首页> 外文期刊>The Journal of Physiology >Voltage-dependent Ca2+ release from the SR of feline ventricular myocytes is explained by Ca2+-induced Ca2+ release.
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Voltage-dependent Ca2+ release from the SR of feline ventricular myocytes is explained by Ca2+-induced Ca2+ release.

机译:从猫心室肌细胞的SR电压依赖性Ca2 +释放可以通过Ca2 +诱导的Ca2 +释放来解释。

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摘要

1. Direct voltage-gated (voltage-dependent Ca2+ release, VDCR) and Ca2+ influx-gated (Ca2+-induced Ca2+ release, CICR) sarcoplasmic reticulum (SR) Ca2+ release were studied in feline ventricular myocytes. The voltage-contraction relationship predicted by the VDCR hypothesis is sigmoidal with large contractions at potentials near the Ca2+ equilibrium potential (ECa). The relationship predicted by the CICR hypothesis is bell-shaped with no contraction at ECa. 2. The voltage dependence of contraction was measured in ventricular myocytes at physiological temperature (37 C), resting membrane potential and physiological [K+]. Experiments were performed with cyclic adenosine 3',5'-monophosphate (cAMP) in the pipette or in the presence of the beta-adrenergic agonist isoproterenol (isoprenaline; ISO). 3. The voltage-contraction relationship was bell-shaped in Na+-free solutions (to eliminate the Na+ current and Na+-Ca2+ exchange, NCX) but the relationship was broader than the L-type Ca2+ current (ICa,L)-voltage relationship. 4. Contractions induced with voltage steps from normal resting potentials to -40 mV are thought to represent VDCR rather than CICR. We found that cAMP and ISO shifted the voltage dependence of ICa,L activation to more negative potentials so that ICa,L was always present with steps to -40 mV. ICa,L at -40 mV inactivated when the holding potential was decreased (VL = -57.8 +/- 0.49 mV). 5. ISO increased inward current, SR Ca2+ load and contraction in physiological [Na+] and a broad bell-shaped voltage-contraction relationship was observed. Inhibition of reverse-mode NCX, decreasing ICa,L and decreasing SR Ca2+ loading all decreased contractions at strongly positive potentials near ECa. 6. The voltage-contraction relationship in 200 &mgr;M cadmium (Cd2+) was bell-shaped, supporting a role of ICa,L rather than VDCR. 7. All results could be accounted for by the CICR hypothesis, and many results exclude the VDCR hypothesis.
机译:1.研究了猫心室肌细胞中直接电压门控(电压依赖性Ca2 +释放,VDCR)和Ca2 +流入门控(Ca2 +诱导的Ca2 +释放,CICR)肌浆网(SR)Ca2 +的释放。 VDCR假设所预测的电压-收缩关系为S型,在Ca2 +平衡电势(ECa)附近的电势下具有大的收缩。由CICR假设预测的关系是钟形的,在ECa处没有收缩。 2.在生理温度(37℃),静息膜电位和生理[K +]下测量心室肌细胞收缩的电压依赖性。在移液管中或在β-肾上腺素能激动剂异丙肾上腺素(异丙肾上腺素; ISO)存在下,用环状3',5'-单磷酸腺苷(cAMP)进行实验。 3.在无Na +的溶液中,电压收缩关系呈钟形(以消除Na +电流和Na + -Ca2 +交换,NCX),但该关系比L型Ca2 +电流(ICa,L)-电压关系宽。 。 4.从正常静息电位到-40 mV的电压阶跃引起的收缩被认为代表VDCR而不是CICR。我们发现cAMP和ISO将ICa,L激活的电压依赖性转移到更多的负电势,因此ICa,L始终以-40 mV的步长存在。当保持电位降低(VL = -57.8 +/- 0.49 mV)时,-40 mV的ICa,L失活。 5. ISO增加了生理学[Na +]中的内向电流,SR Ca2 +负载和收缩,并且观察到了宽的钟形电压收缩关系。反向模式NCX的抑制,ICa,L的降低和SR Ca2 +负载的降低均在ECa附近的强正电势下减少了收缩。 6. 200 mg C(Cd2 +)中的电压-收缩关系呈钟形,支持ICa,L而不是VDCR。 7.所有结果都可以由CICR假设解释,许多结果不包括VDCR假设。

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