scholarly journals Active Transport of Sodium by the Isolated Midgut of Hyalophora Cecropia

1971 ◽  
Vol 54 (1) ◽  
pp. 269-274
Author(s):  
W. R. HARVEY ◽  
K. ZERAHN
Keyword(s):  
Active Transport ◽  
Sodium Transport ◽  
Transport Mechanism ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Large Current ◽  
Sodium Flux ◽  
Hyalophora Cecropia ◽  
Sodium Solution

1. Sodium and lithium are actively transported by the isolated midgut of Hyalophora cecropia. 2. The short-circuit current in 32 mM sodium solution is about half of that in 32 mM potassium solution. 3. The sodium flux measured with 22Na from blood-side to lumen accounts for all of the short-circuit current and is 19 times the flux from lumen to blood-side. 4. In a solution containing 16 mM potassium and 16 mM sodium there is no transport of sodium, although a large current remains. 5. The sodium transport mechanism is not sensitive to ouabain.

Ion transport across rumen and omasum epithelium

1971 ◽  
Vol 262 (842) ◽  
pp. 301-305 ◽  
Keyword(s):  
Active Transport ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Chloride Ions ◽  
Rumen Epithelium ◽  
Sodium Flux ◽  
Sodium System ◽  
Chloride Pump ◽  
Net Flux ◽  
Cattle And Sheep

The interior of the rumen in cattle and sheep is normally maintained at a potential of about — 40 mV relative to the blood. This potential depends primarily on the occurrence of an active transport of sodium from rumen to blood, since the potential, short-circuit current and the net sodium flux are simultaneously abolished by anoxia, ouabain and removal of sodium from the bathing solutions. There is an appreciable net flux of potassium from blood to rumen. There is also a substantial active transport of chloride in the same direction as sodium and it can be reduced by treatment with acetazolamide without affecting the potential or the sodium system. Nevertheless, sodium transport is reduced by the removal of chloride ions. Omasum epithelium is similar to rumen epithelium. However, the chloride pump appears to work in both directions in this tissue. Short-circuited omasum epithelium can also transport magnesium from omasum to blood.

Stimulation of sodium transport in toad bladder by acidification of mucosal medium

1964 ◽  
Vol 207 (3) ◽  
pp. 547-552 ◽  
Author(s):  
Alexander Leaf ◽  
Albert Keller ◽  
Eleanor F. Dempsey
Keyword(s):  
Urinary Bladder ◽  
Sodium Transport ◽  
Short Circuit ◽  
Electrical Potential ◽  
Short Circuit Current ◽  
Ph Optimum ◽  
Tissue Ph ◽  
Mucosal Acidification ◽  
Sodium Flux ◽  
Stimulation Of

The short-circuit current, sodium flux, and electrical potential across the isolated urinary bladder of the toad were stimulated by acidification of the medium bathing the mucosal or urinary surface of the bladder. By contrast the transport of chloride, potassium, urea, and water across the bladder was unaffected by similar acidification. The pH optimum for this action was approximately 5.5. The tissue pH, as determined by the distribution of DMO-C14, was not detectably affected by mucosal acidification.

Active Transport of Potassium and Oxygen Consumption in the Isolated Midgut of Hyalophora Cecropia

1967 ◽  
Vol 46 (2) ◽  
pp. 235-248
Author(s):  
W. R. HARVEY ◽  
J. A. HASKELL ◽  
K. ZERAHN
Keyword(s):  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Active Transport ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Na Transport ◽  
Maximum Value ◽  
Flux Measurements ◽  
Hyalophora Cecropia ◽  
K Transport

1. Flux measurements with 42K reveal that in the isolated midgut of Hyalophora cecropia 90 to 100 % of the short-circuit current is carried by the active transport of potassium from the blood-side to the lumen. 2. When K-transport is strongly depressed, either by withholding potassium from the blood side or by imposing a large positive potential on the lumen, the oxygen uptake of the isolated gut remains virtually unchanged. If the K-transport were to be energized by the negligible increase in oxygen uptake about 40 µ-equiv. of potassium would have to be transported for every µ-equiv. of extra oxygen taken up. This ratio of K-transport to oxygen uptake is thermodynamically impossible. 3. The ratio of potassium transported to total oxygen consumed when the midgut is bathed with 32 mM potassium on both sides is about 1.3 at temperatures of 25° and 15° C. The ratio must be smaller at lower potassium concentrations and is 2.0 at 73.5 mM-K, which may be approaching the maximum value. 4. Although the oxygen uptake is independent of the K-transport, the reverse is not true. There is a close dependency of K-transport on oxygen consumption. 5. K-transport by the midgut contrasts with Na-transport by the frog skin because Na-transport stimulates oxidative metabolism whereas K-transport does not. Evidently the coupling of transport to energy supply is different in the two systems.

