Department of Science of Health, School of Medicine and Surgery, University "Magna Graecia" of Catanzaro, Italy.
Department of Science of Health, School of Medicine and Surgery, University "Magna Graecia" of Catanzaro, Italy.
Epilepsy Res. 2018 Oct;146:94-102. doi: 10.1016/j.eplepsyres.2018.07.018. Epub 2018 Aug 1.
Tolerance to some therapeutic effects of antiepileptic drugs may account for the development of pharmacoresistance in patients with epilepsy. In the present study, following oral acute pretreatment with the new antiepileptic drug perampanel (0.1, 0.3, 1 or 3 mg/kg), we observed that the drug significantly and dose-dependently attenuated the seizure phases (clonus and tonus) of audiogenic seizures in genetically epilepsy prone rats (GEPR-9 s), a genetic model of reflex generalized epilepsy. In addition, the GEPR-9 s were administered orally with perampanel (1 or 3 mg/kg) once daily for 10 weeks in order to study the possible development of tolerance, and when animals were subjected to auditory stimulation we observed that the ED values against clonus or tonus were not significantly different from those observed after single administration. Furthermore, the duration of anticonvulsant effects observed between 60 min and 9 h following oral administration of perampanel (1 mg/kg) were similar in acute and after chronic treatment. In another group of experiments, clobazam (0.75, 1.5, 3, 6, 9, 12 and 15 mg/kg) after acute administration was able to dose-dependently reduce the severity of the audiogenic seizures in GEPR-9 s. When clobazam (6 or 12 mg/kg) was administered alone for 10 consecutive weeks a clear development of tolerance to its anticonvulsant effects within approximately seven weeks was observed. In addition, we observed that when clobazam (6 mg/kg) was co-administered with perampanel (1 mg/kg), the latter drug was able to attenuate the development of tolerance to the antiseizure activity of clobazam. The present data indicate that both perampanel and clobazam are effective against audiogenic seizures, however, clobazam effects are hampered by the development of tolerance. Furthermore, concomitant treatment with perampanel slows development of tolerance to the anticonvulsant effects of clobazam in GEPR-9 s.
抗癫痫药物的一些治疗效果的耐受性可能是癫痫患者出现药物抵抗的原因。在本研究中,我们观察到新的抗癫痫药物吡仑帕奈(0.1、0.3、1 或 3mg/kg)经口服急性预处理后,可显著且剂量依赖性地减弱听觉诱导性癫痫发作的癫痫发作阶段(阵挛和强直)在遗传易患癫痫大鼠(GEPR-9s)中,这是一种反射性全身性癫痫的遗传模型。此外,GEPR-9s 每天口服吡仑帕奈(1 或 3mg/kg)10 周,以研究可能出现的耐受性,当动物受到听觉刺激时,我们观察到对阵挛或强直的 ED 值与单次给药后观察到的 ED 值没有显著差异。此外,在口服吡仑帕奈(1mg/kg)后 60min 至 9h 之间观察到的抗惊厥作用持续时间在急性和慢性治疗后相似。在另一组实验中,急性给予氯巴占(0.75、1.5、3、6、9、12 和 15mg/kg)后,可剂量依赖性地降低 GEPR-9s 听觉诱导性癫痫发作的严重程度。当氯巴占(6 或 12mg/kg)连续 10 周单独给药时,大约 7 周内观察到其抗惊厥作用明显出现耐受性。此外,我们观察到当氯巴占(6mg/kg)与吡仑帕奈(1mg/kg)联合给药时,后者药物能够减轻氯巴占抗癫痫作用的耐受性发展。目前的数据表明,吡仑帕奈和氯巴占均对听觉诱导性癫痫发作有效,然而,氯巴占的作用受到耐受性发展的阻碍。此外,同时给予吡仑帕奈可减缓 GEPR-9s 中氯巴占抗惊厥作用的耐受性发展。