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首页> 外文期刊>General Physiology and Biophysics >Etifoxine does not impair muscle tone and motor function in rats as assessed by in vivo and in vitro methods
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Etifoxine does not impair muscle tone and motor function in rats as assessed by in vivo and in vitro methods

机译:在体内和体外方法评估的大鼠中,乙烯氧胺在大鼠中并不损害肌肉色调和运动功能

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The purpose of our study is to evaluate the effects of the translocator protein (TSPO) ligand etifoxine on muscle tone and locomotor activity. In addition, the mechanism of action of etifoxine on the presynaptic membrane and neuromuscular junction is investigated. These effects of etifoxine were examined employing the following methods: 1) in vivo experiments using bar holding test and activity cage test, and 2) comparative in vitro studies with nifedipine on indirectly-elicited twitches of striated abdominal muscle preparations. Etifoxine in doses 50 mg/kg and 100 mg/kg i.p. does not produce any significant changes in locomotor activity and muscle tone of intact rats. Nifedipine (10(-5) M) induces a significant decrease in the muscle force of striated muscle preparations. Etifoxine (10(-8)-10(-4) M) has no significant effect on indirectly-elicited twitch tension. Results show that the TSPO ligand etifoxine has no myorelaxant effect. The activation of TSPO is not associated with a reduction in muscle tone and motor impairment. Etifoxine does not affect the presynaptic membrane and its influence on L-type Ca2+-channelsis insignificant. Etifoxine does not act as a competitive antagonist of acetylcholine and does not impair the impulse transmission in the neuromuscular junction.
机译:我们的研究目的是评估译备器蛋白(TSPO)配体烯胺对肌肉间距和运动活性的影响。此外,研究了烯肟胺对突触前膜和神经肌肉结的作用机制。研究了烯嗪的这些效果采用以下方法:1)使用棒保持试验和活性笼试验的体内实验,以及2)与硝苯地平对脉肌制剂间接引发的抽搐进行硝苯地平的比较体外研究。乙烯肟剂量为50mg / kg和100mg / kg i.p.不会产生适应性大鼠的运动活性和肌肉口的任何显着变化。硝苯地平(10(-5)m)诱导肌肉制剂的肌肉力的显着降低。烯嗪(10(-8)-10(-4)m)对间接引发的抽搐张力没有显着影响。结果表明,TSPO配体etifoxine没有蒙着蒙茂效果。 TSPO的激活与肌肉音调和电机损伤的降低无关。乙烯干含量不影响突触膜及其对L型Ca2 + -Channelsis微不足道的影响。硫舒胺不作为乙酰胆碱的竞争性拮抗剂,不会损害神经肌肉交配中的脉冲传播。

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