Dichtl A, Vierling W
Institut für Pharmakologie und Toxikologie, Technischen Universität München, F.R.G.
Eur J Pharmacol. 1991 Nov 12;204(3):243-8. doi: 10.1016/0014-2999(91)90848-k.
It was investigated whether the negative inotropic effect of magnesium in mammalian heart ventricular muscle is due to inhibition of the calcium inward current. Whole-cell voltage-clamp experiments were carried out with isolated guinea-pig heart cells. The sodium inward current was inactivated by a conditioning pre-pulse or by addition of tetrodotoxin. Magnesium concentration dependently and reversibly diminished the calcium inward current (by about 45% after an increase in magnesium concentration, from 1.2 to 9.6 mM). The decrease was mainly due to diminution of the maximally available calcium inward current but was additionally due to a shift of the current-voltage relationship to more positive potentials. The crucial dependence of the inhibition of the inward current on the pre-pulse potential was demonstrated. Conditioning depolarization to potentials more negative than -40 mV led to an increase of an inward current by magnesium. This was probably the consequence of incomplete inactivation of the sodium current and the shift of its current-voltage relationship by the divalent cation.
研究了镁对哺乳动物心室肌的负性肌力作用是否归因于抑制钙内向电流。使用分离的豚鼠心脏细胞进行全细胞电压钳实验。通过预处理脉冲或添加河豚毒素使钠内向电流失活。镁浓度依赖性且可逆地减少钙内向电流(镁浓度从1.2 mM增加到9.6 mM后,钙内向电流减少约45%)。这种减少主要是由于最大可利用钙内向电流的减小,但也归因于电流-电压关系向更正电位的偏移。证明了内向电流抑制对预处理脉冲电位的关键依赖性。将预处理去极化至比-40 mV更负的电位会导致镁使内向电流增加。这可能是钠电流不完全失活及其电流-电压关系被二价阳离子偏移的结果。