[在两栖动物离体神经肌肉制剂中,4-甲基己甲醇诱导的破伤风反应的促进作用]。

Acta vitaminologica et enzymologica Pub Date : 1985-01-01
R Aragno, V Bettini, L De Bartolomeis, P Fabro, P Ton, L Munari
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引用次数: 0

摘要

先前的观察表明,当运动、躯体和自主神经末梢受到刺激时,4-甲基肌肉素(4ME)和钙引起的反应增加。在本研究中,我们研究了生物类黄酮和增加培养基[Ca++]对离体青蛙“坐骨神经-腓肠肌”制备的破伤风反应的影响。4ME总是促进完全破伤风反应的开始,也经常增加已发展的机械张力。当生物类黄酮与抗坏血酸一起使用时,这些效果更为明显。此外,增加的介质[Ca++]也引起了类似的效果。硝苯地平和氟桂利嗪是著名的钙离子拮抗剂,它们不断降低甚至消除生物类黄酮诱导的促进作用。基于这些结果,我们可以假设这些观察到的促进作用依赖于增加的疼痛释放和增加的肌肉机械效率。我们之前的结果和一些文献数据表明,这些影响可能是由于Ca++通过运动神经末梢和肌肉纤维细胞膜的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Facilitation of the onset of tetanic responses induced by 4-methylesculetol in amphibian isolated neuromuscular preparations].

Previous observations have shown that the 4-Methylesculetin (4ME) and the calcium provoke an increased response when the motor somatic and autonomic nerve-endings are stimolated. In the present research, we have studied the influence of the bioflavonoid and of an increased medium [Ca++] on the tetanic responses obtained from the isolated frog "sciatic nerve-gastrocnemius muscle" preparation. The 4ME has always facilitated the beginning of a complete tetanic response and has also frequently increased the developed mechanical tension. These effects appeared more evident when the bioflavonoid was employed together with the ascorbic acid. Moreover, an increased medium [Ca++] has induced similar effects. The nifedipine and the flunarizine, well-known Ca++ -antagonists, have constantly reduced or even abolished the facilitating effect induced by the bioflavonoid. On the basis of these results, we could hypothize that these observed facilitating effects are dependent on both an increased Ach-release and an increased muscle mechanical efficiency. Our previous results and also some literature data suggest that these effects could be due to an increased Ca++-passage through the cell membrane of the motor nervendings and of the muscle fibres too.

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