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[二价阳离子诱导甲状旁腺细胞膜电位中的协同现象]

[Cooperative phenomena in the membrane potential of parathyroid cells induced by divalent cations].

作者信息

Hirose T

出版信息

Nihon Seirigaku Zasshi. 1985;47(10):673-87.

PMID:4093891
Abstract

Membrane potentials of mouse parathyroid cells were measured by means of the intracellular microelectrode method. The membrane potential in external Krebs solution containing 2.5 mM of Ca++ was -23.6 +/- 0.4 mV (mean +/- standard error of mean). The low concentration of Ca++ (1.0 mM) caused hyperpolarization of the membrane potential to -61.7 +/- 0.8 mV. The membrane potential was proportional to the logarithm of the concentration of K ion in the solution of low Ca ion. The concentration of external Na+, C1- and HPO4-- had no effect on the membrane potential. The sigmoidal transition of membrane potentials was induced by the change of Ca ion concentration in the range from 2.5 to 1.0 mM. The change of the membrane potentials in low Ca ion is originated from increase in potassium permeability of the cell membrane. The similar sigmoidal changes of the membrane potentials were observed in the solution containing 4 to 3 mM of Sr ion. The Mg and Ba ion showed smaller effect on the membrane potential. The Goldman equation was extended to divalent ions. Appling the extended membrane potential equation, ratios of the permeability coefficients were obtained as follows: PK/PCa = 0.067 for 2.5 mM Ca++, 0.33 for 1.0 mM Ca++; PK/PSr = 0.08 for 4 mM Sr++ and 0.4 for 3 mM Sr++; PK/PMg = 0.5; PK/PBa = 0.67 for all range of concentration. The Hill constants of Sr ion and Ca ion were 20; the relationship between Sr ion and Ca ion was competitive. The Hill constants of Mg and Ba ion were 1 each. The Hill constant of Ca ion was depend of the temperature; nmax = 20 at 36 degrees C, n = 9 at 27 degrees C, n = 2 at 22 degrees C. The enthalpy of Ca-binding reaction was obtained from the Van't Hoff plot as 0.58 kcal. The activation energies of the K+ permeability increase were obtained from the Arrhenius plots as 3.3 kcal and 4 kcal. The difference, 0.7 kcal, corresponds to the enthalpy change of this reaction, of which value is close to that of the Ca-binding reaction.

摘要

采用细胞内微电极法测量了小鼠甲状旁腺细胞的膜电位。在含有2.5 mM钙离子的外部 Krebs 溶液中,膜电位为-23.6±0.4 mV(平均值±平均标准误差)。低浓度的钙离子(1.0 mM)导致膜电位超极化至-61.7±0.8 mV。在低钙离子溶液中,膜电位与钾离子浓度的对数成正比。外部钠离子、氯离子和磷酸氢根离子的浓度对膜电位没有影响。钙离子浓度在2.5至1.0 mM范围内的变化诱导了膜电位的S形转变。低钙离子条件下膜电位的变化源于细胞膜钾离子通透性的增加。在含有4至3 mM锶离子的溶液中也观察到了类似的膜电位S形变化。镁离子和钡离子对膜电位的影响较小。将戈德曼方程扩展到二价离子。应用扩展的膜电位方程,得到的通透性系数比值如下:对于2.5 mM钙离子,PK/PCa = 0.067;对于1.0 mM钙离子,PK/PCa = 0.33;对于4 mM锶离子,PK/PSr = 0.08;对于3 mM锶离子,PK/PSr = 0.4;PK/PMg = 0.5;对于所有浓度范围,PK/PBa = 0.67。锶离子和钙离子的希尔常数均为20;锶离子和钙离子之间的关系是竞争性的。镁离子和钡离子的希尔常数均为1。钙离子的希尔常数取决于温度;在36℃时,nmax = 20;在27℃时,n = 9;在22℃时,n = 2。从范特霍夫图得到钙结合反应的焓为0.58千卡。从阿累尼乌斯图得到钾离子通透性增加的活化能为3.3千卡和4千卡。差值0.7千卡对应于该反应的焓变,其值与钙结合反应的值接近。

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