Electron probe X-ray microanalysis of the effects of Bacillus thuringiensis var kurstaki crystal protein insecticide on ions in an electrogenic K+-transporting epithelium of the larval midgut in the lepidopteran, Manduca sexta, in vitro

1985 ◽  
Vol 74 (1) ◽  
pp. 137-152
Author(s):  
B.L. Gupta ◽  
J.A. Dow ◽  
T.A. Hall ◽  
W.R. Harvey
Keyword(s):  
Bacillus Thuringiensis ◽  
Manduca Sexta ◽  
Goblet Cell ◽  
Electron Probe ◽  
Apical Membrane ◽  
Short Circuit ◽  
Short Circuit Current ◽  
X Ray ◽  
Elemental Concentrations

An alkaline hydrolysate of Bacillus thuringiensis var kurstaki HD1 (Btk) parasporal crystals was administered at 25 micrograms ml-1 (f.c.) to isolated, short-circuited, midguts of tobacco hornworm (Manduca sexta) larvae. The short-circuit current (s.c.c.), a precise measure of K+ active transport, was inhibited by 78% in 10 min in Btk-treated midguts as compared to controls. The elemental concentrations of K, together with Na, Mg, P, S, Cl and Ca, as well as the water content, were determined by electron probe X-ray microanalysis (EPXMA) in the muscle cells, columnar cells and goblet cells, as well as in the extracellular goblet cavity and the bathing media. The average K concentration in the goblet cell cavity was 129 mmol/kg wet wt in control midguts but only 37 mmol/kg wet wt in Btk-treated midguts. The elemental concentrations, including that of K, in other cell compartments were much less affected by Btk, but a rise in total cell calcium is suggested. It has been previously suggested that in vitro Btk acts specifically on limited regions of the apical membrane of the midgut epithelial cells. The simplest interpretation of the EPXMA results would be that initially Btk interacts specifically with the goblet cell apical membrane, which bounds the goblet cavity and contains the K+ pump responsible for the s.c.c. and high transepithelial potential difference (p.d.). Such interaction results in a rapid disruption of K+ transport across the goblet cell apical membrane, leading to dissipation of the K+ gradient and loss of p.d. The histopathological changes previously reported by other workers would then be a consequence of K+ pump inhibition causing changes in the intracellular pH, Ca2+ etc. Some possible molecular bases for these specific interactions between Btk and cell membrane are discussed.

Comparison of Potassium Transport in Three Structurally Distinct Regions of The Insect Midgut

1981 ◽  
Vol 91 (1) ◽  
pp. 103-116
Author(s):  
MOIRA CIOFFI ◽  
WILLIAM R. HARVEY
Keyword(s):  
Goblet Cell ◽  
Apical Membrane ◽  
Close Association ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Potassium Transport ◽  
Structural Requirement ◽  
Posterior Midgut ◽  
New Information ◽  
Structural And Functional Properties

1. Active potassium transport across the isolated midgut of the Tobacco Hornworm larva, Manduca sexta, was studied by measuring the short circuit current (ISC) and unidirectional 42-potassium fluxes. 2. The midgut is composed of structurally distinct anterior, middle and posterior regions, all of which are shown to transport potassium, so that by comparing and contrasting their structural and functional properties new information on the mechanism of midgut potassium transport was obtained. 3. It has previously been shown that the potassium pump is located on the apical membrane of the goblet cell. In the anterior and middle regions of the midgut the goblet cell has a large cavity and mitochondria are closely associated with the apical membrane while in the posterior midgut the goblet cavity is much smaller, and mitochondria are not associated with the apical membrane. However, the apical membrane particles which have been implicated in active potassium transport in a number of other insect epithelia are present in all three regions. This observation suggests that the particles are a structural requirement for active transport, and that close association between mitochondria and the transporting membrane is not essential. 4. Comparison of the kinetic influx pool size and the differences in the ISC decay profiles between the three midgut regions suggest that part of the influx pool is a transported pool located in the goblet cavity. 5. A new model to explain the driving force for potassium transport in the midgut is proposed, in which the rate of potassium transport controls the entrance of potassium into the cell, rather than the opposite, currently accepted view.

