Baud C, Barish M E
Dev Biol. 1984 Oct;105(2):423-34. doi: 10.1016/0012-1606(84)90299-9.
A voltage-gated hydrogen ion-selective conductance has been previously described in the immature oocyte of the urodele amphibian Ambystoma. The present study was prompted by reports that changes in membrane voltage and internal pH, as well as in internal sodium ion concentration, occur during the hormone-induced maturation of oocytes from other amphibians. As activation of membrane currents might mediate changes in internal ion concentrations in addition to altering the membrane voltage, microelectrode recording techniques have been employed to examine changes in membrane conductances which occur during maturation of Ambystoma oocytes. It was observed that during the first 5 hr of maturation the magnitude of the hydrogen ion conductance gradually decreased, and that subsequently there was an increase in the amplitude of a voltage-dependent noninactivating sodium conductance. After 6 to 7 hr, after the loss of the hydrogen conductance and at about the time of germinal vesicle breakdown, the resting potential of the oocyte spontaneously shifted from approximately -10 mV to approximately +30 mV, where it remained until at least 24 hr after the initiation of maturation. This voltage transition was due to the appearance of mechanisms generating inward current in the oocyte membrane; part of this inward current was due to the tonic activation of the sodium conductance. Changes in internal pH and internal sodium ion concentration occurred during maturation, as judged from shifts in the reversal potentials of both hydrogen and sodium currents. A gradual decrease in internal hydrogen ion concentration was observed up until the time of disappearance of the hydrogen conductance (change in internal pH from about 7.15 in immature oocytes to about 7.40 by 3 hr after application of progesterone). This was followed, as sodium conductance increased, by an apparent rise in the internal sodium ion concentration (from about 6 mM to about 17 mM by 10 hr postprogesterone).
先前已在有尾两栖动物美西螈未成熟的卵母细胞中描述过电压门控氢离子选择性电导。本研究是由一些报道引发的,这些报道称在其他两栖动物卵母细胞的激素诱导成熟过程中,膜电压、内部pH值以及内部钠离子浓度会发生变化。由于膜电流的激活除了改变膜电压外,还可能介导内部离子浓度的变化,因此已采用微电极记录技术来检测美西螈卵母细胞成熟过程中发生的膜电导变化。观察到在成熟的最初5小时内,氢离子电导的幅度逐渐降低,随后电压依赖性非失活钠电导的幅度增加。在6至7小时后,氢离子电导消失且大约在生发泡破裂时,卵母细胞的静息电位自发地从约-10 mV转变为约+30 mV,并一直保持到成熟开始后至少24小时。这种电压转变是由于卵母细胞膜中产生内向电流的机制出现;部分这种内向电流是由于钠电导的持续性激活。根据氢离子和钠电流反转电位的变化判断,成熟过程中内部pH值和内部钠离子浓度发生了变化。在氢离子电导消失之前,观察到内部氢离子浓度逐渐降低(内部pH值从未成熟卵母细胞中的约7.15在应用孕酮后3小时变为约7.40)。随着钠电导增加,随后内部钠离子浓度明显升高(在应用孕酮后10小时从约6 mM升至约17 mM)。