Wind B E, Walsh S, Patterson J W
Department of Physiology, University of Connecticut Health Center, Farmington 06032.
Exp Eye Res. 1988 Feb;46(2):117-30. doi: 10.1016/s0014-4835(88)80070-8.
Earlier work with the vibrating probe demonstrated the existence of outward potassium currents at the equator and inward sodium currents at the optical poles of the lens. By adding microelectrodes to the system, it is possible to relate steady currents (J) to the potential difference (PD) measured with a microelectrode. By injecting an outward current (I), it is possible to determine resistances and also the PD at which the steady outward potassium current becomes zero (PDJ = 0). At this PD the concentration gradient for potassium efflux and the electrical gradient for potassium influx are balanced so that there is no net flow of potassium across the membranes associated with the production of J. The PDJ = 0 for 18 rat lenses was 86 mV and that for 12 frogs lenses was -95 mV. This agrees with the potassium equilibrium potential and provides strong evidence to support the view that the outward equatorial current, J, is a potassium current. With the injection of outward current, I, the PD becomes more negative, the outward equatorial current, J, decreases, and the inward current at the optical poles increases. This suggests that there are separate electrical loops for K+ and Na+ that are partially linked by the Na, K-pump. Using Ohm's law, it is possible to calculate the input resistance (R = delta PD/I), the resistance related to the production of J (RJ = delta PD/delta J), and the effect of the combined resistances (delta J/I). The driving force for J can be estimated (PDJ = 0-PD). The relationships among currents, voltages and resistance can be used to determine the characteristics of the membranes that are associated with the outward potassium current observed at the equator. The effects of graded deformation of the lens were determined. The effects were reversible. The sites of inward and outward currents were not altered. Following deformation, the equatorial current, J, increased, and the PD became less negative. The PDJ = 0 remains the same so the ratio of K+ concentrations across the membrane responsible for J is unchanged. Therefore, the decrease in PD is ascribed to an increase in Na+ permeance with a resultant increase in driving force accounting for the increase in J.
早期使用振动探针的研究表明,在晶状体赤道处存在外向钾电流,在晶状体光极处存在内向钠电流。通过在该系统中添加微电极,就能够将稳定电流(J)与用微电极测量的电位差(PD)联系起来。通过注入外向电流(I),可以确定电阻以及稳定外向钾电流变为零(PDJ = 0)时的电位差。在这个电位差下,钾外流的浓度梯度和钾内流的电梯度达到平衡,因此没有与J产生相关的钾跨膜净流动。18个大鼠晶状体的PDJ = 0为86 mV,12个青蛙晶状体的PDJ = 0为 -95 mV。这与钾平衡电位相符,并为支持赤道外向电流J是钾电流这一观点提供了有力证据。随着外向电流I的注入,PD变得更负,赤道外向电流J减小,光极处的内向电流增加。这表明存在K +和Na +的独立电回路,它们通过钠钾泵部分相连。使用欧姆定律,可以计算输入电阻(R = ΔPD / I)、与J产生相关的电阻(RJ = ΔPD / ΔJ)以及组合电阻的影响(ΔJ / I)。J的驱动力可以估算(PDJ = 0 - PD)。电流、电压和电阻之间的关系可用于确定与在赤道处观察到的外向钾电流相关的膜特性。确定了晶状体分级变形的影响。这些影响是可逆的。内向和外向电流的位置没有改变。变形后,赤道电流J增加,PD变得不那么负。PDJ = 0保持不变,因此负责J的跨膜K +浓度比不变。因此,PD的降低归因于Na +通透性的增加,导致驱动力增加,这解释了J的增加。