Apical nonspecific cation conductances in rabbit cecum

1994 ◽  
Vol 266 (3) ◽  
pp. G475-G484 ◽  
Author(s):  
J. H. Sellin ◽  
W. P. Dubinsky
Keyword(s):  
Epithelial Transport ◽  
Apical Membrane ◽  
Divalent Cations ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Distal Colon ◽  
Na Channel ◽  
Similar Response ◽  
Electrogenic Transport

Rabbit cecum exhibits electrogenic Na absorption in vitro. However, because this transport process is not inhibited by amiloride nor does it demonstrate saturation kinetics typical of the amiloride-inhibitable Na channel, we considered whether the cecal transporter represented one of a recently described family of nonselective cation conductances or channels (NSCC). Both transepithelial and vesicle studies demonstrated that K, Cs, and Rb were transported via an apical conductance. Electrogenic transport was inhibited by divalent cations including Ca, Mg, and Ba but was unaffected by either lanthanum or gadolinium. Parallel studies in distal colon did not exhibit a similar response to either K substitution or Ba inhibition. Phenamil, verapamil, and nicardipine significantly inhibited the short-circuit current (Isc). stimulated by nominal Ca- and Mg-free conditions. Flux studies demonstrated a correlation between changes in Isc and Na transport. Microelectrode impalement studies suggested that there may be both NSCC and K conductance in the apical membrane. Planar bilayer studies identified a 190-pS cation channel that may correlate with the macroscopic transport properties of this epithelium. These studies are consistent with a model of cecal Na absorption mediated by a NSCC in the apical membrane; this may be the mechanism underlying the distinct epithelial transport characteristics of this intestinal segment.

L-glutamine with D-glucose stimulates oxidative metabolism and NaCl absorption in piglet jejunum

1992 ◽  
Vol 263 (6) ◽  
pp. G960-G966 ◽  
Author(s):  
J. M. Rhoads ◽  
E. O. Keku ◽  
J. P. Woodard ◽  
S. I. Bangdiwala ◽  
J. G. Lecce ◽  
...  
Keyword(s):  
Oxidative Metabolism ◽  
Carbonic Acid ◽  
Apical Membrane ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Glutamine Metabolism ◽  
Nacl Absorption ◽  
The Relationship ◽  
Stimulation Of

To explore the relationship between intestinal fluid absorption and oxidative metabolism, we measured the effects of amino acids and glucose on piglet jejunal ion transport and oxygen consumption (QO2) in vitro. Jejunal QO2 was stimulated by L-glutamine and D-glucose but not by the nonmetabolizable organic solutes methyl beta-D-glucoside or L-phenylalanine. QO2 was maximally enhanced by the combination of D-glucose and L-glutamine (5 mM). Even though 5 mM L-glutamine was previously found to be insufficient to stimulate NaCl absorption, 5 mM L-glutamine enhanced jejunal NaCl flux when combined with equimolar mucosal D-glucose. Either D-glucose or methyl beta-D-glucoside caused an increase in short-circuit current (Isc), an increase in Na+ absorption in excess of Isc, and a decrease in Cl- secretion, when L-glutamine was substituted for D-glucose (10 mM) on the serosal side. This relationship suggests that mucosal sugars, if combined with L-glutamine, enhance neutral NaCl absorption as well as electrogenic Na+ flow. (Aminooxy)acetate, an inhibitor of alanine aminotransferase, abolished the stimulation of QO2 and the NaCl-absorptive response to L-glutamine. We conclude that the oxidative metabolism fueled by L-glutamine is linked to a NaCl-absorptive mechanism in the intestine. We propose that the CO2 produced by glutamine metabolism yields carbonic acid, which dissociates to H+ and HCO3-, which may stimulate parallel antiports in the apical membrane.

