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Query: UMLS:C0027960 (mole)
 21,279 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

1. The steady-state tracer exchange flux of chloride was measured at 10-150 mM external chloride concentration, substituting either lactate or sucrose for chloride. The chloride flux saturates in both cases with a K 1/2 about 50 and 15 mM, respectively. 2. The inhibitory effect of other monovalent anions on the chloride transport was investigated by measuring the 36Cl- efflux into media where either bromide, nitrate, or thiocyanate had been substituted for part of the chloride. The sequence of increasing affinity for the chloride transport system was found to be: Br- less than Cl- less than SCN- = NO3-. 3. The chloride steady-state exchange flux in the presence of nitrate can be described by Michaelis-Menten kinetics with nitrate as a competitive inhibitor of the chloride flux. 4. The apparent activation energy (EA) was determined to be 67 +/- 6.2 kJ/mole, and was constant between 7 and 38 degrees C. 5. The membrane potential (Vm) was measured as a function of the concentration of external K+, substituting K+ for Na+. The transference number of K+ (tK) was estimated from the slope of Vm vs. log10 (K+)e, and tCl and tNa were calculated, neglecting current carried by ions other than Cl-, K+, and Na+. The diffusional net flux of K+ was calculated from the steady-state exchange flux of 42K+, assuming the flux ratio equation to be valid. From this value the K+ conductance and the Na+ and Cl- conductances were calculated. The experiments showed that GCl, GNa, and GK are all about 14 muS/cm2. 6. The net (conductive) chloride permeability derived from the chloride conductance was 4 x 10(-8) cm/sec compared with the apparent permeability of 6 x 10(-7) cm/sec as calculated from the chloride tracer exchange flux. These data suggest that about 95% of the chloride transport is mediated by an electrically silent exchange diffusion. 7. Comparable effects of phloretin (0.25 mM) on the net (conductive) permeability and the apparent permeability to chloride (about 80% inhibition) may indicate that the chloride exchange and conductance pathways are not completely separate and distinct modes of transport, but may involve common elements. The reduced chloride permeability in the presence of phloretin is estimated to be two orders of magnitude larger than the ground permeability of the cell membrane.
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PMID:Membrane potential, chloride exchange, and chloride conductance in Ehrlich mouse ascites tumour cells. 52 33

The lactoperoxidase-catalyzed oxidation of glutathione (GSH) and thiocyanate (SCN-) was studied. Oxidation of SCN- was recorded by ultraviolet spectroscopy and by electron spin resonance (ESR). Consumption of GSH was measured by amperometric titration. One or two moles of GSH was oxidized per mole of H2O2 added, depending on the reaction conditions. Omission of SCN- prevented the oxidation of GSH. The oxidation of GSH required only catalytic amounts of SCN-, which was therefore recycled. Iodide (I-) could replace SCN-, while chloride or bromide were ineffective. The apparent Michaelis constant for SCN- was 17 microM. Oxidation of SCN- gave rise to two reactive intermediates, one stable and one unstable. The stable intermediate (-OSC. = N-(?)) decayed by a second-order reaction with a rate constant of 1.1 M-1 s-1. The decay of the unstable radical was very fast. The data (a) explain the short- and long-term antibacterial effects of lactoperoxidase-halide-H2O2 system, (b) point to possible deleterious effects due to glutathione depletion, (c) are of relevance for free radical diseases involving sulphur-centered free radicals, and (d) support previous observations on lipid peroxidation/halogenation in biological membranes, liposomes, and unsaturated fatty acids.
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PMID:Free radical generation and coupled thiol oxidation by lactoperoxidase/SCN-/H2O2. 132 2

Single channel currents though apical membrane Cl channels of the secretory epithelial cell line T84 were measured to determine the anionic selectivity and concentration dependence of permeation. The current-voltage relation was rectified with single channel conductance increasing at positive potentials. At 0 mV the single channel conductance was 41 +/- 2 pS. Permeability, determined from reversal potentials, was optimal for anions with diameters between 0.4 and 0.5 nm. Anions of larger diameter had low permeability, consistent with a minimum pore diameter of 0.55 nm. Permeability for anions of similar size was largest for those ions with a more symmetrical charge distribution. Both HCO3 and H2PO4 had lower permeability than the similar-sized symmetrical anions, NO3 and ClO4. The permeability sequence was SCN greater than I approximately NO3 approximately ClO4 greater than Br greater than Cl greater than PF6 greater than HCO3 approximately F much greater than H2PO4. Highly permeant anions had lower relative single channel conductance, consistent with longer times of residence in the channel for these ions. The conductance sequence for anion efflux was NO3 greater than SCN approximately ClO4 greater than Cl approximately I approximately Br greater than PF6 greater than F approximately HCO3 much greater than H2PO4. At high internal concentrations, anions with low permeability and conductance reduced Cl influx consistent with block of the pore. The dependence of current on Cl concentration indicated that Cl can also occupy the channel long enough to limit current flow. Interaction of Cl and SCN within the conduction pathway is supported by the presence of a minimum in the conductance vs. mole fraction relation. These results indicate that this 40-pS Cl channel behaves as a multi-ion pathway in which other permeant anions could alter Cl flow across the apical membrane.
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PMID:Anion permeation in an apical membrane chloride channel of a secretory epithelial cell. 137 74

