Literature DB >> 1613483

Hemisodium, a novel selective Na ionophore. Effect on normal human erythrocytes.

D M Kaji1.   

Abstract

Hemisodium is a novel Na ionophore that belongs to the class of compounds called cryptands. These compounds possess an electron-rich cavity for binding of cations and are conformationally organized during synthesis to favor the selective binding of one cation over another. In media containing 145 mM NaCl and 5 mM KCl, hemisodium (10(-5) M) increased erythrocyte Na content from 23 to 345 mmol/kg.dry cell solid (dcs) over 4 h and increased water content from 1.8 to 3.5 liter/kg.dcs over the same period. K content decreased somewhat over the same time period, but this fall in K content was prevented entirely by incubation in either low Na media (to prevent net Na entry) or in Cl free media. Thus, the decrease in K content in high NaCl media was due to cell swelling, which activated KCl cotransport, and not due to a direct action of hemisodium on K permeability. Hemisodium-mediated Na transport was conductive, because erythrocyte membrane potential (Vm), determined by diS-C3-5 fluorescence, changed from -9 to +22 mV in high Na media in the presence of hemisodium and DIDS. In cells equilibrated with sulfamate, an anion with low conductive permeability, Vm changed 54 mV per 10-fold change in external Na concentration with the addition of hemisodium. In contrast, a 10-fold change in the external concentration of K, Rb, Cs, or T1 failed to alter Vm in the presence of hemisodium, suggesting a high Na specificity of the ionophore. Na conductance determined from net fluxes increased from 0.04 to 5.2 microS/cm2 with 10 microM hemisodium, and with that concentration the ratio of Na to K conductance was 45:1. Among the Na ionophores available so far, hemisodium appears to have the greatest specificity. Hemisodium may be a valuable tool in membrane transport studies.

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Year:  1992        PMID: 1613483      PMCID: PMC2216612          DOI: 10.1085/jgp.99.2.199

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  28 in total

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Authors:  A L HODGKIN; R D KEYNES
Journal:  J Physiol       Date:  1957-09-30       Impact factor: 5.182

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Authors:  J A Payne; C Lytle; T J McManus
Journal:  Am J Physiol       Date:  1990-11

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Authors:  A L HODGKIN; A F HUXLEY
Journal:  J Physiol       Date:  1952-04       Impact factor: 5.182

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Authors:  J A Halperin; C Brugnara; M T Tosteson; T Van Ha; D C Tosteson
Journal:  Am J Physiol       Date:  1989-11

5.  The effect of ATP, intracellular calcium and the anion exchange inhibitor DIDS on conductive anion fluxes across the human red cell membrane.

Authors:  P Bennekou; P Stampe
Journal:  Biochim Biophys Acta       Date:  1988-07-07

6.  Kinetics of volume-sensitive K transport in human erythrocytes: evidence for asymmetry.

Authors:  D M Kaji
Journal:  Am J Physiol       Date:  1989-06

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Authors:  D C Tosteson; T E Andreoli; M Tieffenberg; P Cook
Journal:  J Gen Physiol       Date:  1968-05       Impact factor: 4.086

8.  Voltage dependence of the Ca2+-activated K+ conductance of human red cell membranes is strongly dependent on the extracellular K+ concentration.

Authors:  B Vestergaard-Bogind; P Stampe; P Christophersen
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

9.  Effect of membrane potential on furosemide-inhibitable sodium influxes in human red blood cells.

Authors:  G R Kracke; P B Dunham
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

10.  The ion permeability induced in thin lipid membranes by the polyene antibiotics nystatin and amphotericin B.

Authors:  A Cass; A Finkelstein; V Krespi
Journal:  J Gen Physiol       Date:  1970-07       Impact factor: 4.086

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