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雷诺丁和丁卡因对青蛙骨骼肌电荷移动和钙瞬变的不同影响。

Differential effects of ryanodine and tetracaine on charge movement and calcium transients in frog skeletal muscle.

作者信息

García J, Avila-Sakar A J, Stefani E

机构信息

Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030.

出版信息

J Physiol. 1991;440:403-17. doi: 10.1113/jphysiol.1991.sp018715.

Abstract
  1. Charge movement and myoplasmic calcium transients were simultaneously recorded from frog skeletal muscle fibres by using the double-seal Vaseline-gap technique. Calcium transients were monitored with the fluorescent indicator Rhod-2. 2. Ryanodine modified the kinetics and the total amount of charge moved during depolarizing pulses (Q(on)), while it did not significantly modify the charge after repolarization (Q(off)). The extracellular application of 100 microM-ryanodine elicited a temporary initial increase of the delayed component of charge movement (Q gamma) and the calcium transient. Both phenomena were later blocked with the same temporal course and to the same extent. 3. The blockade of Q gamma and the calcium transient was also observed with ryanodine concentrations of 1-10 microM. For membrane potentials positive to -10mV, the Qon measured was larger in the presence of ryanodine; Qoff was not modified. 4. Tetracaine (400-500 microM) blocked a similar delayed component of Qon, identified as Q gamma, as well as the calcium transient monitored simultaneously. This effect was observed in the first minutes after the addition of tetracaine to the extracellular solution. 5. Tetracaine blocked a faster initial component of Qon for voltages positive to -10 mV, corresponding to the voltage range of activation of the calcium current. At these same membrane potentials, Qoff was also reduced to a similar extent to Qon. 6. Ryanodine and tetracaine showed different effects on calcium current. Whereas the slow calcium current was not modified upon the addition of ryanodine, it was completely blocked in the presence of tetracaine. The blockade of the slow calcium current made evident the fast calcium current. The effects of tetracaine on the charge movement, the calcium transient and the slow calcium current were reversible. 7. These results suggest that ryanodine and tetracaine may act at different sites. Ryanodine exerts its effect on the sarcoplasmic reticulum ryanodine receptor, blocking calcium release and Q gamma, while tetracaine at these concentrations may affect the release channel and the dihydropyridine receptor, causing a blockade of the charge movement, calcium transient and calcium current.
摘要
  1. 采用双封接凡士林间隙技术,同时记录青蛙骨骼肌纤维的电荷移动和肌浆钙瞬变。用荧光指示剂Rhod-2监测钙瞬变。2. 雷诺丁改变了去极化脉冲期间移动的电荷动力学和总量(Q(on)),而对复极化后的电荷(Q(off))没有显著影响。细胞外施加100 microM的雷诺丁会引起电荷移动延迟成分(Qγ)和钙瞬变的暂时初始增加。两种现象随后以相同的时间进程和相同程度被阻断。3. 当雷诺丁浓度为1 - 10 microM时,也观察到Qγ和钙瞬变的阻断。对于膜电位正向至 -10mV,在存在雷诺丁的情况下测得的Qon更大;Qoff未改变。4. 丁卡因(400 - 500 microM)阻断了Qon中类似的延迟成分,确定为Qγ,以及同时监测的钙瞬变。在将丁卡因添加到细胞外溶液后的最初几分钟内观察到这种效应。5. 对于正向至 -10 mV的电压,丁卡因阻断了Qon中更快的初始成分,这对应于钙电流激活的电压范围。在这些相同的膜电位下,Qoff也降低到与Qon相似的程度。6. 雷诺丁和丁卡因对钙电流表现出不同的影响。加入雷诺丁后慢钙电流未改变,而在存在丁卡因的情况下它被完全阻断。慢钙电流的阻断使快钙电流显现出来。丁卡因对电荷移动、钙瞬变和慢钙电流的影响是可逆的。7. 这些结果表明,雷诺丁和丁卡因可能作用于不同位点。雷诺丁对肌浆网雷诺丁受体发挥作用,阻断钙释放和Qγ,而这些浓度的丁卡因可能影响释放通道和二氢吡啶受体,导致电荷移动、钙瞬变和钙电流的阻断。

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