Post R M, Squillace K M, Pert A, Sass W
Psychopharmacology (Berl). 1981;72(2):189-96. doi: 10.1007/BF00431655.
Interactions of amygdala kindling and drug effects were explored in two experiments. Pretreatment with cocaine (40 mg/kg, IP) for 10 days did not significantly affect the rate of amygdala kindling compared to saline or non-kindled controls. In contrast, daily amygdala kindling with 200 microA for 0.5 s for 20 days substantially altered subsequent behavioral responses in a long-lasting fashion. Animals showed decreased spontaneous vertical rearing activity, as well as decreased cocaine-induced vertical activity. In contrast, they were more reactive to the direct dopamine receptor agonist apomorphine. Eighteen days following completion of amygdala kindling, kindled animals were more sensitive to lidocaine-induced convulsions; 88% of kindled animals, but only 24% of the implanted sham-stimulated controls, had seizures. These data suggest that amygdala kindling may produce long-lasting changes in selected spontaneous and drug-induced behaviors, as well as convulsive thresholds. Possible physiological and neurological changes underlying this altered responsivity are discussed.
在两项实验中探究了杏仁核点燃与药物效应的相互作用。与生理盐水或未点燃的对照组相比,用可卡因(40毫克/千克,腹腔注射)预处理10天对杏仁核点燃速率没有显著影响。相反,每天用200微安刺激杏仁核0.5秒,持续20天,会以一种持久的方式显著改变随后的行为反应。动物的自发垂直活动减少,可卡因诱导的垂直活动也减少。相比之下,它们对直接多巴胺受体激动剂阿扑吗啡的反应更强。杏仁核点燃完成18天后,点燃的动物对利多卡因诱导的惊厥更敏感;88%的点燃动物出现癫痫发作,而植入假刺激的对照组只有24%出现癫痫发作。这些数据表明,杏仁核点燃可能会在特定的自发行为、药物诱导行为以及惊厥阈值方面产生持久变化。讨论了这种反应性改变背后可能的生理和神经变化。