al-Tajir G, Starr M S
Department of Pharmacology, School of Pharmacy, London University, U.K.
Eur J Pharmacol. 1990 Dec 4;191(3):329-36. doi: 10.1016/0014-2999(90)94165-t.
This study investigates the role of forebrain D1 receptors in the motor expression of seizures induced by pilocarpine. Conscious rats receiving bilateral intracaudate injections of saline, just failed to convulse to 200 mg/kg pilocarpine, but responded vigorously to 600 mg/kg of the cholinomimetic. LY 171555 significantly protected rats against 600 mg/kg pilocarpine, when delivered into the anterior striatum, as also did SCH 23390, from all rostrocaudal levels of the striatum. Intrastriatal SKF 38393 or CY 208-243 neither facilitated nor ameliorated pilocarpine-induced convulsions. SCH 23390 was also anticonvulsant from the nucleus accumbens, while intra-accumbens CY 208-243 was without effect. It is concluded that SCH 23390 affords protection against pilocarpine-induced limbic motor seizures by blocking the effects of endogenous dopamine released tonically onto D1 receptors in the corpus striatum and nucleus accumbens. The inability of additional D1 receptor stimulation to intensify such seizures, could indicate that forebrain D1 receptors are already maximally stimulated by the endogenous transmitter.
本研究调查了前脑D1受体在毛果芸香碱诱导的癫痫发作运动表现中的作用。清醒大鼠双侧尾状核内注射生理盐水后,对200mg/kg毛果芸香碱未能惊厥,但对600mg/kg拟胆碱药有强烈反应。当注入纹状体前部时,LY 171555和SCH 23390(从纹状体所有头尾水平注入)均能显著保护大鼠免受600mg/kg毛果芸香碱的影响。纹状体内注射SKF 38393或CY 208 - 243既不促进也不改善毛果芸香碱诱导的惊厥。SCH 23390从伏隔核注入时也具有抗惊厥作用,而伏隔核内注射CY 208 - 243则无效。结论是,SCH 23390通过阻断内源性多巴胺持续释放到纹状体和伏隔核中D1受体上的作用,对毛果芸香碱诱导的边缘性运动性癫痫发作起到保护作用。额外的D1受体刺激无法增强此类癫痫发作,这可能表明前脑D1受体已被内源性递质最大程度地激活。