Na+-K+-ATPase and Na+/Ca2+exchange activities in gills of hyperregulatingCarcinus maenas

1999 ◽  
Vol 276 (2) ◽  
pp. R490-R499 ◽  
Author(s):  
Čedomil Lucu ◽  
Gert Flik
Keyword(s):  
Atpase Activity ◽  
Specific Activity ◽  
Short Circuit ◽  
Carcinus Maenas ◽  
High Capacity ◽  
Short Circuit Current ◽  
Total Activity ◽  
Camp Content ◽  
Dependent Protein ◽  
Leaky Epithelium

Na+-K+-ATPase and Na+/Ca2+exchange activities were studied in gills of Carcinus maenas in seawater (SW) and after transfer to dilute seawater (DSW). Carcinushyperregulates its hemolymph osmolarity through active uptake of Na+, Cl−, and Ca2+. In DSW total Na+-K+-ATPase activity in posterior gills quadrupled; Na+/Ca2+exchange specific activity was unaffected, and total activity increased 1.67-fold. Short-circuit current ( Isc) in voltage-clamped posterior gill hemilamellae was −181 μA/cm2in SW and −290 μA/cm2in DSW and up to 90% ouabain sensitive; conductivity was similar in SW or DSW (42 and 46 mS/cm2, respectively) and representative of a leaky epithelium. The new steady state of hemolymph osmolarity 24 h after DSW transfer was preceded, already 3 h after transfer, by increased Na+-K+-ATPase but not Na+/Ca2+exchange activity. Western blot analysis indicated that the amount of Na+-K+-ATPase protein had increased 2.1-fold in crabs acclimated 3 wk to DSW; however, 4 h after DSW transfer no difference in the amount of Na+-K+-ATPase protein was observed. After DSW transfer branchial cAMP content decreased. A negative correlation between branchial Na+-K+-ATPase activity and cAMP content points to rapid regulation of Na+-K+-ATPase through cAMP-dependent protein kinase A activity. Ca2+transport may depend on the high-capacity Na+/Ca2+exchanger coupled to the versatile sodium pump.

scholarly journals A V-ATPase drives active, electrogenic and Na+-independent Cl- absorption across the gills of Eriocheir sinensis

1995 ◽  
Vol 198 (3) ◽  
pp. 767-774 ◽  
Author(s):  
H Onken ◽  
M Putzenlechner
Keyword(s):  
Atpase Activity ◽  
Specific Activity ◽  
Short Circuit ◽  
Specific Inhibitor ◽  
Membrane Vesicles ◽  
Short Circuit Current ◽  
Eriocheir Sinensis ◽  
Similar Distribution ◽  
Fluorescence Studies ◽  
F1fo Atpase

Using biochemical and electrophysiological techniques, we have examined the proposal that an H+-ATPase is involved in Cl- uptake across the gills of the Chinese crab Eriocheir sinensis. Bafilomycin A1 (1 µmol l-1), a specific inhibitor of V-ATPases, was used to investigate the importance of this H+-translocating enzyme in Cl- transport across the gill. In homogenates of ion-transporting posterior gills, we found the activity of a bafilomycin-sensitive V-ATPase to be markedly higher than in the anterior gills, which are not involved in ion transport. A similar distribution was found for the Na+/K+- and the mitochondrial F1Fo-ATPase. After differential and density centrifugation, the specific activity of the V-ATPase was enriched by a factor of 5. Neither Na+/K+- and F1Fo-ATPase activities nor acid phosphatase activity copurified with the bafilomycin-sensitive ATPase activity, indicating that at least the major portion of V-ATPase activity is not of basolateral, mitochondrial or lysosomal origin. In fluorescence studies, using Acridine Orange or Oxonol V as dyes, membrane vesicles displayed ATP-dependent proton transport and membrane potential generation, which were markedly reduced in the presence of bafilomycin. In addition to these biochemical studies, we mounted split lamellae of posterior gills in an Ussing-type chamber and measured the negative short-circuit current (Isc), which was shown to reflect active, electrogenic, Na+-independent and ouabain-insensitive Cl- absorption. After the addition of 1 µmol l-1 bafilomycin to the external bath, this Isc was reduced to about 50­60 % of its original value. Concomitantly, the conductance of the preparation decreased by about 13 %. From these results, we conclude that an apical V-ATPase drives electrogenic Cl- uptake across the posterior gills of the Chinese crab.

