Corda M G, Orlandi M, Lecca D, Carboni G, Frau V, Giorgi O
Department of Experimental Biology, Chair of Pharmacology, University of Cagliari, Italy.
Pharmacol Biochem Behav. 1991 Oct;40(2):329-33. doi: 10.1016/0091-3057(91)90562-g.
The repeated administration of subconvulsant doses of pentylenetetrazol (PTZ) produced a progressive sensitization to the effects of this compound (i.e., chemical kindling) in the rat. A very similar time-course for PTZ-induced kindling was observed using two different treatment schedules: 1) one injection every day (30 mg/kg, IP), and 2) one injection (30 mg/kg, IP) every second day. When these treatment schedules were used for eight consecutive weeks, more than 80% of the rats displayed convulsions by the end of treatment. In contrast, only 20% of the rats were sensitized if PTZ was administered twice daily at the dose of 15 mg/kg, IP. The increased sensitivity to the convulsant effect of PTZ was still present one year after completion of the chronic treatment. Moreover, rats kindled with PTZ showed an enhanced susceptibility to convulsions induced by different inhibitors of central GABAergic function, such as the chloride channel blocker picrotoxin, the benzodiazepine receptor ligands FG 7142 and Ro 15-4513, and the inhibitor of GABA synthesis isoniazid. In contrast, the sensitivity to the convulsant action of the glycine receptor antagonist strychnine was unchanged by repeated PTZ administration. It is suggested that kindling produced by PTZ may be associated with a persistent reduction in the inhibitory function of the GABAergic system in the brain.
反复给予亚惊厥剂量的戊四氮(PTZ)可使大鼠对该化合物的作用产生渐进性敏感化(即化学性点燃)。使用两种不同的给药方案观察到PTZ诱导点燃的时间进程非常相似:1)每天注射一次(30mg/kg,腹腔注射),以及2)每隔一天注射一次(30mg/kg,腹腔注射)。当这些给药方案连续使用八周时,超过80%的大鼠在治疗结束时出现惊厥。相比之下,如果以15mg/kg的剂量每天腹腔注射两次PTZ,只有20%的大鼠产生敏感化。慢性治疗完成一年后,对PTZ惊厥作用的敏感性仍然增加。此外,用PTZ点燃的大鼠对由不同的中枢GABA能功能抑制剂诱导的惊厥表现出增强的易感性,如氯离子通道阻断剂印防己毒素、苯二氮䓬受体配体FG 7142和Ro 15-4513,以及GABA合成抑制剂异烟肼。相比之下,反复给予PTZ对甘氨酸受体拮抗剂士的宁惊厥作用的敏感性没有改变。提示PTZ产生的点燃可能与大脑中GABA能系统抑制功能的持续降低有关。