Department of Physiopathology, Institute of Agricultural Medicine, Jaczewskiego 2, PL 20-950 Lublin, Poland.
Pharmacol Rep. 2011;63(1):169-75. doi: 10.1016/s1734-1140(11)70412-1.
The objective of this study was to determine the effects of 7-nitroindazole (7NI--a preferential neuronal nitric oxide synthase (NOS) inhibitor) and NG-nitro-L-arginine (NNA--a non-selective NOS inhibitor) on the anticonvulsant action of pregabalin (PGB--a third-generation antiepileptic drug) in the maximal electroshock (MES)-induced seizure model in mice. Electroconvulsions were produced in mice by means of an alternating current (50 Hz, 500 V, 25 mA, ear-clip electrodes, 0.2 s stimulus duration, tonic hindlimb extension taken as the endpoint). The anticonvulsant action of PGB in the MES test was expressed as median effective doses (ED50 values) of the drug, protecting 50% of animals tested against MES-induced seizures. The acute adverse-effect potentials of PGB in combination with 7NI and NNA were evaluated in the chimney test (motor coordination), step-through passive avoidance task (long-term memory) and grip-strength test (skeletal muscular strength) in mice. 7NI (50 mg/kg, ip) significantly enhanced the anticonvulsant action of PGB by reducing the ED50 value of PGB from 145.0 mg/kg to 74.4 mg/kg (p<0.01). Similarly, 7NI at the lower dose of 25 mg/kg also potentiated the anticonvulsant action of PGB by lowering the ED50 value of PGB from 145.0 mg/kg to 117.9 mg/kg, although the results did not attain statistical significance. In contrast, NNA (40 mg/kg, ip) had no impact on the anticonvulsant effects of PGB. Moreover, none of the examined combinations of PGB with 7NI and NNA affected motor coordination, long-term memory and skeletal muscular strength in mice. Based on this preclinical study, one can conclude that 7NI significantly enhanced and NNA had no effect on the anticonvulsant activity of PGB against MES-induced seizures in mice.
本研究的目的是确定 7-硝基吲唑(7NI-一种优先的神经元型一氧化氮合酶(NOS)抑制剂)和 NG-硝基-L-精氨酸(NNA-一种非选择性 NOS 抑制剂)对普瑞巴林(PGB-第三代抗癫痫药物)在最大电休克(MES)诱导的惊厥模型中的抗惊厥作用的影响。通过交流电(50 Hz,500 V,25 mA,耳夹电极,0.2 s 刺激持续时间,以强直性后肢伸展作为终点)在小鼠中产生电惊厥。PGB 在 MES 测试中的抗惊厥作用表现为药物的中位数有效剂量(ED50 值),保护 50%接受测试的动物免受 MES 诱导的惊厥。在小鼠的烟囱测试(运动协调)、穿梭式被动回避任务(长期记忆)和握力测试(骨骼肌肉力量)中,评估了 PGB 与 7NI 和 NNA 联合使用的急性不良效应潜力。7NI(50 mg/kg,ip)通过将 PGB 的 ED50 值从 145.0 mg/kg 降低至 74.4 mg/kg(p<0.01),显著增强了 PGB 的抗惊厥作用。同样,7NI 低剂量 25 mg/kg 也通过将 PGB 的 ED50 值从 145.0 mg/kg 降低至 117.9 mg/kg,增强了 PGB 的抗惊厥作用,尽管结果没有达到统计学意义。相比之下,NNA(40 mg/kg,ip)对 PGB 的抗惊厥作用没有影响。此外,PGB 与 7NI 和 NNA 的组合在小鼠中均未影响运动协调、长期记忆和骨骼肌肉力量。基于这项临床前研究,可以得出结论,7NI 显著增强了 PGB 对 MES 诱导的惊厥的抗惊厥作用,而 NNA 则没有影响。