The effect of amiloride on the transepithelial potential difference of the distal tubule of the rat kidney

1976 ◽  
Vol 361 (3) ◽  
pp. 251-254 ◽  
Author(s):  
Lindsay J. Barratt
Keyword(s):  
Rat Kidney ◽  
Distal Tubule ◽  
Potential Difference ◽  
Transepithelial Potential ◽  
Transepithelial Potential Difference

scholarly journals Transepithelial potential difference profile of the distal tubule of the rat kidney

1975 ◽  
Vol 8 (6) ◽  
pp. 368-375 ◽  
Author(s):  
Lindsay J. Barratt ◽  
Floyd C. Rector ◽  
Juha P. Kokko ◽  
C. Craig Tisher ◽  
Donald W. Seldin
Keyword(s):  
Rat Kidney ◽  
Distal Tubule ◽  
Potential Difference ◽  
Transepithelial Potential ◽  
Transepithelial Potential Difference

Factors influencing transepithelial potential difference in mammalian distal tubule

1978 ◽  
Vol 234 (3) ◽  
pp. F182-F191 ◽  
Author(s):  
J. P. Hayslett ◽  
E. L. Boulpaep ◽  
G. H. Giebisch
Keyword(s):  
Electrical Properties ◽  
Cell Membrane ◽  
Distal Tubule ◽  
Potential Difference ◽  
Ion Concentration ◽  
Luminal Cell ◽  
Transepithelial Potential ◽  
Transepithelial Potential Difference ◽  
Factors Influencing ◽  
Average Slope

Studies were performed to examine some electrical properties of the mammalian distal tubule. Experiments were performed to evaluate the influence of changes in ion concentration in luminal fluid on transepithelial potential difference. Variations in the concentration of Na+ and K+, near the physiologic range, resulted in only modest changes in potential difference. During changes in Na+ the average slope, deltaV/ln C2/C1, was -1.52 +/- 0.39 mV and during variations in K+ the slope was -5.60 +/- 0.95 mV. Changes in Cl- concentration had no effect on transepithelial potential difference. Since the sum of transferase numbers did not equal 1, it seems likely that potential difference is influenced by a shunt current due to cellular rheogenic pumps. These data, therefore, indicate that variations in ion concentration in tubular fluid of the mammalian distal tubule do not significantly influence the resting transepithelial potential difference, and they suggest that analysis of permselective properties of the luminal cell membrane by transepithelial electrophysiologic approaches is probably invalid.

Electrochemical profile of K+ and Na+ in the amphibian early distal tubule

1985 ◽  
Vol 248 (2) ◽  
pp. F266-F271
Author(s):  
J. Teulon ◽  
P. Froissart ◽  
T. Anagnostopoulos
Keyword(s):  
Distal Tubule ◽  
Electrochemical Potential ◽  
Potential Difference ◽  
Raw Data ◽  
Transepithelial Potential ◽  
Transepithelial Potential Difference ◽  
Ion Activities

Double-barreled microelectrodes selective to either potassium or sodium were used to determine the transepithelial potential difference (VTE) and the intraluminal activity of potassium (alpha LuK) or sodium (alpha LuNa) in the early distal tubule (EDT) of Triturus waltlii in vivo; luminal activities were compared with the corresponding plasma ion activities, alpha PtK and alpha PtNa. The transepithelial equilibrium potentials for potassium (EK(TE] and sodium (ENa(TE] were computed from the respective transmural chemical distributions: they were used to assess the transepithelial electrochemical potential differences [(V-EK)TE and (V-ENa)TE]. By dividing the raw data into three groups of 30% total tubular length (0-30, 31-60, 61-90%), the following results were obtained. 1) VTE increases from +15 to +20 mV (lumen positive) between the first and second portion of the EDT but remains constant thereafter. 2) The alpha LuK/alpha PtK ratio decreases steadily along the EDT from 1.92 to 1.66 and then to 1.32. 3) The values of alpha LuNa/alpha PtNa in the same three subdivisions are 0.79, 0.44, and 0.45. 4) The (V-EK)TE difference is largely positive along the whole EDT: +32, +33, and +27 mV. 5) The (V-ENa)TE difference declines from +9 mV (first portion) to values statistically not different from zero in the last two thirds of the EDT.(ABSTRACT TRUNCATED AT 250 WORDS)