Diluting segment in kidney of dogfish shark. II. Electrophysiology of apical membranes and cellular resistances

1990 ◽  
Vol 258 (2) ◽  
pp. R409-R417 ◽  
Author(s):  
S. C. Hebert ◽  
P. A. Friedman
Keyword(s):  
Apical Membrane ◽  
Short Circuit ◽  
Basolateral Membrane ◽  
Short Circuit Current ◽  
Membrane Resistance ◽  
Membrane Voltage ◽  
Primary Resistance ◽  
Diluting Segment ◽  
Dogfish Shark

Diluting segments from the bundle zone of the dogfish shark kidney were perfused in vitro and the electrophysiological characteristics of this segment investigated using conventional microelectrodes and cable analysis. In 21 tubules perfused with symmetrical Ringer solutions the average transepithelial voltage (Vte), transepithelial conductance (Gte), and equivalent short circuit current (Isc) were 8.7 +/- 0.6 mV, 91.3 +/- 10.2 mS/cm2, and 641 +/- 48 microA/cm2, respectively. Microelectrode impalements in 52 cells yielded values for the basolateral membrane voltage (Vb) and an estimated apical membrane fractional resistance (fRa) of -57.5 +/- 1.3 mV and 0.896 +/- 0.008, respectively. All of these parameters were distributed in a Gaussian manner. Liminal furosemide (10(-4) M) abolished Isc, hyperpolarized apical membrane voltage (Va) and Vb, increased Gte, and reduced fRa. The apical membrane was predominantly conductive to K+: increasing luminal K+ from 5 to 49.7 mM resulted in an apical depolarization of 41.2 mV and a fall in fRa and luminal Ba2+ (1 mM) depolarized Va by 14.3 mV and increased fRa. The apical transference number for K+ was 0.74 +/- 0.07. The cellular and paracellular resistances were estimated from the effects of luminal Ba2+ on fRa and Gte. The cell conductance represented approximately 45% of Gte, with the primary resistance barrier located at the apical membrane: apical membrane resistance was 59.7 +/- 16.0 and basolateral membrane resistance was 5.9 +/- 2.3 omega.cm2. From these resistance values together with the passive permeability (PNa/PCl) of 2.5 determined previously, the ratio of net Cl- absorption to net transcellular Na+ absorption was determined to be 2.(ABSTRACT TRUNCATED AT 250 WORDS)

Effect of loop diuretics on bullfrog cornea epithelium

1989 ◽  
Vol 256 (4) ◽  
pp. C750-C755 ◽  
Author(s):  
W. Nagel ◽  
G. Carrasquer
Keyword(s):  
Apical Membrane ◽  
Short Circuit ◽  
Membrane Conductance ◽  
Short Circuit Current ◽  
Loop Diuretics ◽  
Cl Transport ◽  
Before And After ◽  
The Difference ◽  
Cornea Epithelium

The effect of loop diuretics on Cl transport was studied on an in vitro preparation of the bullfrog cornea. Bumetanide (10(-4) M) or furosemide (10(-3) M) added to the stromal solution decreased Cl transport measured as the short-circuit current (Isc) to values near zero. Concomitantly, transepithelial conductance (gt) decreased, whereas the intracellular potential (Vo) hyperpolarized and the fractional resistance of the apical membrane (fRo) increased. Substitution of SO4 for Cl in the tear-side solution led to prompt changes in Isc, gt, Vo, and fRo, characteristic of appreciable passive Cl movement across the apical membrane before and after inhibition. Epinephrine (10(-4) M) was similarly effective on apical membrane conductance in inhibited tissues as under control conditions, but the effective electromotive force for transepithelial Cl transport was reduced to approximately 25%. Intracellular Cl activity, measured with ion-selective microelectrodes, decreased so much that the difference in electrochemical Cl potential divided by the Faraday constant (delta mu Cl/F) was close to zero after inhibition of Isc by bumetanide. Apical Cl permeability remained essentially unchanged. Accordingly, loop diuretics inhibit Cl transport in the Cl-secreting cornea epithelium by blocking the Na-Cl symport without secondary apical effects, as believed for other Cl-reabsorbing epithelia.

scholarly journals K+ CHANNEL PERMEATION AND BLOCK IN THE MIDGUT EPITHELIUM OF THE TOBACCO HORNWORM MANDUCA SEXTA

1994 ◽  
Vol 197 (1) ◽  
pp. 179-200
Author(s):  
K Schirmanns ◽  
W Zeiske
Keyword(s):  
Manduca Sexta ◽  
Short Circuit ◽  
Short Circuit Current ◽  
K Channel ◽  
K Channels ◽  
Zero Current ◽  
Channel Opening ◽  
Voltage Dependent ◽  
K Current

