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在兔心肌细胞咖啡因挛缩过程中,线粒体和肌膜的Ca2+转运降低细胞内Ca2+浓度([Ca2+]i) 。

Mitochondrial and sarcolemmal Ca2+ transport reduce [Ca2+]i during caffeine contractures in rabbit cardiac myocytes.

作者信息

Bassani R A, Bassani J W, Bers D M

机构信息

Division of Biomedical Sciences, University of California, Riverside 92521.

出版信息

J Physiol. 1992;453:591-608. doi: 10.1113/jphysiol.1992.sp019246.

Abstract
  1. Contraction and intracellular Ca2+ (Ca2+i) transients were measured in isolated rabbit ventricular myocytes during twitches and contractures induced by rapid application of 10 mM-caffeine. 2. The amplitude of caffeine-induced contractures and the accompanying Ca2+i transients were larger than during normal twitches and also declined more slowly. This may be because only a fraction of sarcoplasmic reticulum (SR) Ca2+ is released during a normal twitch, or because of a temporal overlap of SR Ca2+ release and uptake during the twitch. 3. When a caffeine contracture was initiated in Na(+)-free, Ca(2+)-free medium (to prevent sarcolemmal Na(+)-Ca2+ exchange) the contracture and Ca2+i transient were larger and decreased much more slowly. Thus, Ca2+ extrusion via Na(+)-Ca2+ exchange may limit the amplitude of caffeine-induced contractures. 4. Relaxation half-time (t1/2) for the twitch (0.17 +/- 0.03 s) was increased to 0.54 +/- 0.07 s for caffeine contractures in control solution and 8.8 +/- 1 s for caffeine-induced contractures in Na(+)-free, Ca(2+)-free solution. These results confirm that the SR Ca2+ pump and Na(+)-Ca2+ exchange are the predominant mechanisms for cytoplasmic Ca2+ removal during relaxation. However slower mechanisms can still reduce intracellular [Ca2+]. 5. Relaxation of caffeine contractures in Na(+)-free solution was further slowed when (a) mitochondrial Ca2+ uptake was inhibited with the oxidative phosphorylation uncoupler, FCCP (t1/2 = 19.7 +/- 3.2 s), or (b) the sarcolemmal Ca(2+)-ATPase pumping ability was depressed by a large transmembrane [Ca2+] gradient (t1/2 = 27.5 +/- 6.9 s). 6. When the four Ca2+ transport systems were simultaneously inhibited (i.e. SR Ca2+ pump, Na(+)-Ca2+ exchange, mitochondrial Ca2+ uptake and sarcolemmal Ca2+ pump), relaxation was practically abolished, but the cell could recover quickly when Na+ was reintroduced and caffeine removed. 7. We conclude that, under our experimental conditions, the sarcolemmal Ca2+ pump and mitochondria are approximately 37- and 50-fold slower than the Na(+)-Ca2+ exchange at removing Ca2+ from the cytoplasm. Additionally, the SR Ca2+ pump is about 3-4 times faster than Na(+)-Ca2+ exchange.
摘要
  1. 在快速施加10 mM咖啡因诱导的单收缩和挛缩过程中,对分离的兔心室肌细胞的收缩和细胞内Ca2+(Ca2+i)瞬变进行了测量。2. 咖啡因诱导的挛缩幅度以及伴随的Ca2+i瞬变大于正常单收缩期间,且下降也更缓慢。这可能是因为在正常单收缩期间只有一部分肌浆网(SR)Ca2+被释放,或者是因为在单收缩期间SR Ca2+释放和摄取存在时间重叠。3. 当在无Na+、无Ca2+的培养基中引发咖啡因挛缩时(以防止肌膜Na+-Ca2+交换),挛缩和Ca2+i瞬变更大且下降更缓慢得多。因此,通过Na+-Ca2+交换的Ca2+外流可能会限制咖啡因诱导的挛缩幅度。4. 单收缩的舒张半衰期(t1/2)(0.17±0.03秒)在对照溶液中对于咖啡因挛缩增加到0.54±0.07秒,在无Na+、无Ca2+溶液中对于咖啡因诱导的挛缩增加到8.8±1秒。这些结果证实,SR Ca2+泵和Na+-Ca2+交换是舒张期间细胞质Ca2+清除的主要机制。然而,较慢的机制仍然可以降低细胞内[Ca2+]。5. 当(a)用氧化磷酸化解偶联剂FCCP抑制线粒体Ca2+摄取时(t1/2 = 19.7±3.2秒),或(b)大的跨膜[Ca2+]梯度降低肌膜Ca2+-ATP酶的泵送能力时(t1/2 = 27.5±6.9秒),无Na+溶液中咖啡因挛缩的舒张进一步减慢。6. 当四个Ca2+转运系统同时被抑制时(即SR Ca2+泵、Na+-Ca2+交换、线粒体Ca2+摄取和肌膜Ca2+泵),舒张实际上被消除,但当重新引入Na+并去除咖啡因时细胞可以快速恢复。7. 我们得出结论,在我们的实验条件下,肌膜Ca2+泵和线粒体在从细胞质中清除Ca2+方面比Na+-Ca2+交换慢约37倍和50倍。此外,SR Ca2+泵比Na+-Ca2+交换快约3 - 4倍。

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