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An investigation of the antinociceptive effects of Riluzole in hyperal- gesia models of mice

机译:利鲁唑对痛觉过敏模型小鼠的镇痛作用研究

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摘要

Objective: To investigate the antinociceptive effects of Riluzole administered intraperitoneally in three hy-peralgesia model of mice. Methods: Antinociceptive tests in C57BL mice were investigated with formalin test acetic acid induced writhing test and tail-immersion test. The effects of intraperitoneally Riluzole 2 mg/kg, 4 mg/kg and 8 mg/kg on the pain threshold were observed. Result: We found that i.p. treatment with Riluzole (4 mg/kg and 8 mg/kg) blocked the second phase flinching behavior compared with vehicle (P < 0.05), but not during the first phase in the formalin test. In addition to the formalin test, Riluzole at different dose (from 2 to 8 mg/kg) attenuated acetic acid induced writhing response when compared to vehicle group (P < 0.05). In the tail-immersion test, Riluzole at the highest dose (8 mg/kg) caused significant increase in tail flick response latency as compared to vehicle animals or compared with Baseline (P < 0.05). Conclusion: Our results suggest that glu-tamate release inhibitor Riluzole can attenuate nociceptive behavior and has differrent antinociceptive characteristic according to the various pain models.
机译:目的:研究腹腔注射利鲁唑对三种高痛觉过敏小鼠的镇痛作用。方法:采用福尔马林试验,乙酸诱导的扭体试验和尾巴浸没试验研究C57BL小鼠的抗伤害感受试验。观察到腹膜内利鲁唑2 mg / kg,4 mg / kg和8 mg / kg对疼痛阈值的影响。结果:我们发现与媒介物相比,利鲁唑(4 mg / kg和8 mg / kg)治疗可阻止第二阶段的退缩行为(P <0.05),但在福尔马林测试的第一阶段则没有。除福尔马林测试外,与媒介物组相比,利鲁唑在不同剂量(2至8 mg / kg)下减弱了乙酸引起的扭体反应(P <0.05)。在尾巴浸没试验中,与媒介动物或基线相比,以最高剂量(8 mg / kg)的利鲁唑引起的甩尾反应潜伏期显着增加(P <0.05)。结论:我们的结果表明,根据各种疼痛模型,谷氨酸盐释放抑制剂利鲁唑可以减轻伤害感受,并具有不同的伤害感受特性。

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