Regulation of ion transport in porcine gallbladder: effects of VIP and norepinephrine

1989 ◽  
Vol 257 (1) ◽  
pp. C52-C57 ◽  
Author(s):  
S. M. O'Grady ◽  
P. J. Wolters ◽  
K. Hildebrand ◽  
D. R. Brown
Keyword(s):  
Receptor Antagonist ◽  
Adrenergic Receptor ◽  
Sulfonic Acid ◽  
Short Circuit ◽  
Fold Increase ◽  
Short Circuit Current ◽  
Maximal Effect ◽  
Camp Content ◽  
Flux Measurements

The objective of this study was to investigate the effects of vasoactive intestinal peptide (VIP) and norepinephrine (NE) on Na and Cl transport across the isolated porcine gallbladder. Serosal addition of either VIP or secretin increased the short-circuit current (Isc). The half-maximal effect for VIP was 84.3 nM. The effect of VIP was mimicked by 8-bromoadenosine 3',5'-cyclic monophosphate (8-BrcAMP). Replacement of Cl with gluconate nearly abolished the effect of 8-BrcAMP on Isc, whereas HCO3 replacement with N-2-hydroxyethylpiperazine-N'-2-ethane-sulfonic acid buffer had no effect. Transepithelial flux measurements indicated that 8-BrcAMP stimulates net Cl secretion and inhibits Na absorption. Norepinephrine inhibits VIP-stimulated changes in Isc as well as the basal Isc. NE does not, however, reverse the effects of 8-BrcAMP on Isc. The effects of NE are antagonized by yohimbine (alpha 2-adrenergic receptor antagonist) but not prazosin (an alpha 1-adrenergic receptor antagonist). VIP causes a 2.5-fold increase in cAMP content in the gallbladder epithelium. This increase is blocked by NE. Serosal tetrodotoxin did not inhibit the peptide effects, indicating that VIP receptors are localized on the epithelium. Depolarization of submucosal nerves with veratrine inhibited the basal Isc and was reversible with yohimbine. This result indicated that sympathetic nerve pathways regulate Na and Cl absorption in vitro.

Hormonal regulation of Na+-K+-ATPase in cultured epithelial cells

1986 ◽  
Vol 251 (2) ◽  
pp. C186-C190 ◽  
Author(s):  
J. P. Johnson ◽  
D. Jones ◽  
W. P. Wiesmann
Keyword(s):  
Enzyme Activity ◽  
Epithelial Cells ◽  
Atpase Activity ◽  
Hormonal Regulation ◽  
Short Circuit ◽  
Short Circuit Current ◽  
Toad Urinary Bladder ◽  
A6 Cells ◽  
Cultured Epithelial Cells ◽  
Stimulation Of

Aldosterone and insulin stimulate Na+ transport through mechanisms involving protein synthesis. Na+-K+-ATPase has been implicated in the action of both hormones. We examined the effect of aldosterone and insulin on Na+-K+-ATPase in epithelial cells in culture derived from toad urinary bladder (TB6C) and toad kidney (A6). Aldosterone, but not insulin, increases short-circuit current (ISC) in TB6C cells. Aldosterone increases Na+-K+-ATPase activity after 18 h of incubation, but no effect can be seen at 3 and 6 h. Amiloride, which inhibits aldosterone-induced increases in ISC, has no effect on either basal or aldosterone stimulated enzyme activity. Both aldosterone and insulin increase ISC in A6 cells and when added together are synergistic. Aldosterone stimulates enzyme activity in A6 cells, but insulin alone has no effect. However, aldosterone and insulin together stimulate enzyme activity more than aldosterone alone. It appears that stimulation of Na+-K+-ATPase activity is involved in aldosterone action in both cell lines but does not appear to be due to increased Na+ entry, since enhanced enzyme activity is not inhibited by amiloride. In contrast, insulin alone has no direct effect on Na+-K+-ATPase, although the increased enzyme activity following both agents in combination may explain their synergism on ISC.

