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青蛙骨骼肌膜的电压传感器在兴奋-收缩偶联过程中发挥作用需要钙。

Voltage sensors of the frog skeletal muscle membrane require calcium to function in excitation-contraction coupling.

作者信息

Brum G, Fitts R, Pizarro G, Ríos E

机构信息

Department of Physiology, Rush University, School of Medicine, Chicago, IL 60612.

出版信息

J Physiol. 1988 Apr;398:475-505. doi: 10.1113/jphysiol.1988.sp017053.

Abstract
  1. Intramembrane charge movements and changes in intracellular Ca2+ concentration (Ca2+ transients) elicited by pulse depolarization were measured in frog fast twitch cut muscle fibres under voltage clamp. 2. Extracellular solutions with very low [Ca2+] and 2 mM-Mg2+ , shown in the previous paper to reduce Ca2+ release from the sarcoplasmic reticulum (SR), were found to cause two changes in charge movement: (a) a decrease (-12 nC/microF) in the charge that moves during depolarizing pulses from -90 to 0 mV, termed here 'charge 1'; (b) an increase (+7 nC/microF) in the charge moved by hyperpolarizing pulses from -90 to -180 mV, termed 'charge 2'. 3. The increase in charge moved by hyperpolarizing pulses was correlated (r = 0.64) with the decrease in charge moved by depolarizing pulses and both were correlated with the inhibition of Ca2+ release recorded in the same fibres. 4. The low Ca2+ solutions caused a shift to more negative voltages of the dependence relating charge movement and holding potential (VH). This shift is of similar magnitude (about 22 mV) and direction as the shift in the curve relating Ca2+ release flux to VH (previous paper). 5. In solutions with normal [Ca2+] a conditioning depolarization to 0 mV, of 2 s duration, placed 100 ms before a test pulse from -70 to 0 mV, reduced by 30% the amount of charge displaced by the test pulse. Conditioning pulses of 1 s or less caused potentiation of charge movement by up to 30%. 6. In low Ca2+ solutions, reduction of charge was observed at all durations of the conditioning pulse. The duration for half-inhibition was near 200 ms. 7. An extracellular solution with no metal cations caused a more radical inhibition than the low Ca2+ solutions that contained Mg2+. The inhibition of Ca2+ release was essentially complete (90-100%). The charge moved by a pulse to 0 mV was reduced by 20 nC/microF and the charge moved by a pulse to -170 mV increased 8 nC/microF. This shows that Mg2+ supports excitation-contraction (E-C) coupling to some extent. 8. A state model of the voltage sensor of E-C coupling explains qualitatively the observations in both papers.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在电压钳制下,对青蛙快肌离体肌纤维施加脉冲去极化,测量膜内电荷移动以及由此引发的细胞内钙离子浓度变化(钙离子瞬变)。2. 此前论文表明,极低钙离子浓度([Ca2+])和2 mM 镁离子的细胞外溶液可减少肌浆网(SR)释放钙离子。研究发现,这种溶液会引起电荷移动的两种变化:(a)在从 -90 mV 去极化至 0 mV 的脉冲期间移动的电荷量减少(-12 nC/微法),此处称为“电荷1”;(b)在从 -90 mV 超极化至 -180 mV 的脉冲期间移动的电荷量增加(+7 nC/微法),称为“电荷2”。3. 超极化脉冲移动的电荷量增加与去极化脉冲移动的电荷量减少相关(r = 0.64),且二者均与同一纤维中记录到的钙离子释放受抑制情况相关。4. 低钙离子溶液导致电荷移动与钳制电位(VH)之间的依赖关系向更负的电压偏移。这种偏移的幅度(约22 mV)和方向与钙离子释放通量与VH之间曲线的偏移相似(此前论文)。5. 在正常[Ca2+]溶液中,在从 -70 mV 至 0 mV 的测试脉冲前100 ms施加持续2 s、幅度为0 mV的预处理去极化,可使测试脉冲移动的电荷量减少30%。持续1 s或更短时间的预处理脉冲可使电荷移动增强高达3

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