Glenn W, Kerrick L, Donaldson S K
Pflugers Arch. 1975 Jul 28;358(3):195-201. doi: 10.1007/BF00587216.
The effects of intracellular Mg2+ on Ca2+-activated isometric tension generation in rat cardiac muscle fibers and frog skeletal muscle were compared. The membranous sarcolemmal barrier was removed from rat cardiac muscle fibers by mechanical disruption and from frog skeletal muscle by skinning. Tension was recorded in the fibers in bathing solutions of different Ca2+ concentrations and either 5 X 10(-5) M or 1 X 10(-3) M Mg2+ concentration (the same concentrations used in a previous study on single skinned frog skeletal muscle fibers [3]). The amount of Ca2+ required to activate the muscle increased with Mg2+ concentration for both rat ventricular muscle and frog skeletal muscle. These data indicate that intracellular Mg2+ concentration could strongly modulate Ca2+-activated tension in cardiac muscle and that very similar molecular mechanisms are responsible for Ca2+-activated tension in rat ventricular muscle and frog skeletal muscle. The possible sites of action of Mg2+ on Ca2+-activated tension are discussed.
比较了细胞内Mg2+对大鼠心肌纤维和青蛙骨骼肌中Ca2+激活的等长张力产生的影响。通过机械破坏去除大鼠心肌纤维的膜性肌膜屏障,通过去皮去除青蛙骨骼肌的膜性肌膜屏障。在不同Ca2+浓度以及5×10(-5)M或1×10(-3)M Mg2+浓度(与先前对单个去皮青蛙骨骼肌纤维的研究[3]中使用的浓度相同)的浴液中记录纤维中的张力。对于大鼠心室肌和青蛙骨骼肌,激活肌肉所需的Ca2+量随Mg2+浓度的增加而增加。这些数据表明,细胞内Mg2+浓度可强烈调节心肌中Ca2+激活的张力,并且非常相似的分子机制负责大鼠心室肌和青蛙骨骼肌中Ca2+激活的张力。讨论了Mg2+对Ca2+激活张力的可能作用位点。