Ileal mucosal cyclic AMP and Cl secretion: serosal vs. mucosal addition of cholera toxin.

1977 ◽  
Vol 232 (2) ◽  
pp. E210 ◽  
Author(s):  
H E Sheerin ◽  
M Field
Keyword(s):  
Cyclic Amp ◽  
Ion Transport ◽  
Cholera Toxin ◽  
Short Circuit ◽  
Electrical Conductance ◽  
Short Circuit Current ◽  
Serosal Side ◽  
Ileal Mucosa ◽  
Camp Content ◽  
Mucosal Side

Changes in ion transport and cyclic AMP (cAMP) concentration produced by addition of cholera toxin to the serosal side of isolated rabbit ileal mucosa (CTs) were compared to the changes produced by addition to the mucosal side (CTm). CTs increased short-circuit current (SCC) as did CTm but it did so more slowly. CTs, unlike CTm, did not significantly decrease electrical conductance. Inhibition of the SCC response to theophylline, a measure of preexisting secretion, was almost complete 180 min after CTm but was not yet significant 180 min after CTs. Longer (280 min) after CTs, the SCC response to theophylline was reduced by 59%, a significant reduction but less than that caused by CTm. A statistically significant change in net Cl flux could not be demonstrated after CTs, although at 280 min the measured flux was halfway between the fluxes for control and CTm tissues. Cyclic AMP concentrations were determined at 190 min, 10 min after addition of theophylline. CTs, despite little or no effect on ion transport, increased cAMP to the same level as did CTm, and the effect on cAMP of adding toxin to both sides was additive. We conclude that 1) active secretion is probably stimulated by cholera toxin added on the serosal side, although more slowly than after addition to the mucosal side and 2) much of the toxin-stimulated cAMP content of the mucosa is not coupled to secretion.

Characterization of Na-K-ATPase in dog tracheal epithelium: enzymatic and ion transport measurements

1980 ◽  
Vol 48 (6) ◽  
pp. 1008-1019 ◽  
Author(s):  
C. Westenfelder ◽  
W. R. Earnest ◽  
F. Al-Bazzaz
Keyword(s):  
Atpase Activity ◽  
Ethacrynic Acid ◽  
Specific Activity ◽  
Short Circuit ◽  
High Specific Activity ◽  
Tracheal Epithelium ◽  
Bathing Solution ◽  
Tracheal Mucosa ◽  
Ussing Chambers ◽  
Cl Secretion

The dog tracheal epithelium actively secretes Cl and absorbs Na. The possible dependency of this electrolyte transport on a Mg-dependent, Na-K-activated adenosine triphosphatase (Na-K-ATPase, EC 3.6.1.3) was examined. The characteristics of this enzyme system were investigated using homogenates of tracheal epithelium. The electrical properties and ion fluxes of this epithelium were determined in tissues mounted in Ussing chambers. Addition of Na and K produced an approximate 50% activation of basal Mg-ATPase activity. The apparent Km values for ATP, Na, K, and Mg were 0.4, 12.7, 1.9, and 1.6 mM, respectively. The total specific ATPase activity was 8.1 ± 0.4 and that of the Mg-ATPase 4.3 ± 0.1 mumol Pi. mg protein -1.h-1. Addition of ouabain (1 muM) or omission of K from the submucosal bathing solution reduced potential difference (PD) and short-circuit current (SCC) significantly. Relatively low concentrations (0.1 mM or less) of ethacrynic acid, furosemide, or 2,4-dinitrophenol (2,4-DNP) depressed SCC and PD significantly, i.e., at concentrations that were without effect on the Na-K-ATPase activity. Ethacrynic acid inhibited Cl secretion, whereas 2,4-DNP lowered both Na and Cl transport. These data demonstrate that 1) the tracheal mucosa of dogs contains a Na-K-ATPase at relatively high specific activity, 2) this enzyme is likely contained in the basal aspect of this membrane, 3) it appears to be essential for maintenance of Cl secretion, and 4) Cl secretion can be reduced (by ethacrynic acid, furosemide, and 2,4-DNP) without Na-K-ATPase inhibition.