Nitric oxide-mediated regulation of transepithelial sodium and chloride transport in murine nasal epithelium

1999 ◽  
Vol 276 (3) ◽  
pp. L466-L473 ◽  
Author(s):  
Heather L. Elmer ◽  
Kristine G. Brady ◽  
Mitchell L. Drumm ◽  
Thomas J. Kelley
Keyword(s):  
Nitric Oxide ◽  
Chloride Transport ◽  
Chloride Secretion ◽  
Inos Expression ◽  
Potential Difference ◽  
Nasal Epithelium ◽  
Sodium Absorption ◽  
No Production ◽  
Transepithelial Potential ◽  
Transepithelial Potential Difference

Transepithelial ion transport is regulated by a variety of cellular factors. In light of recent evidence that nitric oxide (NO) production is decreased in cystic fibrosis airways, we examined the role of NO in regulating sodium and chloride transport in murine nasal epithelium. Acute intervention with the inducible NO synthase (iNOS)-selective inhibitor S-methylisothiourea resulted in an increase of amiloride-sensitive sodium absorption observed as a hyperpolarization of nasal transepithelial potential difference. Inhibition of iNOS expression with dexamethasone also hyperpolarized transepithelial potential difference, but only a portion of this increase proved to be amiloride sensitive. Chloride secretion was significantly inhibited in C57BL/6J mice by the addition of both S-methylisothiourea and dexamethasone. Mice lacking iNOS expression [NOS2(−/−)] also had a decreased chloride-secretory response compared with control mice. These data suggest that constitutive NO production likely plays some role in the downregulation of sodium absorption and leads to an increase in transepithelial chloride secretion.

Calcium secretion in canine tracheal mucosa

1985 ◽  
Vol 59 (4) ◽  
pp. 1191-1195 ◽  
Author(s):  
F. J. Al-Bazzaz ◽  
T. Jayaram
Keyword(s):  
Short Circuit ◽  
Short Circuit Current ◽  
Open Circuit ◽  
Potential Difference ◽  
Secretory Process ◽  
Metabolic Inhibitor ◽  
Tracheal Mucosa ◽  
Transepithelial Potential ◽  
Transepithelial Potential Difference

Calcium (Ca) affects many cellular functions of the respiratory tract mucosa and might alter the viscoelastic properties of mucus. To evaluate Ca homeostasis in a respiratory epithelium we investigated transport of Ca by the canine tracheal mucosa. Mucosal tissues were mounted in Ussing-type chambers and bathed with Krebs-Henseleit solution at 37 degrees C. Unidirectional fluxes of 45Ca were determined in tissues that were matched by conductance and short-circuit current (SCC). Under short-circuit conditions there was a significant net Ca secretion of 1.82 +/- 0.36 neq . cm-2 . h-1 (mean +/- SE). Under open-circuit conditions, where the spontaneous transepithelial potential difference could attract Ca toward the lumen, net Ca secretion increased significantly to 4.40 +/- 1.14 compared with 1.54 +/- 1.17 neq . cm-2 . h-1 when the preparation was short-circuited. Addition of a metabolic inhibitor, 2,4-dinitrophenol (2 mM in the mucosal bath), decreased tissue conductance and SCC and slightly decreased the unidirectional movement of Ca from submucosa to lumen. Submucosal epinephrine (10 microM) significantly enhanced Ca secretion by 2.0 +/- 0.63 neq . cm-2 . h-1. Submucosal ouabain (0.1 mM) failed to inhibit Ca secretion. The data suggest that canine tracheal mucosa secretes Ca; this secretory process is augmented by epinephrine or by the presence of a transepithelial potential difference as found under in vivo conditions.

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