首页> 美国卫生研究院文献>The Journal of Physiology >Valinomycin and excitation-contraction coupling in skeletal muscle fibres of the frog.
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Valinomycin and excitation-contraction coupling in skeletal muscle fibres of the frog.

机译:缬草霉素和青蛙骨骼肌纤维中的兴奋-收缩偶联。

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摘要

1. Experiments were carried out on intact frog skeletal muscle fibres to study the role of H+ and K+ as counter-ions during the release of Ca2+ from the sarcoplasmic reticulum (SR). A specific focus was to test whether valinomycin, a potassium ionophore, markedly reduces or abolishes H+ counter-ions fluxes across the SR membrane in response to electrical stimulation. 2. Single twitch fibres, mounted on an optical bench apparatus and stretch to long sarcomere length (3.6-4.0 microns), were activated by single action potentials (16 degrees C). Two optical signals related to excitation-contraction coupling were measured: (i) the 'second component' of the intrinsic birefringence signal, which is closely related to the myoplasmic free [Ca2+] transient, and (ii) the transient myoplasmic alkalization (delta pH) detectable from the pH indicator Phenol Red, a signal thought to reflect the movement of protons from the myoplasm into the SR in partial electrical exchange for released Ca2+. 3. Exposure of a fibre to 5 microM-valinomycin produced a slight, progressive decrease in the amplitude of the birefringence signal, approximately 5-6% per hour. This result suggests that, if anything, the peak rate at which Ca2+ is released from the sarcoplasmic reticulum is slightly decreased by valinomycin. 4. The amplitude of the Phenol Red delta pH signal, measured after exposure of a fibre to valinomycin for a period of at least 60 min, averaged 0.0020 +/- 0.0002 (+/- S.E.M.); this value is slightly smaller than, but not significantly different from (P greater than 0.05; two-tailed t test) that measured in fibres not exposed to valinomycin (0.0025 +/- 0.0002). This result does not support the idea that valinomycin, but virtue of increasing the flux of K+ into the SR, markedly reduces the flux of protons during Ca2+ release. 5. Our findings of minimal changes in the birefringence and delta pH signals are consistent with the idea that, at the time of Ca2+ release, the potassium conductance of the SR membrane is large and not substantially increased by the addition of valinomycin to Ringer solution.
机译:1.对完整的青蛙骨骼肌纤维进行了实验,研究了H +和K +在肌浆网(SR)释放Ca2 +期间作为抗衡离子的作用。一个特别的重点是测试缬胺霉素(一种钾离子载体)是否响应电刺激而显着降低或消除了跨SR膜的H +抗衡离子通量。 2.通过单动作电位(16℃)激活安装在光具座装置上并拉伸至长肌节长度(3.6-4.0微米)的单抽动纤维。测量了与激发-收缩耦合有关的两个光信号:(i)本征双折射信号的“第二分量”,与肌质游离[Ca2 +]瞬变密切相关;(ii)瞬态肌质碱化(δpH) )可以从pH指示剂酚红中检测到,该信号被认为反映了质子从肌质到SR的运动,其中部分电交换了释放的Ca2 +。 3.将纤维暴露于5 microM缬氨酸霉素会使双折射信号的幅度逐渐减小,约为每小时5-6%。这个结果表明,如果有的话,缬氨霉素会稍微降低从肌浆网释放Ca 2+的峰值速率。 4.在纤维暴露于缬霉素中至少60分钟后测得的酚红δpH信号的幅度平均为0.0020 +/- 0.0002(+/- S.E.M。);该值比未暴露于缬氨霉素的纤维中测得的值略小,但无显着差异(P大于0.05;两尾t检验)(0.0025 +/- 0.0002)。该结果不支持缬氨霉素,而是由于增加了K +进入SR的通量,从而显着降低了Ca2 +释放过程中质子的通量。 5.我们对双折射和pH值信号的最小变化的发现与以下想法是一致的,即在Ca2 +释放时,SR膜的钾电导率很大,并且通过向Ringer溶液中添加缬氨菌素不会显着增加钾电导率。

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