Allen D G, Orchard C H
J Physiol. 1983 Jun;339:107-22. doi: 10.1113/jphysiol.1983.sp014706.
Papillary muscles from rats, cats and ferrets were microinjected with aequorin, a photoprotein which emits light as a function of Ca2+ concentration. The effects of hypoxia and different types of metabolic inhibition on intracellular Ca2+ concentration ([ Ca2+]i) and tension were studied. 2. Exposure of the muscle to hypoxia (PO2 less than 5 mmHg) or CN- caused a reversible decrease in developed tension, with no change in the magnitude of the Ca transient associated with each contraction. The rate of decline of the Ca transient was decreased slightly but significantly during these interventions. 3. In half the preparations examined, the initial fall in tension produced by hypoxia was interrupted by a short-lived increase in developed tension. No change in the Ca transient was associated with this increase in tension. 4. After exposure of papillary muscles to glucose-free Tyrode solution for short periods (less than 1 hr), hypoxia and CN- had a similar effect on the magnitude of the light transient and developed tension to section 2 above. After perfusion with glucose-free Tyrode solution for longer periods (greater than 2 hr), hypoxia and CN- caused a greater decrease in developed tension and a marked decrease in the magnitude of the Ca transient. 5. The addition of CN- to papillary muscles which were superfused with Tyrode solution containing 2-deoxyglucose instead of glucose, caused a rapid decrease in the magnitude of the Ca transient and of developed tension. These changes were not fully reversible. 6. In muscles which developed an hypoxic contracture, the resting [Ca2+]i did not rise by more than a factor of 1.4. 7. It is concluded that when glycolysis can proceed, inhibition of oxidative phosphorylation results in a decrease in developed tension with no change in the magnitude of the Ca transient. This decrease in the apparent sensitivity of the contractile proteins to Ca2+ is attributable to the decrease in intracellular pH known to occur in this situation. There may also be a second mechanism tending to reduce the Ca transient under these conditions. 8. During inhibition of glycolysis and oxidative phosphorylation, developed tension falls as a result of decreased Ca transients. This could be because the free energy of hydrolysis of ATP falls below the level required to pump Ca from the myoplasm to the sarcoplasmic reticulum.
将水母发光蛋白(一种根据钙离子浓度发光的光蛋白)微量注射到大鼠、猫和雪貂的乳头肌中。研究了缺氧和不同类型的代谢抑制对细胞内钙离子浓度([Ca2+]i)和张力的影响。2. 将肌肉暴露于缺氧环境(氧分压低于5 mmHg)或氰化物中会导致已产生的张力可逆性降低,每次收缩相关的钙瞬变幅度没有变化。在这些干预过程中,钙瞬变的下降速率略有但显著降低。3. 在一半的受试制剂中,缺氧引起的张力最初下降被已产生张力的短暂增加打断。这种张力增加与钙瞬变没有变化相关。4. 将乳头肌短时间(少于1小时)暴露于无葡萄糖的台氏液后,缺氧和氰化物对光瞬变幅度和已产生张力的影响与上述第2部分相似。用无葡萄糖的台氏液灌注较长时间(大于2小时)后,缺氧和氰化物导致已产生的张力下降更大,钙瞬变幅度显著降低。5. 向用含2 - 脱氧葡萄糖而非葡萄糖的台氏液灌流的乳头肌中添加氰化物,会导致钙瞬变幅度和已产生张力迅速降低。这些变化并非完全可逆。6. 在出现缺氧性挛缩的肌肉中,静息[Ca2+]i升高不超过1.4倍。7. 得出的结论是,当糖酵解能够进行时,氧化磷酸化的抑制会导致已产生的张力降低,而钙瞬变幅度没有变化。收缩蛋白对钙离子表观敏感性的这种降低归因于已知在这种情况下发生的细胞内pH值降低。在这些条件下可能还存在第二种倾向于减少钙瞬变的机制。8. 在糖酵解和氧化磷酸化受到抑制期间,由于钙瞬变减少,已产生的张力下降。这可能是因为ATP水解的自由能降至将钙离子从肌浆泵入肌浆网所需水平以下。