ArticleThe Journal of membrane biology1988
Voltage- and time dependence of apical membrane conductance during current clamp in Necturus gallbladder epithelium.
Article in The Journal of membrane biology, 1988. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Cell swelling activates the K+ conductance and inhibits the Cl- conductance of the basolateral membrane of cells from a leaky epithelium.The Journal of general physiology · 1997Article
- Pseudo-streaming potentials in Necturus gallbladder epithelium. I. Paracellular origin of the transepithelial voltage changes.The Journal of general physiology · 1992Article
- Electrophysiological effects of basolateral [Na+] in Necturus gallbladder epithelium.The Journal of general physiology · 1992Article
- Electrophysiological effects of extracellular ATP on Necturus gallbladder epithelium.The Journal of general physiology · 1991Article
- Effects of changes in mucosal solution Cl- or K+ concentration on cell water volume of Necturus gallbladder epithelium.The Journal of general physiology · 1991Article
- Cytosolic pH regulates maxi K+ channels in Necturus gall-bladder epithelial cells.The Journal of physiology · 1991Article
- Voltage-dependent currents in isolated cells of the frog retinal pigment epithelium.The Journal of physiology · 1990Article
- Maxi K+ channels and their relationship to the apical membrane conductance in Necturus gallbladder epithelium.The Journal of general physiology · 1990Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
The effects of short (1 sec) and long (1 min) transepithelial current clamps on membrane voltages and resistances of Necturus gallbladder were investigated. Transepithelial and cell membrane current-voltage relationships determined from 1-sec clamps revealed that: a) depolarization of the apical membrane voltage (Vmc) results in a marked decrease in apical membrane fractional resistance (fRa), whereas hyperpolarization of Vmc results in either no change in fRa or a small increase, and b) the voltage-dependent changes in fRa are essentially complete within 500 msec. Exposure of the tissue to 5 mM TEA+ on the mucosal side caused no significant change in baseline Vmc (-69 +/- 2 mV) and yet virtually abolished the voltage dependence of fRa. A possible interpretation of these results is that two types of K+ channels exist in the apical membrane, with different voltage dependencies and TEA+ sensitivities. Acidification or Ba2+ addition to the mucosal solution also reduced the voltage-dependent changes in fRa. The time courses of the changes in fRa and in the cable properties of the epithelium were assessed during 1-min transepithelial current clamps (+/- 200 microA/cm2). No secondary change in fRa was observed with mucosa-to-serosa currents, but a slow TEA+-sensitive decrease in fRa (half-time of seconds) was evident with serosa-to-mucosa currents. Cable analysis experiments demonstrated that the initial (less than 500 msec) voltage-dependent decrease in fRa is due to a fall in apical membrane resistance. The later decrease in fRa is due to changes in both cell membrane resistances attributable to the increase in transcellular current flow resulting from a fall in paracellular conductance. The voltage dependence of the apical membrane conductance is a more significant problem in estimating fRa than the current-induced effects on the lateral intercellular spaces. In principle, TEA+ can be used to prevent the nonlinear behavior of Ra during measurements of the voltage divider or membrane resistance ratio.
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