The K+-secreting larval midgut of Manduca sexta in vitro was voltage- or current-clamped. In contrast to Tl+, NH4+ and Na+, both Rb+ and K+ generated a short-circuit current, although with different saturation kinetics. The dependence of the short-circuit current on Rb+/K+ mole fraction gave no evidence for multi-ion occupation of the basolateral K+ channels. After 'functionally' eliminating the apical membranes using the ionophore amphotericin B and the 'apical K+ pump' blockers trimethyltin chloride or Tl+, the K+ channels could be more closely investigated. By measuring zero-current potentials, permeability ratios PX/PK were estimated using an adapted version of the Goldman­Hodgkin­Katz voltage equation. Their sequence was K+ (1) = Tl+ > Rb+ (0.38) > NH4+ (~0.3) > Cs+ (0.03) > Na+ (~0). The K+ channels could not be blocked by basally applied Cs+, Na+ or tetraethylammonium. Blockade of K+ current by Ba2+ was typically voltage-dependent, but only at moderate transbasal voltages. The relative electrical distance delta of the Ba2+ binding site from the basal channel opening was determined to be 0.2. At zero transbasal voltage, the apparent inhibition constant for barium KBa* was 1.7 mmol l-1.

Gene ablation for PEPT1 in mice abolishes the effects of dipeptides on small intestinal fluid absorption, short-circuit current, and intracellular pH

2010 ◽  
Vol 299 (1) ◽  
pp. G265-G274 ◽  
Author(s):  
Mingmin Chen ◽  
Anurag Singh ◽  
Fang Xiao ◽  
Ulrike Dringenberg ◽  
Jian Wang ◽  
...  
Keyword(s):  
Membrane Potential ◽  
Intracellular Ph ◽  
Fluid Transport ◽  
Apical Membrane ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Intestinal Fluid ◽  
Fluid Absorption

PEPT1 function in mouse intestine has not been assessed by means of electrophysiology and methods to assess its role in intracellular pH and fluid homeostasis. Therefore, the effects of the dipeptide glycilsarcosin (Gly-Sar) on jejunal fluid absorption and villous enterocyte intracellular pH (pHi) in vivo, as well as on enterocyte[14C]Gly-Sar uptake, short-circuit current ( Isc) response, and enterocyte pHi in vitro were determined in wild-type and PEPT1-deficient mice and in mice lacking PEPT1. Immunohistochemistry for PEPT1 failed to detect any protein in enterocyte apical membranes in Slc15a1−/− animals. Saturable Gly-Sar uptake in Slc15a1−/− everted sac preparations was no longer detectable. Similarly, Gly-Sar-induced jejunal Isc response in vitro was abolished. The dipeptide-induced increase in fluid absorption in vivo was also abolished in animals lacking PEPT1. Since PEPT1 acts as an acid loader in enterocytes, enterocyte pHi was measured in vivo by two-photon microscopy in SNARF-4-loaded villous enterocytes of exteriorized jejuni in anesthetized mice, as well as in BCECF-loaded enterocytes of microdissected jejunal villi. Gly-Sar-induced pHi decrease was no longer observed in the absence of PEPT1. A reversal of the proton gradient across the luminal membrane did not significantly diminish Gly-Sar-induced Isc response, whereas a depolarization of the apical membrane potential by high K+ or via Na+-K+-ATPase inhibition strongly diminished Gly-Sar-induced Isc responses. This study demonstrates for the first time that proton-coupled electrogenic dipeptide uptake in the native small intestine, mediated by PEPT1, relies on the negative apical membrane potential as the major driving force and contributes significantly to intestinal fluid transport.

scholarly journals AN INVESTIGATION OF THE MIDGUT K+ PUMP OF THE TOBACCO HORNWORM (MANDUCA SEXTA) USING SPECIFIC INHIBITORS AND AMPHOTERICIN B

1994 ◽  
Vol 188 (1) ◽  
pp. 191-204 ◽  
Author(s):  
K Schirmanns ◽  
W Zeiske
Keyword(s):  
Amphotericin B ◽  
Manduca Sexta ◽  
Short Circuit ◽  
Short Circuit Current ◽  
K Secretion ◽  
High Doses ◽  
Sites Of Action ◽  
Apical Membranes ◽  
Specific Inhibitors

