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首页> 外文期刊>British Journal of Pharmacology >The effect of L-type calcium channel modulators on the mobilization of intracellular calcium stores in guinea-pig intestinal smooth muscle
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The effect of L-type calcium channel modulators on the mobilization of intracellular calcium stores in guinea-pig intestinal smooth muscle

机译:L型钙通道调节剂对豚鼠小肠平滑肌细胞内钙存储动员的影响

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摘要

1 The action of Ca~(2+) channel modulators has been examined on the intracellular Ca~(2+) signal in the longitudinal smooth muscle cells of the guinea-pig intestine after exposure to histamine and to agents known to affect intracellular Ca~(2+) stores. Isometric contraction has been measured simultaneously with front-surface fluorometry of fura 2-loaded preparations. 2 Histamine (10 μM) evoked a phasic and tonic increase in [Ca~(2+)]_i and contraction which were both sensitive to the Ca~(2+) channel blockers, nimodipine and D600. 3 Caffeine (10 mM) evoked in rapid increase in [Ca~(2+)]_i which was sustained as long as the preparation was exposed to the drug, whereas the contractile response was only phasic. In the presence of nimodipine 1 μM, the phasic contraction was absent although the fura 2-Ca~(2+) signal amounted to 32% of the control.
机译:1已检查了Ca〜(2+)通道调节剂对暴露于组胺和已知会影响细胞内Ca〜(〜)的豚鼠肠道纵向平滑肌细胞中Ca〜(2+)信号的作用(2+)家商店。等轴测收缩与呋喃2装制剂的正面荧光法同时进行了测量。 2组胺(10μM)引起[Ca〜(2 +)] _ i的阶段性和强直性增加和收缩,这两个都对Ca〜(2+)通道阻滞剂,尼莫地平和D600敏感。 3咖啡因(10 mM)引起[Ca〜(2 +)] _ i快速增加,只要将制剂暴露于药物,这种咖啡因就会持续存在,而收缩反应只是阶段性的。在存在尼莫地平1μM的情况下,尽管呋喃2-Ca〜(2+)信号占对照的32%,但没有相收缩。

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