Krause S M, Rozanski D
Department of Physiology, Jefferson Medical College, Philadelphia, Pa.
Circulation. 1991 Sep;84(3):1378-83. doi: 10.1161/01.cir.84.3.1378.
Myocardial stunning has been associated with a greater than twofold increase in intracellular free [Mg2+] from 0.6 to 1.5 mM. The effect of this increase in free [Mg2+] on the function of the sarcoplasmic reticulum (SR) Ca2+ pump was assessed in SR isolated from Langendorff perfused, isovolumic rabbit hearts after 15 minutes of global ischemia.
Our results indicate that myocardial stunning results in a shift in the Ca2+ sensitivity of oxalate-supported, Ca2+ transport over the entire range of free [Ca2+] associated with the cardiac cycle. Using 0.6 mM free Mg2+ as control, maximal rates of Ca2+ transport occurred at 1 microM free Ca2+ (control, 519 +/- 32; stunned, 337 +/- 37 nmol Ca2+.min-1.mg-1). At 0.56 microM free Ca2+, SR Ca2+ transport was reduced from a control of 351 +/- 49 to 263 +/- 12 nmol Ca2+.min-1.mg-1 at 0.6 mM free [Mg2+]. Moreover, an increase in the free [Mg2+] from 0.6 to 1.5 mM results in a greater shift in the Ca2+ activation curve with no change in the level of maximal activation. Ca2+ transport at 0.56 microM free Ca2+ was shifted in the stunned SR from 263 +/- 12 to 138 +/- 29 nmol Ca2+.min-1.mg-1 at 0.6 and 1.5 mM free Mg2+, respectively.
These results indicate that an increase in free [Mg2+] after stunning in combination with the inherent defect in the SR Ca2+ ATPase may reduce the ability of the cell to regulate Ca2+ to a greater extent than previously observed. This impairment in Ca2+ regulatory function may contribute directly to the increase in diastolic tone and indirectly to the reduced systolic function characteristic of the stunned myocardium.
心肌顿抑与细胞内游离[Mg2+]从0.6 mM增加至1.5 mM以上两倍多有关。在全心缺血15分钟后,从Langendorff灌注的等容兔心脏分离的肌浆网(SR)中,评估了游离[Mg2+]的这种增加对SR Ca2+泵功能的影响。
我们的结果表明,心肌顿抑导致在与心动周期相关的整个游离[Ca2+]范围内,草酸盐支持的Ca2+转运的Ca2+敏感性发生改变。以0.6 mM游离Mg2+作为对照,Ca2+转运的最大速率出现在1 microM游离Ca2+时(对照,519±32;顿抑,337±37 nmol Ca2+·min-1·mg-1)。在0.56 microM游离Ca2+时,在0.6 mM游离[Mg2+]条件下,SR Ca2+转运从对照的351±49降至263±12 nmol Ca2+·min-1·mg-1。此外,游离[Mg2+]从0.6 mM增加至1.5 mM导致Ca2+激活曲线有更大的改变,而最大激活水平无变化。在0.6 mM和1.5 mM游离Mg2+条件下,在顿抑的SR中,0.56 microM游离Ca2+时的Ca2+转运分别从263±12降至138±29 nmol Ca2+·min-1·mg-1。
这些结果表明,顿抑后游离[Mg2+]的增加与SR Ca2+ ATP酶的内在缺陷相结合,可能比以前观察到的情况更大程度地降低细胞调节Ca2+的能力。Ca2+调节功能的这种损害可能直接导致舒张期张力增加,并间接导致顿抑心肌收缩功能降低的特征。