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细胞外镁离子浓度变化对大鼠门静脉电活动和机械活动的影响。

The effects of variations in extracellular magnesium concentration on electrical and mechanical activity in rat portal vein.

作者信息

Sigurdsson S B, Uvelius B

出版信息

Acta Physiol Scand. 1977 Mar;99(3):368-76. doi: 10.1111/j.1748-1716.1977.tb10390.x.

Abstract

The effects of various concentrations of extracellular Mg2+ on electrical and mechanical activity of the rat portal vein were studied. The integrated spontaneous contractile activity in the preparation was largest in Mg2+-free solution, decreased to about 50% at 1.2 mM Mg2+ and was almost completely abolished at 10 mM Mg2+. Each spontaneous contraction became smaller whereas contraction frequency was less affected. Sucrose gap recordings showed that the reduced spontaneous mechanical output was associated with decreased electrical activity on increasing [Mg2+]0. Increasing [K+]0 from 6 to 12 mM normalized the spontaneous mechanical activity in 10 mM Mg2+ solution. Local registration of electrical activity with 3 extracellular glass capillary electrodes showed that inactive areas developed at the high Mg2+ concentrations. These findings indicate that Mg2+ exerts a hyperpolarizing action on the smooth muscle cell membrane and, at the highest concentration, interferes with intercellular propagation. [Mg2+]0 in the range of 0-10 mM had no effect on the amplitude of K+ (122 mM) contractures at [Ca2+]0 greater than 0.5 mM. At [Ca2+]0 less than or equal to 0.5 the amplitude diminished with increasing [Mg2+]0. The latter observation indicates that Mg2+ can interfere with the Ca2+-permeability of the depolarized cell membrane. 1 mM EDTA in Na-tris 0 mM Mg2+ and 0 mM Ca2+ seemed to lower intracellular Mg2+ below the minimum concentration needed for contractile activity.

摘要

研究了不同浓度细胞外Mg2+对大鼠门静脉电活动和机械活动的影响。制备标本中的综合自发收缩活动在无Mg2+溶液中最大,在1.2 mM Mg2+时降至约50%,在10 mM Mg2+时几乎完全消失。每次自发收缩变小,而收缩频率受影响较小。蔗糖间隙记录显示,随着[Mg2+]0升高,自发机械输出降低与电活动减少相关。将[K+]0从6 mM增加到12 mM可使10 mM Mg2+溶液中的自发机械活动恢复正常。用3个细胞外玻璃毛细管电极进行电活动的局部记录显示,在高Mg2+浓度下会出现无活性区域。这些发现表明,Mg2+对平滑肌细胞膜发挥超极化作用,并且在最高浓度时会干扰细胞间的电传播。在[Ca2+]0大于0.5 mM时,0-10 mM范围内的[Mg2+]0对K+(122 mM)挛缩的幅度没有影响。在[Ca2+]0小于或等于0.5 mM时,幅度随[Mg2+]0升高而减小。后一观察结果表明,Mg2+可干扰去极化细胞膜的Ca2+通透性。在0 mM Mg2+和0 mM Ca2+的Na-三羟甲基氨基甲烷中加入1 mM EDTA似乎可使细胞内Mg2+降至收缩活动所需的最低浓度以下。

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