| Electrochemical Properties of Hydrated Cation-Selective Glass Membrane Biophysical Journal, Volume 14, Issue 1, 1 January 1974, Pages 46-68 Chin Ok Lee and Harry A. Fozzard Abstract Electrochemical properties of cation-selective glass microelectrodes made from NAS were studied. There was a marked fall in electrical resistance of the microelectrodes stored in 3 M KCl solution (aging). The resistance was in the range of 2×10 to 10 Ω, which were much lower than those estimated from the electrical resistivity of dry glass for the equivalent dimensions of microelectrode working tips. This fall in resistance was accompanied by an increase in microelectrode selectivity for K. The low resistance and increased K selectivity are desirable features that make the microelectrode more suitable for application to biologic studies. The changes in microelectrode resistance and selectivity were interpreted to be due to hydration of the entire thickness of the glass membrane, resulting in a change in the field strength of anionic sites and formation of ionic channels in the glass membrane. Thus, the fall in resistance is explained by decrease in energy barrier, which is equivalent to the activation energy of interaction between the cations and anionic sites in the glass membrane. Some of the microelectrodes showed a transient depolarization that resembled the action potential of a biological membrane. This transient depolarization was associated with the changes in microelectrode resistance and selectivity. The transient depolarizations suggest the temporary development of wide channels in the membrane permitting free movement of hydrated cations according to the bulk electrochemical gradient. Abstract | PDF (1668 kb) |
| Intracellular microelectrode measurements in small cells evaluated with the patch clamp technique Biophysical Journal, Volume 50, Issue 6, 1 December 1986, Pages 1203-1209 C. Ince, E. van Bavel, B. van Duijn, K. Donkersloot, A. Coremans, D.L. Ypey and A.A. Verveen Abstract Microelectrode penetration of small cells leads to a sustained depolarization of the resting membrane potential due to a transmembrane shunt resistance (Rs) introduced by the microelectrode. This has led to underestimation of the resting membrane potential of various cell types. However, measurement of the fast potential transient occurring within the first few milliseconds after microelectrode penetration can provide information about pre-impalement membrane electrophysiological properties. We have analyzed an equivalent circuit of a microelectrode measurement to establish the conditions under which the peak of the impalement transients (Ep) approaches the pre-impalement resting membrane potential (Em) of small cells most closely. The simulation studies showed that this is the case when the capacitance of the microelectrode is low and the membrane capacitance of the cell high. In experiments performed to assess the reliability of Ep as a measure of Em, whole-cell patch clamp measurements were performed in the current clamp mode to monitor, free from the effects of Rs, Em in cultured human monocytes. Microelectrode impalement of such patch clamped cells and measurement of Ep made it possible to detect correlation between Ep and Em and showed that for small cells such as human monocytes Ep is on average 6 mV less negative than the resting membrane potential. Abstract | PDF (876 kb) |
| Resistive artifacts in liquid-ion exchanger microelectrode estimates of Na+ activity in epithelial cells Biophysical Journal, Volume 31, Issue 1, 1 July 1980, Pages 127-138 S.A. Lewis and N.K. Wills Abstract In experiments on the rabbit urinary bladder epithelium we have identified an electrical artifact in certain liquid ion-sensitive microelectrodes. This artifact arises from the high electrical resistance of the ion-sensitive resins which in some cases are comparable to the resistance of the microelectrode glass wall. For Na+-sensitive microelectrodes this situation led to shunting of the exchanger potential and consequently artifactually high calculations of intracellular Na+ in the rabbit urinary bladder epithelium. A method for minimizing this shunting effect is described. After reduction of the shunt the frequency response of the Na+-sensitive microelectrode was increased and the estimated ai Na+ was decreased to 7 mM. Abstract | PDF (672 kb) |
Copyright © 1985 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 48, Issue 6, 983-995, 1 December 1985
doi:10.1016/S0006-3495(85)83861-3
Research Article
D.L. Alkon and M. Sakakibara
Light-induced currents were measured with a two-microelectrode voltage clamp of type B photoreceptor somata, which had been isolated by axotomy from all synaptic interactions as well as from all membranes capable of generating impulse activity. In artificial seawater (ASW), light elicited a transient early inward current, INa+, which depended on Na+o and had a linear current-voltage relation and an extrapolated reversal potential of 30–40 mV (absolute). In 0-Na+ ASW, light elicited a transient short-latency outward current that dependent on K+o, increased exponentially with more positive voltages (greater than or equal to -40 mV), and reversed at -70 to -75 mV. This outward current was not blocked by Ca++ channel blockers (e.g., Cd++, Co++) or substitution of Ba++o, for Ca++o, but was reduced by iontophoretic injection of EGTA. In both ASW and 0-Na+ ASW, light also elicited a delayed, apparently inward current, which was associated with a decreased conductance, depended on K+o, increased exponentially with more positive voltages (greater than or equal to -40 mV), reversed at the equilibrium potential for K+ flux in elevated K+o was eliminated by substitution of Ba++o for Ca++o, and was greatly reduced by Cd++o or Co++o. Thus, light elicited an early Ca++-dependent K+ current, IC, and a prolonged decrease of IC. Iontophoretic injection of Ca++ through a third microelectrode caused prolonged reduction of both IC and the light-induced decrease of IC, but did not alter ICa++ or the current-voltage relation of IC. Ruthenium red (1 microM) in the external medium caused a prolongation of the light-induced decrease of IC. Iontophoretic injection of EGTA often eliminated the light-induced IC decrease while decreasing peak IC (during depolarizing steps to -5 or 0 mV) by less than one-half. EGTA injection, on the average, did not affect steady state IC but reduced the light-induced decrease of steady state IC to approximately one-third of its original magnitude. The prolonged IC decrease, elicited by dim light in the absence of light-induced IC or INa+, was more completely eliminated by EGTA injection. It was concluded that light, in addition to inducing a transient inward Na+ current, causes both a transient increase and a prolonged decrease of IC via elevation of Ca++i.