Defining the volume dependence of multiple K flux pathways of trout red blood cells

1997 ◽  
Vol 272 (4) ◽  
pp. C1099-C1111 ◽  
Author(s):  
M. Berenbrink ◽  
Y. R. Weaver ◽  
A. R. Cossins

The volume sensitivity of different K flux pathways has been determined in trout red blood cells subjected to volume perturbation. Gentle hyposmotic swelling induced a K influx in a Cl-containing saline but not in NO3- or methanesulfonate (MeSF)-containing salines, consistent with the activation of a Cl-dependent flux. Extreme hyposmotic swelling led to larger K fluxes in all salines but with reduced anion discrimination of the Cl-dependent flux. In contrast to these graded responses, isosmotic swelling using ammonium chloride or beta-adrenergic stimulation activated only Cl-dependent fluxes in an all-or-none fashion. The relationship between the hyposmotically and isosmotically induced pathways was studied by coactivation using either ammonium chloride or isoproterenol with anisosmotic treatment. Cells in ammonium chloride-containing hyposmotic salines showed no additive K flux over that induced by hyposmotic treatment alone, indicating that the isosmotically induced Cl-dependent flux was identical to the hyposmotically induced Cl-dependent flux. However, cells coactivated by hyposmotic and beta-adrenergic treatment showed a small Cl-dependent flux in addition to that induced by hyposmotic treatment alone. This small third component was unaffected by anisosmotic treatment. We conclude that the major Cl-dependent and Cl-independent K flux pathways are distinct and separate and that the former has an anion dependence that varies with cell volume and a volume sensitivity that varies with ionic strength.

1990 ◽  
Vol 259 (5) ◽  
pp. C723-C726 ◽  
Author(s):  
A. Salama ◽  
M. Nikinmaa

We studied the effects of beta-adrenergic stimulation on the formation of adenosine 3',5'-cyclic monophosphate (cAMP) and on the cell volume in carp red blood cells in normoxia (PO2 = 150 mmHg) and hypoxia (PO2 = 8 mmHg). Accumulation of cAMP was the prerequisite for adrenergic cell swelling. Cell swelling was induced by beta-agonists, forskolin, and 8-bromo-cAMP. The amount of cAMP required for adrenergic swelling was minimal; swelling was observed at cAMP concentrations greater than 100 nM. Maximal increase in cell volume was observed at 200 nM cAMP. These values were independent of both the oxygen tension and the beta-agonist used. Norepinephrine caused the largest accumulation of cAMP, followed by isoproterenol and epinephrine. At hypoxic conditions, the cAMP concentrations obtained after stimulation with the natural catecholamines norepinephrine and epinephrine were greater than at normoxic conditions. The catecholamines caused appreciable cell swelling at lower concentrations in hypoxia than in normoxia. Thus the number of beta-adrenergic receptors, and their inherent ligand affinities, may be higher in hypoxic than in normoxic carp red blood cells. Oxygen tension had a pronounced effect on the magnitude of the adrenergic swelling. The maximal increase in cell volume was 5-7% in hypoxia, whereas in normoxia it was only approximately 2%. This was not due to differences in cAMP formation, but possibly to a greater activity of the Na(+)-H+ exchanger in hypoxic than in normoxic conditions.


2021 ◽  
Vol 2 (3) ◽  
pp. 139-168
Author(s):  
GF Fuhrmann ◽  
KJ Netter

This review article provides a critical survey of work from 1904 to 2003 on the effects of low ionic strength in Red Blood Cells (RBCs) incubated in media with impermeable sugars such as sucrose. In 1904 Gürber A washed RBCs of different species with isotonic sucrose solution to eliminate the outside ions in order to better analyse their intracellular ionic composition; however, this approach was not feasible because of a substantial salt efflux from the cells. A prominent feature of the salt loss is the shrinking of the RBCs. A central role in the understanding of the ionic movements is thereby the new Donnan equilibrium of the anions. Experimental evidence has been given by Jacobs MH and Parpart AK in 1933. In the sucrose medium two phases could be predicted: 1) a very rapid anionic shift resulting in an unequal distribution of chloride and hydroxyl anions on both sides of the membrane and 2) a leakage of salts from the RBCs. In 1940 Wilbrandt W assumed that a positive membrane potential is in line with the salt loss at low ionic strength in RBCs. In 1977 Knauf PA, Fuhrmann GF, Rothstein S and Rothstein A observed in RBCs an inhibition of both, anion exchange and also of net anion efflux, by incubation with disulfonic stilbene derivates. At low ionic strength the Donnan equilibrium is immediately obtained by the Anion Exchanger Protein (AEP). The resulting positive membrane potential opens at least two new types of cation pores or channels. Thereby is the conductivity pathway for the anions, namely the AEP, in charge of the net anion loss at low ionic strength. The AEP pathway is extensively blocked by disulfonic stilbene compounds. The permeability ways for cations through these pores or channels are not yet explored.


1989 ◽  
Vol 257 (1) ◽  
pp. C114-C121 ◽  
Author(s):  
N. al-Rohil ◽  
M. L. Jennings

In this study the volume-dependent or N-ethylmaleimide (NEM)-stimulated, ouabain-insensitive K+ influx and efflux were measured with the tracer 86Rb+ in rabbit red blood cells. The purpose of the work was to examine the rabbit as a potential model for cell volume regulation in human SS red blood cells and also to investigate the relationship between the NEM-reactive sulfhydryl group(s) and the signal by which cell swelling activates the transport. Ouabain-resistant K+ efflux and influx increase nearly threefold in cells swollen hypotonically by 15%. Pretreatment with 2 mM NEM stimulates efflux 5-fold and influx 10-fold (each measured in an isotonic medium). The ouabain-resistant K+ efflux was dependent on the major anion in the medium. The anion dependence of K+ efflux in swollen or NEM-stimulated cells was as follows: Br- greater than Cl- much greater than NO3- = acetate. The magnitudes of both the swelling- and the NEM-stimulated fluxes are much higher in young cells (density separated but excluding reticulocytes) than in older cells. Swelling- or NEM-stimulated K+ efflux in rabbit red blood cells was inhibited 50% by 1 mM furosemide, and the inhibitory potency of furosemide was enhanced by extracellular K+, as is known to be true for human AA and low-K+ sheep red blood cells. The swelling-stimulated flux in both rabbit and human SS cells has a pH optimum at approximately 7.4. We conclude that rabbit red blood cells are a good model for swelling-stimulated K+ transport in human SS cells.(ABSTRACT TRUNCATED AT 250 WORDS)


1979 ◽  
Vol 73 (1) ◽  
pp. 61-71 ◽  
Author(s):  
V Castranova ◽  
J F Hoffman

After incubation in isotonic KCl, dog red blood cells can be separated by centrifugation into subgroups which assume different cell volumes and possess different transport characteristics. Those red cells which swell in isotonic KCl exhibit a higher permeability to K and possess a greater volume dependence for transport of K than those red cells which shrink. A high Na permeability characterizes cells which shrink in isotonic KCl and these cells exhibit a larger volume-dependent Na flux than those red cells which swell. These two subgroups of red cells do not seem to represent two cell populations of different age. The results indicate that the population of normal cells is evidently heterogeneous in that the volume-dependent changes in Na and K permeability are distributed between differnt cell types rather than representing a single cell type which reciprocally changes its selectivity to Na and K.


2009 ◽  
Vol 5 (2) ◽  
pp. 95-104 ◽  
Author(s):  
B. A. Rasmusen ◽  
Elizabeth M. Tucker ◽  
J. C. Ellory ◽  
R. L. Spooner

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