A Fundamental Question About Electrical Potential Profile in Interfacial Region of Biological Membrane Systems

Author(s):  
V. S. Vaidhyanathan
1975 ◽  
Vol 24 (1) ◽  
pp. 341-363 ◽  
Author(s):  
C. H. van Os ◽  
J. F. G. Slegers

1989 ◽  
Vol 257 (4) ◽  
pp. C722-C726 ◽  
Author(s):  
M. M. Reddy ◽  
P. M. Quinton

The electrophysiological properties of reabsorptive sweat duct (RSD) cells from normal and cystic fibrosis (CF) subjects were studied using intracellular microelectrodes. The apical membrane potential (Va) of CF duct cells was reversed in "polarity" (+28.0 +/- 2.4 mV, n = 46) compared with normal duct cells (-24.9 +/- 0.4 mV, n = 145), and the basolateral membrane potential (Vb) of CF cells was hyperpolarized significantly (-50.1 +/- 1.2 mV, n = 46) in comparison to normal cells (-34.6 +/- 0.4 mV, n = 145). The substitution of the impermeant anion gluconate for Cl- in the lumen of the normal duct depolarized Va from -24.9 +/- 1.1 to 8.9 +/- 3.1 mV (n = 18) and hyperpolarized Vb from -34.3 +/- 1.1 to -55.6 +/- 3.7 mV (n = 18), which mimicked the cell electrical potential profile of CF ducts even in the presence of Cl-. Cl- substitution in the bath depolarized Vb of normal ducts by 22.5 +/- 2.6 mV (n = 24), while hyperpolarizing Va by -3.4 +/- 1.6 mV (n = 24). The response of the electrical profiles of CF cells to Cl- substitution in either the lumen or the bath was significantly reduced compared with normal cells. The effect of the Na+ conductance blocker amiloride (10(-4) M) on Vb was not significantly different in CF (delta Vb = -26.4 +/- 3.8 mV, n = 9) vs. normal (delta Vb = -27.6 +/- 2.5 mV, n = 30) cells.(ABSTRACT TRUNCATED AT 250 WORDS)


2020 ◽  
Author(s):  
Suhariningsih ◽  
Retno Nurlilawati Aisyah ◽  
Nurul Fitriyah ◽  
Suryani Dyah Astuti ◽  
Tri Anggono Prijo ◽  
...  

F1000Research ◽  
2020 ◽  
Vol 9 ◽  
pp. 676
Author(s):  
Marco Arieli Herrera-Valdez

Biological membranes mediate different physiological processes necessary for life, many of which depend on ion movement. In turn, the difference between the electrical potentials around a biological membrane, called transmembrane potential, or membrane potential for short, is one of the key biophysical variables affecting ion movement. Most of the existing equations that describe the change in membrane potential are based on analogies with resistive-capacitive electrical circuits. These equivalent circuit models assume resistance and capacitance as measures of the permeable and the impermeable properties of the membrane, respectively. These models have increased our understanding of bioelectricity, and were particularly useful at times when the basic structure, biochemistry, and biophysics of biological membrane systems were not well known. However, the parts in the ohmic circuits from which equations are derived, are not quite like the biological elements present in the spaces around and within biological membranes. Using current, basic knowledge about the structure, biophysics, and biochemical properties of biological membrane systems, it is shown here that it is possible to derive a simple equation for the transmembrane potential. Of note, the resulting equation is not based on electrical circuit analogies. Nevertheless, the classical model for the membrane potential based on an equivalent RC-circuit is recovered as a particular case, thus providing a mathematical justification for the classical models. Examples are presented showing the effects of the voltage dependence of charge aggregation around the membrane, on the timing and shape of neuronal action potentials.


1964 ◽  
Vol 47 (4) ◽  
pp. 795-808 ◽  
Author(s):  
Guillermo Whittembury

The electrical potential profile of the isolated toad skin was recorded, in vitro, by impalement with micropipette-electrodes, when both sides of the skin were bathed with sulfate-Ringer. The outer side of the skin was some 110 mv negative with respect to the inner side. Upon impalement from the outer side, two main positive steps of 40 to 70 mv each were found to form the skin potential. The site of measurement of each potential difference was permanently marked in the tissue during recording, by deposition of carmine from the micropipette tip using iontophoresis. Serial histological sections of the skin were prepared and search was then made of the carmine deposits 2 to 6 µ in size, under phase contrast microscopy. By this method the main steps were located at the outer and the inner sides of the stratum germinativum cells. The DC resistances between the micropipette tip and the bathing solutions were measured during the recording of each potential difference. The resistance at the outer side of the stratum germinativum cells, of 1.09 kilohm. cm2, was larger than that at their inner side, of 0.30 kilohm. cm2. The stratum germinativum cells maintained a potential difference of -34 mv during short-circuiting of the skin.


2020 ◽  
Author(s):  
Joanna Dziadkowiec ◽  
Hsiu-Wei Cheng ◽  
Anja Røyne ◽  
Markus Valtiner

<p>When two mineral surfaces are in close contact, nanometers to microns apart, the proximity of another surface can significantly influence the pathways of chemical reactions happening in the interfacial region. Apart from affecting the kinetics of dissolution and nucleation reactions in spatial confinement, the proximity of charged surfaces can lead to electrochemically induced recrystallization processes. The latter may happen in an asymmetric system, in which two surfaces have a dissimilar surface charge. The charge and mass transferred during electrochemical reactions can induce dissolution or growth of solids and can significantly affect the local topography of surfaces, causing them to smooth out or to roughen. In this work, we present the experimental study of reactive mineral interfaces, immersed in geologically relevant electrolyte solutions, obtained with the electrochemical surface forces apparatus (EC-SFA). EC-SFA setup consists of one mineral surface and one gold surface (working electrode), the surface charge of which is controlled by applying an electrical potential. EC-SFA can, therefore, monitor electrochemically induced surface recrystallization processes. As the SFA technique is based on white light interferometry measurements, the changes in mineral thickness during recrystallization can be determined with an accuracy better than a nanometer over micrometer-large contact regions. Moreover, SFA allows in situ measurement of surface forces acting between mineral surfaces, which can provide additional information about how the surface reactivity influences the cohesion between mineral surfaces by modifying adhesive and repulsive forces acting between them at small separations.</p>


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