Krause S M
Department of Physiology, Jefferson Medical College, Philadelphia, Pennsylvania 19107.
Am J Physiol. 1991 Jul;261(1 Pt 2):H229-35. doi: 10.1152/ajpheart.1991.261.1.H229.
Intracellular free Mg2+ concentration [( Mg2+]i) has been shown to increase markedly during ischemia from 0.6 to 3.2 mM and remain elevated severalfold at 1.5 mM after reperfusion of the stunned heart. The significance of this rise in [Mg2+]i after reperfusion on cellular function is not well known. To determine whether this increase in free [Mg2+] would alter the function of the sarcoplasmic reticulum (SR), the effects of an increase in free [Mg2+] on the SR Ca(2+)-dependent Mg(2+)-adenosinetriphosphatase (ATPase) activity were examined in SR isolated from Langendorff-perfused, isovolumic rabbit hearts after 15 min of reversible ischemia (global stunning). Oxalate-supported Ca2+ transport, assessed under identical conditions (0.4 mM free Mg2+, 15 microM free Ca2+), was reduced from 495 +/- 29 to 395 +/- 27 nmol Ca2+.mg protein-1.min-1 in control and stunned hearts, respectively, indicating a defect in enzyme function. This defect was confirmed by a decrease in the maximal Ca(2+)-dependent Mg(2+)-ATPase activity. An increase in the free [Mg2+] to simulate conditions after reperfusion leads to a decrease in the Ca2+ sensitivity of the SR Mg(2+)-ATPase. Fifty percent activation was shifted from a control free [Ca2+] of 0.42 microM at 0.6 mM free [Mg2+] to 0.63 microM free [Ca2+] at 1.2 mM free [Mg2+], conditions that simulate the reperfused stunned myocardium. These results indicate that after stunning the observed decline in SR Ca2+ transport, determined under similar incubation conditions, may be further jeopardized by the sustained increase in free [Mg2+].(ABSTRACT TRUNCATED AT 250 WORDS)
细胞内游离镁离子浓度[Mg2+]i在缺血期间已显示出显著增加,从0.6毫摩尔升至3.2毫摩尔,并且在顿抑心脏再灌注后以1.5毫摩尔的水平保持数倍升高。再灌注后[Mg2+]i的这种升高对细胞功能的意义尚不清楚。为了确定游离[Mg2+]的这种增加是否会改变肌浆网(SR)的功能,在15分钟可逆性缺血(整体顿抑)后,从Langendorff灌注的等容兔心脏分离出的SR中,研究了游离[Mg2+]增加对SR钙依赖性镁离子三磷酸腺苷酶(ATP酶)活性的影响。在相同条件(0.4毫摩尔游离镁离子,15微摩尔游离钙离子)下评估的草酸盐支持的钙离子转运,在对照心脏和顿抑心脏中分别从495±29降至395±27纳摩尔钙离子·毫克蛋白-1·分钟-1,表明酶功能存在缺陷。这种缺陷通过最大钙依赖性镁离子ATP酶活性的降低得到证实。将游离[Mg2+]增加以模拟再灌注后的条件导致SR镁离子ATP酶对钙离子的敏感性降低。50%激活从0.6毫摩尔游离[Mg2+]时的对照游离[Ca2+] 0.42微摩尔转变为1.2毫摩尔游离[Mg2+]时的0.63微摩尔游离[Ca2+],这些条件模拟了再灌注后的顿抑心肌。这些结果表明,顿抑后在相似孵育条件下观察到的SR钙离子转运下降,可能会因游离[Mg2+]的持续增加而进一步受到损害。(摘要截断于250字)