Neurosurg Focus. 2019 Mar 1;46(3):E6. doi: 10.3171/2019.1.FOCUS18596.
OBJECTIVERiluzole is a glutamatergic modulator that has recently shown potential for neuroprotection after spinal cord injury (SCI). While the effects of riluzole are extensively documented in animal models of SCI, there remains heterogeneity in findings. Moreover, there is a paucity of data on the pharmacology of riluzole and its effects in humans. For the present study, the authors systematically reviewed the literature to provide a comprehensive understanding of the effects of riluzole in SCI.METHODSThe PubMed database was queried from 1996 to September 2018 to identify animal studies and clinical trials involving riluzole administration for SCI. Once articles were identified, they were processed for year of publication, study design, subject type, injury model, number of subjects in experimental and control groups, dose, timing/route of administration, and outcomes.RESULTSA total of 37 studies were included in this study. Three placebo-controlled clinical trials were included with a total of 73 patients with a mean age of 39.1 years (range 18-70 years). For the clinical trials included within this study, the American Spinal Injury Association Impairment Scale distributions for SCI were 42.6% grade A, 25% grade B, 26.6% grade C, and 6.2% grade D. Key findings from studies in humans included decreased nociception, improved motor function, and attenuated spastic reflexes. Twenty-six animal studies (24 in vivo, 1 in vitro, and 1 including both in vivo and in vitro) were included. A total of 520 animals/in vitro specimens were exposed to riluzole and 515 animals/in vitro specimens underwent other treatment for comparison. The average dose of riluzole for intraperitoneal, in vivo studies was 6.5 mg/kg (range 1-10 mg/kg). Key findings from animal studies included behavioral improvement, histopathological tissue sparing, and modified electrophysiology after SCI. Eight studies examined the pharmacology of riluzole in SCI. Key findings from pharmacological studies included riluzole dose-dependent effects on glutamate uptake and its modified bioavailability after SCI in both animal and clinical models.CONCLUSIONSSCI has many negative sequelae requiring neuroprotective intervention. While still relatively new in its applications for SCI, both animal and human studies demonstrate riluzole to be a promising pharmacological intervention to attenuate the devastating effects of this condition.
利鲁唑是一种谷氨酸调节剂,最近在脊髓损伤(SCI)后显示出神经保护作用。虽然利鲁唑在 SCI 的动物模型中得到了广泛的研究,但研究结果仍存在异质性。此外,关于利鲁唑的药理学及其在人体中的作用的数据很少。本研究作者系统地综述了文献,以全面了解利鲁唑在 SCI 中的作用。
从 1996 年至 2018 年 9 月,检索 PubMed 数据库以确定涉及利鲁唑治疗 SCI 的动物研究和临床试验。一旦确定了文章,就会对其出版年份、研究设计、研究对象类型、损伤模型、实验组和对照组的研究对象数量、剂量、给药时间/途径以及结果进行处理。
本研究共纳入 37 项研究。其中包括 3 项安慰剂对照临床试验,共纳入 73 例患者,平均年龄 39.1 岁(18-70 岁)。在本研究纳入的临床试验中,美国脊髓损伤协会损伤分级(ASIA)分布为 42.6%为 A 级,25%为 B 级,26.6%为 C 级,6.2%为 D 级。来自人类研究的主要发现包括疼痛减轻、运动功能改善和痉挛反射减弱。纳入 26 项动物研究(24 项体内研究、1 项体外研究和 1 项同时包括体内和体外研究)。520 只动物/体外标本接受利鲁唑治疗,515 只动物/体外标本接受其他治疗作为对照。腹腔内注射的利鲁唑平均剂量为 6.5mg/kg(1-10mg/kg)。动物研究的主要发现包括行为改善、组织病理 spared 和 SCI 后电生理学改变。8 项研究检查了利鲁唑在 SCI 中的药理学。药理研究的主要发现包括利鲁唑剂量依赖性对谷氨酸摄取的影响及其在动物和临床模型中 SCI 后的生物利用度改变。
SCI 有许多需要神经保护干预的不良后果。尽管利鲁唑在 SCI 中的应用仍然相对较新,但动物和人体研究都表明利鲁唑是一种有前途的药物干预措施,可以减轻这种疾病的破坏性影响。