能受体)和抗惊厥作用(可能是α2肾上腺素能受体)的受体位于突触后。