Buchweitz O, Bianchi C P
Department of Pharmacology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Life Sci. 1994;55(23):1853-61. doi: 10.1016/0024-3205(94)90096-5.
Initial magnesium transport in low magnesium Ringer in the frog myocardium consists of at least two systems, a fast system with high capacity with a time constant of 30 seconds and a slow transport system that operates with a time constant of 165 seconds. Both transport systems appear to be electroneutral and can operate either against an electrochemical gradient or with an electrochemical gradient. The fast transport system can transport Mg2+ in an outward direction at 1.84 p mol cm-2 sec-1; the slow system causes Mg2+ to be transported outward at 0.05 p mol cm-2 sec-1. Gramicidin S (5 microM) decreases the slow outward transport system to 0.01 p mol cm-2 sec-1 and at concentrations greater than 1 microM inhibits not only slow magnesium outflux in low calcium Ringer but also inhibits magnesium influx during recovery of Mg2+ in Ringer. Gramicidin S at 5 microM decreases Mg2+ influx from .04 p mol cm-2 sec-1 to 0.01 p mol cm2 sec-1 indicating that influx and efflux may take place on the same transport system. In the presence of 10 mM Mg2+ Gramicidin S increases magnesium content. Epinephrine increases magnesium efflux and overcomes the inhibition of Mg2+ efflux by Gramicidin S.
蛙心肌低镁林格液中的初始镁转运至少由两个系统组成,一个是高容量的快速系统,时间常数为30秒,另一个是慢速转运系统,时间常数为165秒。这两个转运系统似乎都是电中性的,既可以逆电化学梯度运行,也可以顺电化学梯度运行。快速转运系统能以1.84皮摩尔·厘米⁻²·秒⁻¹的速度向外转运Mg²⁺;慢速系统使Mg²⁺以0.05皮摩尔·厘米⁻²·秒⁻¹的速度向外转运。短杆菌肽S(5微摩尔)将慢速向外转运系统降至0.01皮摩尔·厘米⁻²·秒⁻¹,且在浓度大于1微摩尔时,不仅抑制低钙林格液中镁的慢速外流,还抑制林格液中Mg²⁺恢复过程中的镁内流。5微摩尔的短杆菌肽S将Mg²⁺内流从0.04皮摩尔·厘米⁻²·秒⁻¹降至0.01皮摩尔·厘米⁻²·秒⁻¹,这表明内流和外流可能发生在同一转运系统上。在存在10毫摩尔Mg²⁺的情况下,短杆菌肽S会增加镁含量。肾上腺素会增加镁外流,并克服短杆菌肽S对Mg²⁺外流的抑制作用。