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抗癫痫药物和β-咔啉对兴奋性氨基酸诱发癫痫发作的不同作用。

Differential effects of antiepileptic drugs and beta-carbolines on seizures induced by excitatory amino acids.

作者信息

Turski L, Niemann W, Stephens D N

机构信息

Research Laboratories of Schering AG, Berlin, F.R.G.

出版信息

Neuroscience. 1990;39(3):799-807. doi: 10.1016/0306-4522(90)90262-3.

Abstract

Agonists acting at subtypes of glutamate receptors, N-methyl-D-aspartate, kainate and quisqualate, induce convulsions in rodents. Clonic seizures induced in mice by intracerebral administration of N-methyl-D-aspartate, kainate or quisqualate were used to study the anti- and proconvulsant potential of antiepileptic drugs and beta-carbolines. Systemic administration showed that the benzodiazepines clonazepam and midazolam blocked convulsions induced by kainate and had no effect on seizures triggered by N-methyl-D-aspartate and quisqualate. In contrast, diazepam blocked convulsions induced by either excitatory amino acid, as did valproate. The benzodiazepine receptor agonist beta-carboline ZK 93423 blocked convulsions induced by kainate but had no effect on seizures induced by N-methyl-D-aspartate or quisqualate. The antagonist beta-carboline ZK 93426 did not affect convulsions induced by excitatory amino acids, while the inverse agonists FG 7142 and ethyl-beta-carboline-3-carboxylate increased the sensitivity of mice to kainate. Phenobarbital and 2-chloroadenosine protected mice against seizures induced by quisqualate and kainate, while baclofen was active against convulsions produced by kainate. MK-801 selectively blocked convulsions induced by N-methyl-D-aspartate, and enhanced the susceptibility of mice to seizures triggered by kainate and quisqualate. Ethosuximide increased the susceptibility of mice to N-methyl-D-aspartate and had little or no effect on other types of seizures. Diphenylhydantoin enhanced the convulsant potential of quisqualate. Trimethadione and carbamazepine did not affect convulsions induced by N-methyl-D-aspartate, kainate or quisqualate. Intracerebral administration of midazolam protected mice against seizures induced by kainate. Ethosuximide increased the susceptibility of mice to N-methyl-D-aspartate, while diphenylhydantoin to quisqualate convulsions.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

作用于谷氨酸受体亚型(N-甲基-D-天冬氨酸、海人藻酸和使君子氨酸)的激动剂可在啮齿动物中诱发惊厥。通过脑内注射N-甲基-D-天冬氨酸、海人藻酸或使君子氨酸在小鼠中诱发阵挛性惊厥,用于研究抗癫痫药物和β-咔啉的抗惊厥和促惊厥潜力。全身给药显示,苯二氮䓬类药物氯硝西泮和咪达唑仑可阻断海人藻酸诱发的惊厥,对N-甲基-D-天冬氨酸和使君子氨酸引发的惊厥无影响。相比之下,地西泮可阻断由任何一种兴奋性氨基酸诱发的惊厥,丙戊酸也是如此。苯二氮䓬受体激动剂β-咔啉ZK 93423可阻断海人藻酸诱发的惊厥,但对N-甲基-D-天冬氨酸或使君子氨酸诱发的惊厥无影响。拮抗剂β-咔啉ZK 93426不影响兴奋性氨基酸诱发的惊厥,而反向激动剂FG 7142和乙基-β-咔啉-3-羧酸酯可增加小鼠对海人藻酸的敏感性。苯巴比妥和2-氯腺苷可保护小鼠免受使君子氨酸和海人藻酸诱发的惊厥,而巴氯芬对海人藻酸产生的惊厥有活性。MK-801可选择性阻断N-甲基-D-天冬氨酸诱发的惊厥,并增强小鼠对海人藻酸和使君子氨酸引发惊厥的易感性。乙琥胺增加小鼠对N-甲基-D-天冬氨酸的易感性,对其他类型的惊厥几乎没有影响。苯妥英增强使君子氨酸的惊厥潜力。三甲双酮和卡马西平不影响N-甲基-D-天冬氨酸、海人藻酸或使君子氨酸诱发的惊厥。脑内注射咪达唑仑可保护小鼠免受海人藻酸诱发的惊厥。乙琥胺增加小鼠对N-甲基-D-天冬氨酸的易感性,而苯妥英增加小鼠对使君子氨酸惊厥的易感性。(摘要截短至250字)

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