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大鼠皮质部位之间的抗癫痫敏感性差异

Differential antiepileptic sensitivity between cortical sites in the rat.

作者信息

Moss K A, Kalichman M W, Iragui V J

出版信息

Epilepsia. 1986 May-Jun;27(3):209-14. doi: 10.1111/j.1528-1157.1986.tb03530.x.

Abstract

The relative efficacies of phenobarbital (PB), phenytoin (PHT), carbamazepine (CBZ), and valproic acid (VPA) in the suppression of focal and generalized seizures produced by electrical stimulation of two different cortical sites (areas 3 and 10) were evaluated in the rat. The two cortical sites were distinguished by significantly different dose-response curve slopes for the suppression of afterdischarge duration by PHT, CBZ and VPA, which suggests more than one mechanism of action for these drugs. The dose-response curve slopes for PB, on the contrary, were not significantly different, although its potency was significantly greater in area 10. For suppression of generalized convulsions, dose-response curve slopes were not significantly different for any of the drugs. Potencies of PHT, CBZ and VPA were equivalent in the two areas, but PB was significantly more potent in the suppression of generalized convulsions triggered from area 10. It is concluded that focal seizures elicited by the stimulation of different cortical sites are differentially refractory to antiepileptic drugs.

摘要

在大鼠中评估了苯巴比妥(PB)、苯妥英(PHT)、卡马西平(CBZ)和丙戊酸(VPA)对电刺激两个不同皮质部位(3区和10区)所产生的局灶性和全身性癫痫发作的抑制效果。这两个皮质部位在PHT、CBZ和VPA抑制后放电持续时间方面具有显著不同的剂量-反应曲线斜率,这表明这些药物存在不止一种作用机制。相反,PB的剂量-反应曲线斜率没有显著差异,尽管其在10区的效力明显更高。对于全身性惊厥的抑制,任何一种药物的剂量-反应曲线斜率均无显著差异。PHT、CBZ和VPA在这两个区域的效力相当,但PB在抑制由10区引发的全身性惊厥方面明显更有效。得出的结论是,刺激不同皮质部位引发的局灶性癫痫发作对抗癫痫药物的难治性存在差异。

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