首页> 外文期刊>Japanese Journal of Pharmacology >Depolarizing Effects of Glycyrrhizin-Derivatives Relating to the Blend Effects with Paeoniflorin in Mouse Diaphragm Muscle
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Depolarizing Effects of Glycyrrhizin-Derivatives Relating to the Blend Effects with Paeoniflorin in Mouse Diaphragm Muscle

机译:甘草酸衍生物的去极化作用与Blend药苷在小鼠Mouse肌中的混合作用有关

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References(7) Cited-By(14) Glycyrrhizin (GLR) and its newly synthesized derivatives, deoxoglycyrrhetol dihemisuccinate (I), deoxoglycyrrhetol dihemiphthalate (II), and the related compounds, carbenoxolone and glycyrrhetinic acid hemiphthalate (III), were assayed with or without paeoniflorin (PF) in mice diaphragm muscles. GLR-derivatives per se blocked the nerve-stimulated twitch tensions with the following order of potencies: carbenoxolone=IIIII=IGLR. The potencies paralleled the extent of muscle depolarization except in the case of I. GLR and I only increased muscle conductance. The blocking effects by GLR-derivat!ves per se on twitch responses are, therefore, can be explained by depolarization of muscle membranes and not by membrane conductance change. When carbenoxolone, II or GLR were blended with PF, the potentiation of the blocking effects observed may be related to the muscle depolarization rather than by the increase in membrane conductance.
机译:参考文献(7)被引用的By(14)甘草甜素(GLR)及其新合成的衍生物,去氧甘草酸二半琥珀酸酯(I),去氧甘草酸二半邻苯二甲酸酯(II)以及相关化合物羧苄索酮和甘草次酸半邻苯二甲酸酯(III)的含量进行了分析。小鼠diaphragm肌中不含pa药苷(PF)。 GLR衍生物本身以下列效力顺序阻断了神经刺激的抽搐张力:羧甲酮= III> II = I> GLR。除I. GLR和I的情况外,效力与肌肉去极化的程度平行。因此,GLR衍生物本身对抽搐反应的阻滞作用可以通过肌膜去极化而非膜电导变化来解释。当将羧苄酮,II或GLR与PF混合时,观察到的阻断作用的增强可能与肌肉去极化有关,而不是与膜电导的增加有关。

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