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首页> 外文期刊>Japanese Journal of Pharmacology >POTENTIATION OF INDIRECTLY INDUCED MUSCLE TWITCHES BY ORGANIC CALCIUM ANTAGONISTS IN PHRENIC NERVE-DIAPHRAGM MUSCLE PREPARATIONS OF MICE
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POTENTIATION OF INDIRECTLY INDUCED MUSCLE TWITCHES BY ORGANIC CALCIUM ANTAGONISTS IN PHRENIC NERVE-DIAPHRAGM MUSCLE PREPARATIONS OF MICE

机译:用膈神经隔膜肌制剂的有机钙拮抗剂间接诱导肌肉抽搐的增强

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References(16) Cited-By(2) Organic calcium antagonists (l- and d-verapamil, D600, and diltiazem) were examined for their effects on muscle twitches of isolated phrenic nerve-diaphragm muscle preparations of mice. The calcium antagonists (1×10-6 to 7.5×10-5 M) increased the amplitude of muscle twitches induced by nerve stimuli with short durations (0.04 to 0.4 msec) of rectangular pulses. However, these agents were poorly effective on twitches induced by nerve stimuli with longer durations over 0.6 msec or by direct shocks. The potentiative effect was reversible, reproducible and dependent on their concentrations. Diltiazem was the most effective among the four agents tested. The twitch increase produced by all of the agents was demonstrated at concentrations of external Ca++ above 0.6 mM. At Ca++ concentrations below 0.5 mM, the tension of the indirectly induced muscle twitch was partially inhibited in the presence of these agents. Caffeine, theophylline, isoproterenol or hypertonic potassium ions increased the tension of indirectly induced muscle twitches. The potentiative effect of the organic calcium antagonists, however, was discriminated from those induced by the other agents under some conditions. From these results, it is suggested that the organic calcium antagonists alter the reactivity of the preparation to nerve shock. The potentiative effect of the agents on indirectly induced muscle twitch may include an increase in the number of fibers contracting per nerve impulse through increasing transmitter release from the nerve terminal, but not an increase in contractility of an individual muscle fiber.
机译:研究参考(16)被引用(2)有机钙拮抗剂(L-和D-Verapamil,D600和Diltiazem)对小鼠分离的膈神经隔膜肌制剂的肌肉抽搐作用。钙拮抗剂(1×10-6至7.5×10-5米)增加了神经刺激诱导的肌肉抽搐幅度,短持续时间(0.04至0.4毫秒)的矩形脉冲。然而,这些试剂对神经刺激诱导的抽搐有效,持续时间超过0.6毫秒或通过直接冲击。增强效果是可逆,可重复的,依赖于其浓度。 Diltiazem在测试的四种药剂中是最有效的。通过所有试剂产生的抽搐增加以高于0.6mm的外部Ca ++的浓度证明。在0.5mm以下的Ca ++浓度下,间接诱导的肌肉抽搐的张力在这些试剂存在下部分抑制。咖啡因,茶碱,异丙肾或高渗钾离子增加了间接诱导的肌肉抽搐的张力。然而,有机钙拮抗剂的增强作用被不同于某些条件下由其他药剂诱导的效果。从这些结果来看,有机钙拮抗剂的表明,有机钙拮抗剂改变了制剂的反应性令神经休克。药剂对间接诱导的肌肉抽搐的增强效果可以包括通过增加来自神经末端的发射器释放的每根神经脉冲的纤维数量增加,但不是单个肌纤维的收缩性的增加。

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