Active K+ secretion in isolated posterior midguts of Manduca sexta was studied by measuring the short-circuit current. One aim of this study was to verify the postulate from biochemical reports that the cooperative apical arrangement of a vacuolar-type H+-ATPase (V-ATPase) and a K+/H+ antiporter drive the short-circuit current. Hence, we tested several specific inhibitors of the V-ATPase on the in vitro midgut preparation. Nitrate, bafilomycin A1, 7-chloro-4-nitrobenz-2-oxa-1,3-diazole (NBD-Cl) and amiloride all reduced the short-circuit current. This suggests that the H+-ATPase is involved in transepithelial K+ secretion. However, even at relatively high doses of these inhibitors, the block of the short-circuit current was not complete. Two other agents, thallium ions (Tl+, at millimolar concentrations) and trimethyltin chloride (TMT, 50 µmol l-1), did abolish the short-circuit current. Apical, but not basal, use of the ionophore amphotericin B largely eliminated the short-circuit current. This supports the view that the current-generating source resides in the apical membranes. An apical (and probably intracellular) site of action for NO3-, Tl+ and TMT is suggested by the observation that basal amphotericin B is needed for blockage by NO3- but does not, however, influence the effect of Tl+ and TMT. Likely sites of action are the V-ATPase (for nitrate and TMT) and the K+/H+ antiporter (for Tl+).

scholarly journals Temperature Acclimation of Intestinal Na Transport in the Carp (Cyprinus Carpio L.)

1985 ◽  
Vol 114 (1) ◽  
pp. 355-364
Author(s):  
J. S. Gibson ◽  
J. C. Ellory ◽  
A. R. Cossins
Keyword(s):  
Low Temperature ◽  
Apical Membrane ◽  
Short Circuit ◽  
Basolateral Membrane ◽  
Short Circuit Current ◽  
Temperature Acclimation ◽  
Na Transport ◽  
Carp Cyprinus Carpio ◽  
The Difference

1. Carp intestine mounted in vitro has a positive serosal potential and a net Na absorption greater than the short-circuit current. 2. At 30°C in vitro, tissues from 10°C-acclimated fish are thought to show heat-damage. 3. When measured at 10°C in vitro, intestine from fish acclimated to 10°C shows a greater rate of sodium transport than that from 30°Cacclimated fish. 4. Mucosal application of amphotericin B, at 10°C in vitro, increases short-circuit current and net Na flux in both 10°C- and 30°C-acclimated fish but does not diminish the difference in Na transport between the two groups, under conditions when the apical membrane permeability is not limiting. 5. It is concluded that the principal acclimatization in carp intestine to low temperature is via an increased basolateral membrane Na pumping capacity.

OSMOTIC INHIBITION OF THE NATRIFERIC RESPONSE OF THE TOAD URINARY BLADDER TO VASOPRESSIN

1975 ◽  
Vol 67 (1) ◽  
pp. 119-125
Author(s):  
P. J. BENTLEY
Keyword(s):  
Urinary Bladder ◽  
Water Movement ◽  
Short Circuit ◽  
Electrical Potential ◽  
Short Circuit Current ◽  
Toad Bladder ◽  
Toad Urinary Bladder ◽  
Electrical Potential Difference ◽  
Osmotic Gradient

SUMMARY The electrical potential difference and short-circuit current (scc, reflecting active transmural sodium transport) across the toad urinary bladder in vitro was unaffected by the presence of hypo-osmotic solutions bathing the mucosal (urinary) surface, providing that the transmural flow of water was small. Vasopressin increased the scc across the toad bladder (the natriferic response), but this stimulation was considerably reduced in the presence of a hypo-osmotic solution on the mucosal side, conditions under which water transfer across the membrane was also increased. This inhibition of the natriferic response did not depend on the direction of the water movement, for if the osmotic gradient was the opposite way to that which normally occurs, the response to vasopressin was still reduced. The natriferic response to cyclic AMP was also inhibited in the presence of an osmotic gradient. Aldosterone increased the scc and Na+ transport across the toad bladder but this response was not changed when an osmotic gradient was present. The physiological implications of these observations and the possible mechanisms involved are discussed.

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