Dependence of the driving force of the sodium pump on rate of transport

1977 ◽  
Vol 232 (5) ◽  
pp. F448-F454
Author(s):  
Peter U. Feig ◽  
Gayle D. Wetzel ◽  
Howard S. Frazier
Keyword(s):  
Active Transport ◽  
Sodium Transport ◽  
Driving Force ◽  
Sodium Pump ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Base Line ◽  
Chemical Gradient ◽  
Electrical Analogue ◽  
Additional Support

The driving force for active transport of Na+ in the isolated toad bladder, ENa, was measured as the reciprocal slope of the change in conductance with change in short-circuit current after stimulation with antidiuretic hormone. The base-line short-circuit current was altered by change in ambient Na+ concentration or addition of amiloride, maneuvers which alter availability of Na+ at the site of active transport. In the absence of a chemical gradient for Na+ across the bladder, ENa was found to be inversely related to the rate of Na+ transport, a finding incompatible with the simple electrical analogue that has been proposed for the system. The results provide additional support for the view that ENa measured in this way has both energetic and kinetic components. membrane transport; active transport; sodium transport; ENa Submitted on April 23, 1976

Neurohypophyseal hormones and sodium transport

1971 ◽  
Vol 262 (842) ◽  
pp. 103-109 ◽  
Keyword(s):  
Active Transport ◽  
Sodium Transport ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Toad Bladder ◽  
Alternative View ◽  
General View ◽  
Ion Pump ◽  
Neurohypophyseal Hormones ◽  
Amphibian Epithelia

Neurohypophyseal hormones are known to affect the transfer characteristics of some amphibian epithelia to salt and water. The general view of sodium transport across toad bladder is that sodium enters the cells passively down a concentration gradient from the mucosal solution, and is pumped into the serosal solution by an unsaturated ion pump. Neurohypophyseal hormones are believed to stimulate transport by increasing the permeability of the mucosal surface to sodium ions. Measurements of the amount of sodium in the transport pool by tissue pool labelling has shown that the electrochemical gradient may not always be favourable for sodium entry across the mucosal border. Furthermore, other experiments have demonstrated that most of the labelled sodium pool, presumably intracellular, is beyond the active transport step. These difficulties have led to suggestions of alternative models for the active transport of sodium and for the actions of neurohypophyseal peptides. In this paper the effects of amiloride on short circuit current and sodium fluxes in isolated toad bladder is described, and an alternative view of the transport process is suggested.

11-Dehydrocorticosterone, a glucocorticoid metabolite, inhibits aldosterone action in toad bladder

1991 ◽  
Vol 261 (5) ◽  
pp. F873-F879 ◽  
Author(s):  
A. S. Brem ◽  
K. L. Matheson ◽  
J. L. Barnes ◽  
D. J. Morris
Keyword(s):  
Sodium Transport ◽  
Cell Layer ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Hydroxysteroid Dehydrogenase ◽  
Toad Bladder ◽  
Compound A ◽  
Dose Dependent Fashion ◽  
Epithelial Cell Layer ◽  
Dose Dependent

The enzyme 11 beta-hydroxysteroid dehydrogenase (11 beta-OHSD) metabolizes glucocorticoid hormones and diminishes their ability to induce sodium transport. In these studies, we determined the location of this enzyme in toad bladder and assessed the biological role for its 11-dehydro end product. Employing a polyclonal antibody directed toward 11 beta-OHSD and immunofluorescence techniques, we located the enzyme in the epithelial cell layer of the toad bladder. Although corticosterone (10(-7) M) can partially suppress aldosterone (10(-7) M)-stimulated short-circuit current (SCC), a clear excess of corticosterone (10(-6) M) did not inhibit the aldosterone-induced induced (10(-8) M) rise in SCC (n = 6). The 11-dehydro product of corticosterone, 11-dehydrocorticosterone (compound A) added to the serosal bath suppressed aldosterone (10(-8) M) peak SCC (360 min) in a dose-dependent fashion reaching 46 +/- 5% of control values at 10(-5) M (n = 6; P less than 0.001). Compound A (10(-5) M) in the mucosal bath also was capable of partially inhibiting the peak aldosterone rise in SCC to 63 +/- 7% of control values with aldosterone at 10(-8) M (n = 6; P less than 0.01) and to 64 +/- 10% of control values with aldosterone at 10(-7) M (n = 9; P less than 0.01). Compound A alone at 10(-5) M did not have any effect on SCC. Isolated toad bladders were not able to transform compound A (at 10(-8) and 10(-5) M) back to corticosterone. Thus the 11-dehydro end product of 11 beta-OHSD (compound A) may play a biologic role by regulating a component of mineralocorticoid-induced sodium transport.

Sodium transport by lamb proximal colon measured during early postnatal development

1982 ◽  
Vol 98 (1) ◽  
pp. 155-159 ◽  
Author(s):  
M. W. Smith ◽  
P. S. James
Keyword(s):  
Postnatal Development ◽  
Sodium Transport ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Proximal Colon ◽  
Early Postnatal Development ◽  
The Third ◽  
Electrolyte Absorption ◽  
Chloride Absorption

SUMMARYProximal colons taken from lambs up to 3 weeks after birth were shown to transport both sodium and chloride from lumen to blood when incubated in vitro.Sodium transport fell into three phases during postnatal development. The first covered the period from birth to 3 days of age when sodium transport was high and equal to that calculated from measurement of short-circuit current. The second was seen in 5- and 7-day-old lambs where the short-circuit current was low and the net transport of sodium was negligible. The third was seen in 2-3-week-old lambs where sodium transport was high, but the short-circuit current was low.Chloride absorption by colons taken from 1-day-old lambs appeared to be in exchange for an anion, possibly bicarbonate. Chloride absorption by colons taken from 3-week-old lambs appeared to be electrogenie or coupled directly to the transport of sodium.A possible explanation for the failure of electrolyte absorption by colons taken from 5- and 7-day-old lambs is discussed.

