Wada J A, Mizoguchi T, Osawa T
Neurology. 1978 Oct;28(10):1026-36. doi: 10.1212/wnl.28.10.1026.
Amygdaloid kindling in rhesus monkeys resulted in development of secondarily generalized convulsive seizures in an average of 196 days. Prior pharmacologic (bemegride) kindling accelerated this seizure development in one animal. None of the animals reached the stage 5 primary generalized seizure of baboons (Papio papio), even after 400 daily amygdaloid stimulations. Seizure stage instability, with frequent regression to an earlier stage, and the difficulty of establishing a generalized seizure triggering threshold in most of the rhesus monkeys, contrasts with our experiences in Papio papio. Thus, differences in the speed of kindling and in the quality of kindled convulsion between rhesus monkeys and epileptic baboons probably reflect the presence or absence of an epileptogenic predisposition in these two species. The difficulty of developing convulsive seizure in rhesus monkeys suggests that this species is particularly suited for the study of partial complex seizure. These studies indicate that the abrupt onset of human epilepsy with a fully developed convulsive seizure must represent and overwhelming central pathophysiologic event resulting from an endogenous, exogenous or a combined insult interacting with a genetically predisposed seizure susceptibility.
恒河猴杏仁核点燃平均在196天后会导致继发性全身性惊厥发作。先前的药理学(美解眠)点燃在一只动物中加速了这种发作的发展。即使经过400次每日杏仁核刺激,没有一只动物达到狒狒(巴氏狒狒)的5期原发性全身性发作阶段。发作阶段不稳定,频繁退回到早期阶段,并且在大多数恒河猴中难以建立全身性发作触发阈值,这与我们在巴氏狒狒中的经验形成对比。因此,恒河猴和癫痫狒狒在点燃速度和点燃惊厥质量上的差异可能反映了这两个物种中是否存在致痫易感性。恒河猴中难以发生惊厥性发作表明该物种特别适合用于部分复杂性发作的研究。这些研究表明,人类癫痫伴有完全发展的惊厥性发作的突然发作必定代表着由内源性、外源性或联合损伤与遗传易感性癫痫易感性相互作用而导致的压倒性中枢病理生理事件。