Duke A M, Steele D S
Department of Biology, University of Leeds, Leeds LS2 9JT, UK.
Pflugers Arch. 1998 Jun;436(1):104-11. doi: 10.1007/s004240050610.
The effects of the sarcoplasmic reticulum (SR) Ca2+ pump inhibitor cyclopiazonic acid (CPA) were studied in saponin-permeabilized frog skeletal muscle fibres. Release of Ca2+ from the SR was triggered by brief (2 s) applications of 40 mM caffeine at 2-min intervals. Changes in [Ca2+] within the fibre were monitored continuously using Fura-2 fluorescence. At a bathing [Ca2+] of 100 nM, introduction of 20 microM CPA induced a slow release of Ca2+ from the SR. The following one to two caffeine-induced Ca2+ transients were markedly increased in amplitude and duration. Thereafter, the caffeine-induced Ca2+ transients decreased progressively and were barely detectable 6-7 min after introduction of CPA. However, increasing the bathing [Ca2+] or increasing the Ca2+ loading period resulted in a partial recovery of the caffeine-induced Ca2+ transients, suggesting that pump inhibition is incomplete, even in the presence of 100 microM CPA. The slow Ca2+ efflux induced by CPA was insensitive to ryanodine, but absent following abolition of SR Ca2+ pump activity by ATP withdrawal. These results suggest that the caffeine-induced Ca2+ transient reflects a balance between efflux via the SR Ca2+ channel and reuptake by the Ca pump. Ca2+ release upon addition of CPA may result from inhibition of SR Ca2+ uptake, which reveals a tonic Ca2+ efflux that is independent of the Ca2+ release channels.
在皂素通透的青蛙骨骼肌纤维中研究了肌浆网(SR)Ca2+泵抑制剂环匹阿尼酸(CPA)的作用。每隔2分钟短暂(2秒)施加40 mM咖啡因,触发SR中Ca2+的释放。使用Fura-2荧光连续监测纤维内[Ca2+]的变化。在100 nM的浴液[Ca2+]条件下,加入20 μM CPA会诱导SR缓慢释放Ca2+。随后一到两个咖啡因诱导的Ca2+瞬变在幅度和持续时间上显著增加。此后,咖啡因诱导的Ca2+瞬变逐渐减少,在加入CPA后6 - 7分钟几乎检测不到。然而,增加浴液[Ca2+]或延长Ca2+加载时间会导致咖啡因诱导的Ca2+瞬变部分恢复,这表明即使存在100 μM CPA,泵抑制也不完全。CPA诱导的缓慢Ca2+外流对兰尼碱不敏感,但在通过去除ATP消除SR Ca2+泵活性后则不存在。这些结果表明,咖啡因诱导的Ca2+瞬变反映了通过SR Ca2+通道的外流与Ca泵再摄取之间的平衡。加入CPA后Ca2+释放可能是由于SR Ca2+摄取受到抑制,这揭示了一种与Ca2+释放通道无关的持续性Ca2+外流。