Active Transport by the Cecropia Midgut

1968 ◽  
Vol 48 (1) ◽  
pp. 1-12
Author(s):  
W. R. HARVEY ◽  
J. A. HASKELL ◽  
S. NEDERGAARD
Keyword(s):  
Transport Mechanism ◽  
Potassium Concentration ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Potassium Transport ◽  
Nernst Equation ◽  
Tissue Concentrations ◽  
Sodium Magnesium ◽  
Lines Of Evidence ◽  
Stimulation Of

1. From two lines of evidence, we conclude that the potassium transport gives rise directly to the midgut potential, i.e. that the active potassium transport mechanism is electrogenic. 2. First, diffusion potentials of neither potassium, sodium, magnesium, calcium, nor chloride could give rise to the large midgut potential if values for tissue concentrations are accepted for their respective activities in the epithelium. 3. Secondly, no externally added cation other than potassium is required to sustain either the potential or short circuit current, no specific anion is required, and no metabolic ion is known to be produced in sufficient amount to act as a counter ion for potassium in a non-electrogenic process. 4. Changes in the concentration of potassium on the blood-side of the midgut always lead to changes in potential in the direction predicted by the Nernst equation. Moreover, a tenfold change in potassium concentration leads to the expected 59 mV. potential change provided that the prior midgut potential is at least 130 mV. This effect could be attributed either to the stimulation of an electrogenic potassium pump or to a potassium diffusion potential across the blood-side barrier.

Aldosterone-stimulated transmethylations are linked to sodium transport

1985 ◽  
Vol 248 (1) ◽  
pp. F43-F47 ◽  
Author(s):  
W. P. Wiesmann ◽  
J. P. Johnson ◽  
G. A. Miura ◽  
P. K. Chaing
Keyword(s):  
Epithelial Cells ◽  
Sodium Transport ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Toad Bladder ◽  
Methylation Inhibitor ◽  
In Cells

The effect of aldosterone (Aldo) on phospholipid (PL) biosynthesis in cultured toad bladder epithelial cells was studied in cells incubated with [1,2-14C]choline and [methyl-3H]methionine over a 5-h period. Aldo (10(-7) M) did not alter the uptake of either precursor but significantly stimulated the incorporation of both labels into phosphatidylcholine (PC), the only PL labeled. 3H labeling of PC increased 29% and 14C incorporation into PC increased 34% in cells exposed to Aldo. A similar 30% increase in protein carboxymethylation occurred in cells treated with Aldo. 3-Deazaadenosine (DZA), a methylation inhibitor, abolished the Aldo-stimulated increase in PC labeling from [3H]methionine. PC labeling from [1,2-14C]choline was not affected by DZA. Basal and Aldo-stimulated protein carboxy-methylation were inhibited by DZA. DZA (300 microM) caused a mild decrease in basal short-circuit current (ISC) but completely inhibited the ISC response to 10(-7) M Aldo. Inhibition was complete when DZA was added up to 2 h following exposure to Aldo, and was reversible. Cells previously exposed to Aldo showed a significant increase in ISC within 2 h following removal of DZA. We conclude that Aldo stimulates PL methylation, protein carboxymethylation, and turnover of PC from choline. Inhibition of methylation reactions coincides with the inhibition of ISC response to Aldo.

Anterior pituitary control of active sodium transport across frog skin

1961 ◽  
Vol 200 (3) ◽  
pp. 444-450 ◽  
Author(s):  
R. M. Myers ◽  
W. R. Bishop ◽  
B. T. Scheer
Keyword(s):  
Sodium Transport ◽  
Rana Pipiens ◽  
Sodium Current ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Anterior Lobe ◽  
Sodium Ion ◽  
Resting Potential ◽  
Active Sodium ◽  
Active Sodium Transport

Removal of the anterior lobe of the pituitary from the frog Rana pipiens is followed by an increase in the outflux of Na22 across the skin, which persists at least 4 months, and by a decrease in resting potential and sodium (‘short-circuit’) current, which persists no more than 3 weeks. The increased outflux is interpreted as resulting from increased permeability of the skin to sodium ion, and the decreased sodium current is interpreted as a decreased rate of active sodium transport. Either change is opposed by treatment with mammalian ACTH or with aldosterone. Effects of other hormones could not be established with certainty. The increased permeability of the skin to sodium appears to be associated with a decrease in the amount of a mucopolysaccharide in the dermis. The evidence suggests that the pituitary effects involve the interrenal bodies.

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