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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Voltage-operated potassium currents in the somatic membrane of rat dorsal root ganglion neurons: ontogenetic aspects.
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Voltage-operated potassium currents in the somatic membrane of rat dorsal root ganglion neurons: ontogenetic aspects.

机译:大鼠背根神经节神经元体细胞膜中的电压操作钾电流:遗传方面。

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Whole-cell transmembrane potassium currents were studied in somatic membrane of freshly isolated rat dorsal root ganglion neurons. We defined three types of potassium currents, which were separated on the basis of their different potential dependence of activation and sensitivity to external tetraethylammonium and 4-aminopyridine. The potential dependence of kinetic and steady-state properties of a fast inactivating potassium current, a slow inactivating potassium current and a non-inactivating delayed rectifier current were described by the Hodgkin-Huxley equations. A transient fast inactivating potassium current was activated at the most negative membrane potentials and was not reduced in the presence of 10 mM tetraethylammonium in the external solution. 4-Aminopyridine (2 mM) caused an 80% inhibition of this current. The activation of the fast inactivating potassium current was properly described by fitting a single exponent raised to the fourth power. The time constant of activation changed from 4 to 1 ms in the voltage range between -30 and +40 mV. The time constant of inactivation decreased from 35 to 15 ms over the same range of potentials. Parameters for the fit of a Boltzmann equation to mean values for steady-state activation were V1/2=-20mV, k=11.8mV, and for steady-state inactivation V1/2= -85 mV, k=-9.8 mV. A transient slow inactivating potassium current had an activation threshold between -40 and -30 mV. At 2 mM 4-aminopyridine, the depression of the slow potassium current was 55%. The extracellular application of 10 mM tetraethylammonium was less effective and evoked a 40% reduction. The activation of the slow inactivating potassium current was also described by a single exponential function raised to the fourth power. The time constant of activation decreased from 12 ms at a membrane potential of -10 mV to 4 ms at the potential of 60 mV. The inactivation of slow inactivating potassium current was described by two exponents. The time constant for the fast exponent ranged from 300 ms at -20 mV to 160 ms at +60 mV. The slower exponent was also potential dependent and its time constant ranged from approximately 2600 to 1600 ms over the same potentials. Parameters for the Boltzmann equation fittings to mean values were V1/2= -12.8 mV, k=13.4 mV and V1/2= -54.6 mV, k= -12 mV for steady-state activation and inactivation, respectively. A non-inactivating delayed rectifier potassium current was activated at the most positive membrane potentials. This non-inactivating current did not change in the presence of 4-aminopyridine. Extracellular tetraethylammonium (10 mM) caused a 70% reduction of this current. The activation of the non-inactivating potassium current was described by one exponent raised to the fourth power. The time constant for activation ranged from 85 ms at -5 mV to 30 ms at 45 mV. No time-dependent inactivation was observed during 15-s testing potentials in the voltage range between 10 and +60 mV. The activation behavior was characterized by V1/2=15.3 mV, k=12.5 mV. The densities of these potassium currents were studied for three groups of animals: one, five to six and 14-15 days of postnatal development. Fifty cells were examined in each age group. All three types of potassium currents were found in each investigated neuron. The mean densities of slow and fast inactivating potassium currents increased during ontogenetic development. The densities of non-inactivating delayed rectifier potassium current decreased in the first week of ontogenetic development and did not change thereafter.
机译:在新鲜分离的大鼠背根神经节神经元的体细胞膜中研究全细胞跨膜钾电流。我们定义了三种钾电流,根据它们对活化的不同电位依赖性以及对外部四乙铵和4-氨基吡啶的敏感性进行了分离。通过Hodgkin-Huxley方程描述了快速失活的钾电流,慢速失活的钾电流和非失活的延迟整流器电流的动力学和稳态特性的电位依赖性。瞬态快速失活钾电流在最负的膜电位处被激活,并且在外部溶液中存在10 mM四乙铵时不会降低。 4-氨基吡啶(2 mM)对该电流产生80%的抑制作用。快速失活钾电流的激活通过将单个指数提高到四次幂来适当描述。在-30至+40 mV的电压范围内,激活的时间常数从4毫秒变为1毫秒。在相同的电位范围内,灭活的时间常数从35毫秒降低到15毫秒。用于将Boltzmann方程拟合为稳态激活平均值的参数为V1 / 2 = -20mV,k = 11.8mV,而对于稳态失活V1 / 2 = -85mV,k = -9.8mV。瞬时缓慢失活钾电流的激活阈值为-40至-30 mV。在2 mM 4-氨基吡啶处,慢钾电流的降低为55%。在细胞外施用10 mM四乙铵的效果较差,并且减少了40%。缓慢失活钾电流的激活也通过提高到四次幂的单个指数函数来描述。激活的时间常数从膜电位为-10 mV的12 ms降至电位为60 mV的4 ms。缓慢失活钾电流的失活由两个指数描述。快速指数的时间常数范围从-20 mV时的300 ms到+60 mV时的160 ms。较慢的指数也与电势有关,在相同电势下,其时间常数范围约为2600至1600 ms。用于稳态值的Boltzmann方程拟合的参数分别为稳态激活和灭活的V1 / 2 = -12.8 mV,k = 13.4 mV和V1 / 2 = -54.6 mV,k = -12 mV。非灭活的延迟整流器钾电流在最正的膜电位下被激活。在4-氨基吡啶存在下,这种非灭活电流没有改变。细胞外四乙铵(10 mM)导致该电流降低70%。非灭活钾电流的激活通过一个指数升至四次幂来描述。激活的时间常数从-5 mV的85 ms到45 mV的30 ms不等。在10到+60 mV的电压范围内的15s测试电位期间,未观察到时间依赖性灭活。活化行为的特征在于V1 / 2 = 15.3mV,k = 12.5mV。研究了三组动物的这些钾电流的密度:出生后1、5至6天和14-15天。在每个年龄组中检查了五十个细胞。在每个研究的神经元中都发现了所有三种钾电流。在个体发育过程中,缓慢和快速失活钾电流的平均密度增加。非灭活的延迟整流钾电流的密度在个体发育的第一周下降,此后没有变化。

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