Non-obvious effects of montelukast – leukotriene receptor blocker: frigoprotective and anticonvulsant properties

S. Shtrygol’, I. Kapelka, M. V. Mishchenko, O. Mishchenko
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引用次数: 3

Abstract

The participation of arachidonic acid metabolism products – prostaglandins and leukotrienes – in the process of inflammation is a common pathogenetic link of cold injury and epilepsy. Montelukast is widely used for the treatment of bronchial asthma and allergic rhinitis as a leukotriene receptor blocker. However, the mechanism of action of the drug suggests a wider range of its pharmacological properties and the corresponding scope of application. This study is aimed to determine the effectiveness of montelukast as a potential frigoprotective and anticonvulsant drug. Experiments were performed on 73 white mice weighing 20-22 g on models of acute general cooling and pentylenetetrazol convulsions. Frigoprotective properties were studied at a temperature of –18°C, recording the lifetime. Montelukast ("Singular", 2 mg/kg), acetylsalicylic acid ("Aspirin", 50 mg/kg), celecoxib ("Celebrex", 74 mg/kg), diclofenac sodium ("Voltaren", 14 mg/kg) were administered intragastrically as a suspension in a prophylactic mode, 30 minutes before the cold injury. In the study of anti­convulsant activity, montelukast ("Singular", 4 mg/kg) and sodium valproate ("Depakin", 300 mg/kg) were admi­nistered intragastrically 30 minutes before stimulating convulsions by subcutaneous administration of pentylene­tetrazole (90 mg/kg). The latent period of convulsions, the number of convulsions per 1 animal, % of mice with clonic and tonic paroxysms, the severity of convulsions in points, the duration of the convulsive period, the lifetime of animals and lethality were recorded for an hour. On the model of acute general cooling, montelukast showed a dose-dependent frigoprotective effect at a dose of 2 mg/kg surpassing drugs with proven frigoprotective properties – acetylsalicylic acid and celecoxib. On the model of pentylenetetrazole-induced convulsions, montelukast statistically significantly reduced the integral indicator of anticonvulsant activity – lethality – by 2.57 times. Thus, the experiment proved the significant role of leukotrienes in the pathogenesis of cold injury and epilepsy and justified the feasibility of further study of the frigoprotective and anticonvulsant properties of montelukast – leukotriene receptor blocker a drug as for adjuvant therapy, especially when these pathologies are combined with bronchial asthma and allergic rhinitis.
孟鲁司特-白三烯受体阻滞剂的非明显作用:抗冻和抗惊厥特性
花生四烯酸代谢产物-前列腺素和白三烯-参与炎症过程是冷损伤和癫痫的常见致病环节。孟鲁司特作为白三烯受体阻滞剂广泛用于支气管哮喘和变应性鼻炎的治疗。然而,药物的作用机制表明其具有更广泛的药理特性和相应的应用范围。本研究旨在确定孟鲁司特作为一种潜在的冷冻保护和抗惊厥药物的有效性。实验用体重20 ~ 22 g的73只小白鼠建立急性全身降温和戊四氮唑惊厥模型。在-18°C的温度下研究了其防冻性能,并记录了其寿命。孟鲁司特(“single”,2 mg/kg)、乙酰水杨酸(“阿司匹林”,50 mg/kg)、塞来昔布(“Celebrex”,74 mg/kg)、双氯芬酸钠(“伏他伦”,14 mg/kg)在冷伤前30分钟以预防方式灌胃。在抗惊厥活性研究中,孟鲁司特(“奇异”,4mg /kg)和丙戊酸钠(“Depakin”,300mg /kg)在刺激惊厥前30分钟灌胃,皮下给药戊四唑(90mg /kg)。1小时内记录惊厥潜伏期、每只动物惊厥次数、阵挛性和强直性发作小鼠的百分比、点惊厥严重程度、惊厥持续时间、动物寿命和死亡率。在急性全身降温模型中,孟鲁司特在2mg /kg的剂量下显示出剂量依赖性的冷冻保护作用,超过了具有已证实的冷冻保护特性的药物——乙酰水杨酸和塞来昔布。在戊四唑诱发惊厥模型中,孟鲁司特抗惊厥活性积分指标-致死率-降低了2.57倍,具有统计学意义。因此,本实验证明了白三烯在冷损伤和癫痫发病中的重要作用,也证明了进一步研究孟鲁司特-白三烯受体阻滞剂作为辅助治疗药物的低温保护和抗惊厥作用的可行性,特别是当这些疾病合并支气管哮喘和变应性鼻炎时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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