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首页> 外文期刊>Japanese Journal of Pharmacology >Long-Lasting Muscle Relaxant Activity of Eperisone Hydrochloride after Percutaneous Administration in Rats
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Long-Lasting Muscle Relaxant Activity of Eperisone Hydrochloride after Percutaneous Administration in Rats

机译:经皮给药后大鼠盐酸持久性松散的肌肉松弛活性

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References(7) Cited-By(12) Potency and duration of muscle relaxant activity of eperisone hydrochloride were examined after percutaneous administration in the intercollicular decerebrated rat rigidity model and compared to those of eperisone after intravenous injection. A continuous movement was loaded on the hindlimb of the rat model to maintain stable rigidity. The tonus of the hindlimb was recorded by EMG from the triceps surae and was quantified by using the public domain NIH Image program. Eperisone ointment administered percutaneously showed significant muscle relaxant activity at 8.4 cm2 (4.2 mg of eperisone) /rat. The effect was dose-dependent and lasted over 60 min. Intravenously injected eperisone showed significant activity at 1.25 mg/kg, but the decrease of tone was lost within 30 min after injection. Plasma eperisone levels were monitored in the same model, and they were well correlated to the dosage. These results suggest that percutaneously administered eperisone is absorbed efficiently and shows potent and long-lasting muscle relaxant activity.
机译:参考文献(7)引用(12)依匹乐松盐酸盐的大鼠肌肉僵硬模型经皮给药后检查了盐酸依哌酮的药效和肌肉松弛活性的持续时间,并将其与静脉注射后依匹立松的药效进行了比较。在大鼠模型的后肢上施加连续运动以保持稳定的刚度。 EMG记录了肱三头肌的后肢张力,并使用公共领域的NIH Image程序对其进行了定量。经皮给予的艾培瑞松软膏在8.4 cm2(4.2毫克艾培瑞松)/大鼠上显示出显着的肌肉松弛活性。效果是剂量依赖性的,持续超过60分钟。静脉注射的艾培瑞松在1.25 mg / kg时显示出显着的活性,但在注射后30分钟内音调下降消失。在同一模型中监测血浆艾培瑞松水平,它们与剂量密切相关。这些结果表明经皮给予的艾培瑞松可被有效吸收,并显示出有效且持久的肌肉松弛活性。

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