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钙在血管平滑肌中稳定细胞膜的机制。

Mechanism of membrane stabilization by calcium in vascular smooth muscle.

作者信息

Webb R C, Bohr D F

出版信息

Am J Physiol. 1978 Nov;235(5):C227-32. doi: 10.1152/ajpcell.1978.235.5.C227.

Abstract

In this study we observed relaxation in helical strips of rat tail artery in response to high concentrations of calcium after contraction induced by 10(-7) g/ml norepinephrine. This action of calcium on vascular smooth muscle contraction is referred to as the "membrane-stabilizing effect" of calcium. The current study demonstrates that changes caused by many of the variables that alter this relaxation induced by calcium parallel changes in relaxation in response to potassium; both are attenuated by ouabain, low sodium, reduced temperature, and low potassium. Relaxation produced by manganese is not similarly affected. Because potassium has been shown to cause relaxation of vascular smooth muscle by increasing the activity of sodium-potassium ATPase, we conclude that the relaxation produced by high concentrations of calcium is dependent on the activity of sodium-potassium ATPase; that produced by manganese is not.

摘要

在本研究中,我们观察到在10(-7) g/ml去甲肾上腺素诱导收缩后,大鼠尾动脉螺旋条对高浓度钙的反应出现松弛。钙对血管平滑肌收缩的这种作用被称为钙的“膜稳定效应”。当前研究表明,许多改变钙诱导的这种松弛的变量所引起的变化,与对钾反应的松弛变化相似;两者都被哇巴因、低钠、降低温度和低钾所减弱。锰产生的松弛不受类似影响。由于已表明钾通过增加钠钾ATP酶的活性引起血管平滑肌松弛,我们得出结论,高浓度钙产生的松弛依赖于钠钾ATP酶的活性;而锰产生的松弛则不依赖于此。

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