大麻二酚和氯硝西泮联合抗惊厥对条件性小鼠Dravet综合征的影响。

Shu-Hui Chuang, Ruth E Westenbroek, Nephi Stella, William A Catterall
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引用次数: 5

摘要

Dravet综合征(DS)是一种由编码脑i型电压门控钠通道Nav1.1的SCN1A基因杂合性功能丧失突变引起的严重儿童癫痫。退行性滑移是一种毁灭性的疾病,通常开始于6到9个月大的时候。症状包括复发性难治性癫痫发作和过早死亡,并伴有严重的神经精神合并症,包括多动、睡眠障碍、焦虑样行为、社会交往受损和认知缺陷。由于现有的治疗干预措施疗效差、不耐受或有其他副作用,因此对控制和治愈退行性痴呆的治疗方法的迫切需求尚未得到满足。本研究探讨了苯二氮卓类氯硝西泮(CLZ)与非精神药物大麻素大麻二酚(CBD)联合治疗条件性退行性痴呆小鼠热致热性惊厥的治疗潜力。我们的研究结果表明,低剂量的CLZ单独使用或与CBD联合使用可提高热诱导癫痫发作的阈值温度。与单独使用CLZ或单独使用CLZ相比,CLZ与CBD联合使用显著减少了癫痫发作持续时间,但不影响癫痫发作的严重程度,表明CLZ和CBD对癫痫发作持续时间的潜在叠加作用。我们的研究结果为支持CLZ和CBD联合治疗退行性痴呆热性惊厥提供了临床前证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Combined Antiseizure Efficacy of Cannabidiol and Clonazepam in a Conditional Mouse Model of Dravet Syndrome.

Combined Antiseizure Efficacy of Cannabidiol and Clonazepam in a Conditional Mouse Model of Dravet Syndrome.

Dravet Syndrome (DS) is a severe childhood epilepsy caused by heterozygous loss-of-function mutations in the SCN1A gene encoding brain type-I voltage-gated sodium channel Nav1.1. DS is a devastating disease that typically begins at six to nine months of age. Symptoms include recurrent intractable seizures and premature death with severe neuropsychiatric comorbidities, including hyperactivity, sleep disorder, anxiety-like behaviors, impaired social interactions, and cognitive deficits. There is an urgent unmet need for therapeutic approaches that control and cure DS, as available therapeutic interventions have poor efficacy, intolerance, or other side effects. Here we investigated the therapeutic potential of combining the benzodiazepine clonazepam (CLZ) with the nonpsychotropic phytocannabinoid cannabidiol (CBD) against thermally induced febrile seizures in a conditional mouse model of DS. Our results show that a low dose of CLZ alone or combined with CBD elevated the threshold temperature for the thermal induction of seizures. Combination of CLZ with CBD significantly reduced seizure duration compared to the vehicle or CLZ alone, but did not affect seizure severity, indicating potential additive actions of CLZ and CBD on the duration of seizures. Our findings provide preclinical evidence supporting combination therapy of CLZ and CBD for treatment of febrile seizures in DS.

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