Active ammonia excretion across the gills of the green shore crabCarcinus maenas: participation of Na+/K+-ATPase, V-type H+-ATPase and functional microtubules

2002 ◽  
Vol 205 (18) ◽  
pp. 2765-2775 ◽  
Author(s):  
Dirk Weihrauch ◽  
Andreas Ziegler ◽  
Dietrich Siebers ◽  
David W. Towle
Keyword(s):  
Short Circuit ◽  
Basolateral Membrane ◽  
Carcinus Maenas ◽  
Specific Inhibitor ◽  
Ammonia Excretion ◽  
Short Circuit Current ◽  
Shore Crab ◽  
Dependent Manner ◽  
Microtubule Network ◽  
Experimental Conditions

SUMMARYAlthough aquatic animals are generally believed to export nitrogenous waste by diffusion of NH3 or NH4+ across external epithelia, evidence for active ammonia excretion has been found in a number of species. In the euryhaline green shore crab Carcinus maenas, active excretion of ammonia across isolated gills is reduced by inhibitors of the Na+/K+-ATPase and vacuolar-type H+-ATPase. In addition, a functional dynamic microtubule network is necessary, since application of colchicine, taxol or thiabendazole leads to almost complete blockage of active and gradient-driven ammonia excretion. Actin filaments seem not to play a role in the excretory process. The NH4+-dependent short-circuit current and the conductance of the isolated cuticle were reduced in a dose-dependent manner by amiloride,a non-specific inhibitor of the Na+/H+ exchanger and Na+ channels. Combined with an analysis of gill morphology, the strong intracellular but weak apical abundance of V-type H+-ATPase and the fact that ammonia flux rates are equal under buffered and unbuffered experimental conditions, our observations suggest a hypothetical model of transepithelial ammonia movement that features active uptake across the basolateral membrane, sequestration in acidified vesicles, vesicle transport via microtubules and exocytosis at the apical membrane.

Activation of CFTR by ASBT-mediated bile salt absorption

2005 ◽  
Vol 289 (5) ◽  
pp. G870-G879 ◽  
Author(s):  
Marcel J. C. Bijvelds ◽  
Huub Jorna ◽  
Henkjan J. Verkade ◽  
Alice G. M. Bot ◽  
Franz Hofmann ◽  
...  
Keyword(s):  
Protein Kinase ◽  
Bile Salt ◽  
Kinase Inhibitor ◽  
Short Circuit ◽  
Basolateral Membrane ◽  
Anion Channel ◽  
Short Circuit Current ◽  
Distal Ileum ◽  
Dependent Protein Kinase ◽  
Dependent Protein

