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某些β-肾上腺素能受体拮抗剂对抗癫痫药物抗DBA/2小鼠听源性惊厥效力的影响。

Influence of some beta-adrenoceptor antagonists on the anticonvulsant potency of antiepileptic drugs against audiogenic seizures in DBA/2 mice.

作者信息

De Sarro Giovambattista, Di Paola Eugenio Donato, Ferreri Guido, De Sarro Angela, Fischer Wolfgang

机构信息

Department of Experimental and Clinical Medicine, Faculty of Medicine and Surgery, University of Catanzaro, Via T. Campanella, 115 Policlinico Mater Domini, 88100 Catanzaro, Italy.

出版信息

Eur J Pharmacol. 2002 May 10;442(3):205-13. doi: 10.1016/s0014-2999(02)01536-4.

Abstract

The two enantiomers of propranolol antagonize generalized tonic-clonic seizures in DBA/2 mice with the (-)-enantiomer being about 1.5 times more potent than the (+)-enantiomer. Metoprolol was less active and atenolol was unable to affect audiogenic seizures. In combination with conventional antiepileptic drugs, both propranolol enantiomers tested in doses not affecting the occurrence of audiogenic seizures increased the anticonvulsant activity of diazepam, phenobarbital, valproate and lamotrigine and tended to increase that of carbamazepine and phenytoin. The effect was more pronounced with the (-)-enantiomer. This increase was associated with an enhancement of motor impairment, however, the therapeutic index of combined treatment of the antiepileptic drugs with both propranolol enantiomers was more favourable than the combination with saline alone. Metoprolol was also able to decrease the ED(50) values of the antiepileptic drugs, whereas atenolol showed no effects. Since neither enantiomer of propranolol significantly influenced the total and free plasma levels of the antiepileptics, pharmacokinetic interactions are not likely. In addition, (+)- and (-)-propranolol did not significantly affect the hypothermic effects of the antiepileptics tested. In conclusion, both enantiomers of propranolol and metoprolol showed an additive anticonvulsant effect when co-administered with some conventional antiepileptic drugs, most notably diazepam, phenobarbital, lamotrigine and valproate, implicating a possible therapeutic relevance of such drug combinations.

摘要

普萘洛尔的两种对映体可拮抗DBA/2小鼠的全身强直阵挛性发作,其中(-)-对映体的效力约为(+)-对映体的1.5倍。美托洛尔的活性较低,阿替洛尔对听源性惊厥无影响。与传统抗癫痫药物联合使用时,两种普萘洛尔对映体在不影响听源性惊厥发生的剂量下,均可增强地西泮、苯巴比妥、丙戊酸和拉莫三嗪的抗惊厥活性,并倾向于增强卡马西平和苯妥英钠的抗惊厥活性。(-)-对映体的作用更为明显。这种增强与运动功能损害的加重有关,然而,抗癫痫药物与两种普萘洛尔对映体联合治疗的治疗指数比单独与生理盐水联合更有利。美托洛尔也能够降低抗癫痫药物的半数有效剂量(ED50),而阿替洛尔则无此作用。由于普萘洛尔的两种对映体均未显著影响抗癫痫药物的总血浆水平和游离血浆水平,因此不太可能存在药代动力学相互作用。此外,(+)-和(-)-普萘洛尔对所测试的抗癫痫药物的降温作用均无显著影响。总之,普萘洛尔的两种对映体和美托洛尔与一些传统抗癫痫药物联合使用时均显示出相加的抗惊厥作用,最显著的是地西泮、苯巴比妥、拉莫三嗪和丙戊酸,这表明这种药物组合可能具有治疗意义。

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