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豚鼠经N-溴乙酰胺处理的心肌细胞中指数型钠离子电流激活的定量分析。

Quantification of exponential Na+ current activation in N-bromoacetamide-treated cardiac myocytes of guinea-pig.

作者信息

Mitsuiye T, Noma A

机构信息

Department of Physiology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

J Physiol. 1993 Jun;465:245-63. doi: 10.1113/jphysiol.1993.sp019675.

Abstract
  1. The activation kinetics of the Na+ current was investigated in single ventricular cells of the guinea-pig heart using an improved oil-gap voltage clamp method. The inactivation of the current was removed by an intracellular application of N-bromoacetamide (NBA) for less than 1 min. Although the NBA treatment slightly decreased the peak amplitudes (81.7 +/- 13.4% of control, n = 15), the Na+ current remained stable after the removal of inactivation. 2. On depolarization, the activation of Na+ current took an exponential time course after the capacitive current decreased to 5% of its peak amplitude (40-100 microseconds after the pulse onset). The time course of deactivation, recorded on repolarization from 1.2 ms depolarization, was also a single exponential. 3. The time constants of activation and deactivation were almost identical when compared at a given test potential within a range of -50 to -30 mV. These findings indicate that the cardiac Na+ current activation is determined by m1 kinetics, or one rate-limiting step. 4. At potentials negative to -60 mV, the deactivation was complete, and its time constant decreased e-fold per 20.3 +/- 1.8 mV hyperpolarization (n = 7). 5. The degree of steady-state activation (m(infinity)) was fitted to a Boltzmann equation with a slope factor of 7.4 +/- 0.3 mV and a half-maximum potential of -33.3 +/- 0.8 mV (n = 8). 6. Rate constants for the rate-limiting activation step between a closed state and an open state (alpha m, beta m), were determined from m(infinity) and tau m over a potential range between -100 and +50 mV. On a logarithmic scale, beta m-1 was a linear function of the membrane potential over the range -100 and -30 mV. 7. Fitting the newly determined activation kinetics to the rising phase of the action potential indicated that the activation kinetics in the present study is relevant to the physiological action potential. The density of the Na+ channels thus obtained was 1075 +/- 186 pF-1 (n = 6). 8. The measurements in the NBA-treated Na+ current were compared with those obtained without treatment.
摘要
  1. 采用改良的油隙电压钳法,在豚鼠心脏单个心室细胞中研究了Na⁺电流的激活动力学。通过细胞内应用N - 溴乙酰胺(NBA)不到1分钟来消除电流的失活。尽管NBA处理使峰值幅度略有降低(为对照的81.7±13.4%,n = 15),但消除失活后Na⁺电流仍保持稳定。2. 去极化时,在电容性电流降至其峰值幅度的5%后(脉冲开始后40 - 100微秒),Na⁺电流的激活呈指数时间进程。从1.2毫秒去极化复极化时记录的失活时间进程也是单指数的。3. 在 - 50至 - 30 mV范围内的给定测试电位下比较时,激活和失活的时间常数几乎相同。这些发现表明心脏Na⁺电流激活由m1动力学或一个限速步骤决定。4. 在负于 - 60 mV的电位下,失活完成,其时间常数每超极化20.3±1.8 mV下降一个e倍(n = 7)。5. 稳态激活程度(m(∞))拟合到玻尔兹曼方程,斜率因子为7.4±0.3 mV,半最大电位为 - 33.3±0.8 mV(n = 8)。6. 从 - 100至 + 50 mV的电位范围内的m(∞)和τm确定了从关闭状态到开放状态的限速激活步骤的速率常数(αm,βm)。在对数尺度上,βm⁻¹在 - 100至 - 30 mV范围内是膜电位的线性函数。7. 将新确定的激活动力学拟合到动作电位的上升相表明本研究中的激活动力学与生理动作电位相关。由此获得的Na⁺通道密度为1075±186 pF⁻¹(n = 6)。8. 将NBA处理的Na⁺电流的测量结果与未处理时获得的结果进行比较。

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Unitary sodium channels in isolated cardiac myocytes of rabbit.
Circ Res. 1983 Dec;53(6):823-9. doi: 10.1161/01.res.53.6.823.
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Sodium channels in cultured cardiac cells.培养心肌细胞中的钠通道。
J Physiol. 1983 Jul;340:389-401. doi: 10.1113/jphysiol.1983.sp014768.

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