Stripling J S, Hendricks C
Pharmacol Biochem Behav. 1981 Nov;15(5):793-8. doi: 10.1016/0091-3057(81)90024-1.
The effect of drug-induced convulsions on kindling was studied in male Long-Evans rats. In Experiment 1 rats experienced a single convulsion induced by the intravenous infusion of cocaine, lidocaine, or pentylenetetrazol (PTZ), or received a control infusion of saline. Beginning eight days later all animals were kindled by daily stimulation of the olfactory bulb. Animals which had been convulsed by cocaine or lidocaine kindled significantly faster than either saline controls or PTZ-convulsed animals, which did not differ significantly. Experiment 2 was conducted to determine if an effect of PTZ on kindling could be obtained with repeated convulsions. Rats experienced three convulsions induced by cocaine or PTZ at 72 hr intervals, or control infusions of saline. Kindling began on the eighth day after the last infusion. Cocaine-convulsed animals again kindled significantly faster than saline or PTZ-convulsed animals, which did not differ significantly. The cocaine animals also had significantly longer afterdischarges than the saline group at the end of kindling and when stimulated again 21 days after kindling was completed. These results suggest that the facilitating effect of cocaine-induced convulsions is not a general property of all convulsants but is a more specific effect which is apparently shared by other local anesthetics.
在雄性长 Evans 大鼠中研究了药物诱发惊厥对点燃效应的影响。在实验 1 中,大鼠通过静脉注射可卡因、利多卡因或戊四氮(PTZ)诱发单次惊厥,或接受生理盐水对照注射。从八天后开始,所有动物每天通过刺激嗅球进行点燃。因可卡因或利多卡因诱发惊厥的动物点燃速度明显快于生理盐水对照动物或 PTZ 诱发惊厥的动物,后两者之间无显著差异。进行实验 2 以确定重复惊厥是否能产生 PTZ 对点燃效应的影响。大鼠每隔 72 小时通过可卡因或 PTZ 诱发三次惊厥,或接受生理盐水对照注射。在最后一次注射后的第八天开始点燃。可卡因诱发惊厥的动物再次比生理盐水或 PTZ 诱发惊厥的动物点燃速度明显快,后两者之间无显著差异。在点燃结束时以及点燃完成 21 天后再次刺激时,可卡因处理的动物的后放电时间也明显长于生理盐水组。这些结果表明,可卡因诱发惊厥的促进作用并非所有惊厥剂的普遍特性,而是一种更具特异性的效应,其他局部麻醉剂显然也具有这种效应。