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非氨酯对苯二氮䓬耐受小鼠惊厥的拮抗作用及对GABA(A)受体功能增强的失败。

Antagonism of convulsions but failure to enhance GABA(A) receptor function by felbamate in mice tolerant to diazepam.

作者信息

Serra M, Cuccu R, Ghiani C A, Pisu M G, Murgia A, Biggio G

机构信息

Department of Experimental Biology B. Loddo, University of Cagliari, Italy.

出版信息

Neurochem Res. 1997 Jun;22(6):693-7. doi: 10.1023/a:1027349909655.

Abstract

The transfer of tolerance between drugs may indicate a common mode of action. The development of cross-tolerance to the anticonvulsant effect of felbamate after long-term treatment of mice with diazepam, a positive modulator of gamma-aminobutyric acid (GABA)-mediated transmission, was therefore studied in order to clarify the mechanism of this action of felbamate. A challenge injection of felbamate, administered 36 h after the last dose of chronic diazepam treatment, antagonized convulsions elicited by administration of isoniazid. In contrast, felbamate had no effect on the isoniazid-induced increase in t-[35S]butylbicyclophosphorothionate binding to cerebral cortical membranes of diazepam-tolerant mice. These results suggest that the action of felbamate on GABAergic transmission is not required for the anticonvulsant effect of this drug. This conclusion is consistent with studies that have indicated that the antiepileptic activity of felbamate depends on its modulatory activity at excitatory amino acid receptors.

摘要

药物之间耐受性的转移可能表明存在共同的作用模式。因此,为了阐明非氨酯这种作用的机制,研究了用γ-氨基丁酸(GABA)介导传递的阳性调节剂地西泮长期治疗小鼠后,小鼠对非氨酯抗惊厥作用产生交叉耐受性的情况。在慢性地西泮治疗的最后一剂后36小时给予非氨酯激发注射,可对抗异烟肼给药引起的惊厥。相反,非氨酯对异烟肼诱导的地西泮耐受小鼠大脑皮质膜上t-[35S]丁基双环磷硫酯结合增加没有影响。这些结果表明,非氨酯对GABA能传递的作用并非该药物抗惊厥作用所必需。这一结论与表明非氨酯的抗癫痫活性取决于其对兴奋性氨基酸受体的调节活性的研究一致。

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