Luciani G B, D'Agnolo A, Mazzucco A, Gallucci V, Salviati G
Department of Cardiovascular Surgery, University of Verona, Italy.
Am J Physiol. 1993 Oct;265(4 Pt 2):H1334-41. doi: 10.1152/ajpheart.1993.265.4.H1334.
The effects of global ischemia on the contractile system and on sarcoplasmic reticulum (SR) function were studied by measuring the isometric tension and the SR Ca2+ release activity of chemically skinned cardiac fiber preparations from seven patients undergoing open-heart surgery. Ten minutes of ischemia caused 1) a decrease in the myofilament sensitivity to Ca2+ (expected Ca2+ concentration giving half-maximal tension; from 0.69 +/- 0.04 to 1.38 +/- 0.06 microM, n = 7) and in the cooperativity index (Hill coefficient; from 2.61 +/- 0.45 to 0.92 +/- 0.15, n = 7), 2) a decrease in myosin light chain phosphorylation, and 3) a 300% increase in the threshold caffeine concentration for SR Ca2+ efflux channel activation, with a 30% reduction in the rate of Ca2+ release by caffeine at threshold concentrations and a 23% reduction in the rate of release by 20 mM caffeine. After preincubation with 5 microM trifluoperazine, a calmodulin antagonist, the caffeine threshold of ischemic and control cardiac muscle became comparable. Most changes were reversed by reperfusion, while the caffeine threshold was still two times greater than control. These results indicate that ischemia caused alterations of the cardiac muscle contractile apparatus and the SR that were reversed only after reperfusion.
通过测量7例接受心脏直视手术患者化学去表皮心肌纤维制剂的等长张力和肌浆网(SR)Ca2+释放活性,研究了整体缺血对收缩系统和肌浆网功能的影响。缺血10分钟导致:1)肌丝对Ca2+的敏感性降低(产生半数最大张力时的预期Ca2+浓度;从0.69±0.04降至1.38±0.06微摩尔,n = 7)以及协同指数(希尔系数;从2.61±0.45降至0.92±0.15,n = 7),2)肌球蛋白轻链磷酸化降低,3)SR Ca2+外流通道激活的咖啡因阈值增加300%,在阈值浓度下咖啡因引起的Ca2+释放速率降低30%,20 mM咖啡因引起的释放速率降低23%。用钙调蛋白拮抗剂5微摩尔三氟拉嗪预孵育后,缺血和对照心肌的咖啡因阈值变得相当。大多数变化在再灌注后逆转,而咖啡因阈值仍比对照高两倍。这些结果表明,缺血导致心肌收缩装置和肌浆网发生改变,这些改变仅在再灌注后才逆转。