In cholangiocytes, bile salt (BS) uptake via the apical sodium-dependent bile acid transporter (ASBT) may evoke ductular flow by enhancing cAMP-mediated signaling to the cystic fibrosis transmembrane conductance regulator (CFTR) anion channel. We considered that ASBT-mediated BS uptake in the distal ileum might also modulate intestinal fluid secretion. Taurocholate (TC) induced a biphasic rise in the short circuit current across ileal tissue, reflecting transepithelial electrogenic ion transport. This response was sensitive to bumetanide and largely abrogated in Cftr-null mice, indicating that it predominantly reflects CFTR-mediated Cl−secretion. The residual response in Cftr-null mice could be attributed to electrogenic ASBT activity, as it matched the TC-coupled absorptive Na+flux. TC-evoked Cl−secretion required ASBT-mediated TC uptake, because it was blocked by a selective ASBT inhibitor and was restricted to the distal ileum. Suppression of neurotransmitter or prostaglandin release, blocking of the histamine H1receptor, or pretreatment with 5-hydroxytryptamine did not abrogate the TC response, suggesting that neurocrine or immune mediators of Cl−secretion are not involved. Responses to TC were retained after carbachol treatment and after permeabilization of the basolateral membrane with nystatin, indicating that BS modulate CFTR channel gating rather than the driving force for Cl−exit. TC-induced Cl−secretion was maintained in cGMP-dependent protein kinase II-deficient mice and only partially inhibited by the cAMP-dependent protein kinase inhibitor H89, suggesting a mechanism of CFTR activation different from cAMP or cGMP signaling. We conclude that active BS absorption in the ileum triggers CFTR activation and, consequently, local salt and water secretion, which may serve to prevent intestinal obstruction in the postprandial state.

High Capacity High-Speed Switch Application Analysis and Action Process Simulation

2015 ◽  
Vol 1092-1093 ◽  
pp. 276-280
Author(s):  
Tie Ying Zhao ◽  
Jun Ling Liu
Keyword(s):  
High Speed ◽  
Short Circuit ◽  
High Capacity ◽  
Short Circuit Current ◽  
Current Level ◽  
Parallel Structure ◽  
Application Analysis ◽  
Current Limiting ◽  
Simulation Results ◽  
Action Process

This paper analyzed high capacity high speed switch’s works and structures, proposed a parallel structure of high capacity high speed switch (FSR) with current limiting reactor. Through analysis of its action process, this paper used EMTP/ATP to simulate FSR action process, analyzed line current and voltage changes in normal and short circuit station. Simulation results show that the method can effectively limit short circuit current level.

scholarly journals Naringenin Regulates CFTR Activation and Expression in Airway Epithelial Cells

2017 ◽  
Vol 44 (3) ◽  
pp. 1146-1160 ◽  
Author(s):  
Rui Shi ◽  
Zi-Ting Xiao ◽  
Yi-Jun Zheng ◽  
Yi-Lin Zhang ◽  
Jia-Wen Xu ◽  
...  
Keyword(s):  
Epithelial Cells ◽  
Short Circuit ◽  
Short Circuit Current ◽  
The Elderly ◽  
Airway Epithelial Cells ◽  
Intracellular Camp ◽  
Transmembrane Conductance Regulator ◽  
Airway Epithelial ◽  
Camp Content ◽  
Basolateral Side

Background/Aims: Sputum symptoms are commonly seen in the elderly. This study aimed to identify an efficacious expectorant treatment stratagem through evaluating the secretion-promoting activation and cystic fibrosis transmembrane conductance regulator (CFTR) expression of the bioactive herbal monomer naringenin. Methods: Vectorial Cl- transport was determined by measuring short-circuit current (ISC) in rat airway epithelium. cAMP content was measured by ELISA in primary cultured epithelial cells and Calu-3 cells. CFTR expression in Calu-3 cells was determined by qPCR. Results: Addition of naringenin to the basolateral side of the rat airway led to a concentration-dependent sustained increase in ISC. The current was suppressed when exposed to Cl–-free solution or by bumetanide, BaCl2, and DPC but not by DIDS and IBMX. Forskolin-induced ISC increase and CFTRinh-172/MDL-12330A-induced ISC inhibition were not altered by naringenin. Intracellular cAMP content was significantly increased by naringenin. With lipopolysaccharide stimulation, CFTR expression was significantly reduced, and naringenin dose-dependently enhanced CFTR mRNA expression. Conclusion: These results demonstrate that naringenin has the ability to stimulate Cl- secretion, which is mediated by CFTR through a signaling pathway by increasing cAMP content. Moreover, naringenin can increase CFTR expression when organism CFTR expression is seriously hampered. Our data suggest a potentially effective treatment strategy for sputum.

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