Bi-ionic membrane potential measurements and three-microelectrode voltage clamp experiments have been performed on surface fibres of Xenopus laevis sartorius muscle at various mole fractions of SCN- in Cl- in the perfusate, at pH 5. Potassium was replaced in the test solutions by rubidium and/or tetraethylammonium and when the mole fraction of anions was changed the measured membrane potential changed to a new constant (i.e. time-independent) value. Over a mole fraction range of 0.05-0.95 the permeability ratio of thiocyanate to chloride was independent of [SCN-]. When the bathing solution was completely changed from control to one containing thiocyanate the change in membrane potential indicated that the permeability ratio, PSCN/PCl is close to 5.9. Inward voltage clamp currents (chloride efflux) were suppressed in the presence of thiocyanate, the degree of suppression increasing with [SCN-]. Outward currents (anion influx) were not substantially altered, suggesting that it is only the voltage-dependent anion current that is sensitive to SCN-. The results are interpreted as indicating that there is a binding site in the anion-conducting channel, accessible to the extracellular space, that must be occupied by an anion in order for the channel to be "open". But that for ion traverse to be complete, the ion at the binding site must be exchanged. If the site is occupied by thiocyanate, the more strongly bound ion, the thiocyanate blocks the channel. The bi-ionic permeability ratio is thought to reflect the ratio of the binding constants for the anions at that site.
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PMID:Chloride-thiocyanate interactions in frog muscle anion-conducting channels at pH 5. 244 45

1. Multiple conductance level ion channels were recorded in excised and cell-attached patches from cells of a mouse B lymphocyte hybridoma line. The reversal potential for the single-channel current was unaffected by the species of cation on the cytoplasmic face of the patch, but changed as the Cl- concentration was altered, indicating that the channel is anion selective. 2. The permeability sequence determined from reversal potentials was F- greater than I- greater than SCN- greater than Br- greater than Cl- greater than glucuronate greater than NO3- greater than aspartate. This was different from the conductance sequence (Cl- greater than SCN- = F- greater than Br- greater than NO3- greater than I- greater than glucuronate greater than aspartate), indicating interaction of ions within the pore of the channel. Consistent with this was the observation of anomalous mole fraction dependence with a mixed solution of thiocyanate and chloride. 3. In addition to the main open level (about 400 pS; excised patch, symmetrical 165 mM-Cl-), three subconductance levels and one supraconductance level were observed. These were concluded to be integral components of the same channel based on coincidence of appearance and identical permeabilities. 4. The channel is voltage dependent, with open probability in excised patches increasing with more positive potentials. The channel was reversibly blocked in a voltage-dependent manner by SITS (4-acetamido-4'-isothiocyanostilbene-2,2'-disulphonic acid), a stilbene derivative, on the cytoplasmic face. 5. Several differences were noted between cell-attached and excised-patch recordings. The multiple conductance level channel was less frequently seen in cell-attached patches but could often be induced to appear by prolonged application of positive voltages. This induced channel in attached patches showed an altered voltage dependence which could be partially mimicked in excised patches by including cyclic AMP and ATP in the solution on the cytoplasmic side of the membrane.
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PMID:Anion channels with multiple conductance levels in a mouse B lymphocyte cell line. 247 28

1. Properties of anion permeation through the membrane of skeletal muscle fibres of the stingray, Taeniura lymma, were studied with intracellular recording and polarization techniques.2. The Cl conductance of the resting membrane in the normal stingray saline at pH 7.7 is 8-10 times greater than the K conductance.3. The Cl conductance decreases with decreasing external pH, with an apparent pK of 5.3, whereas the K conductance is independent of pH between 4 and 9.4. The Q(10) of the Cl conductance is about 2.0, compared with a value of 1.2-1.4 for the K conductance.5. The Cl conductance is proportional to the external Cl concentration when observed after the fibre is equilibrated in the test solution.6. The permeability sequence obtained by potential measurement is SCN > NO(3) > Cl = Br > I > ClO(3) and the permeability ratio is independent of the mole fraction of anions.7. The conductance sequence determined by total replacement of the external Cl with other anion species differs from the permeability sequence and the conductance observed for partial replacement deviates significantly from that expected from the independence principle.8. Possible mechanisms of anion permeation are discussed.
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PMID:Mechanism of anion permeation through the muscle fibre membrane of an elasmobranch fish, Taeniura lymma. 483

1. The permeability of human red cells to (36)Cl(-) and to [(35)S]SO(4) (2-) was studied in the presence of various monovalent anions.2. A maximum decrease of anion permeability was found in a study of the steady-state exchange of (36)Cl in a medium containing 120 mM salicylate. The exchange had a half-time of 3 hr at 0 degrees C, a reduction of normal chloride permeability by a factor of 10(5). The activation energy of chloride exchange decreased from a value of 45 to 22 kcal/mole in the interval between 0 and 10 degrees C. Simultaneous determination of the permeability to potassium and chloride proved that salicylate induced a reversal of the normal selectivity of red cells at 0 degrees C (permeability coefficient P(K) of 3.5 x 10(-9) cm/sec to be compared with a P(Cl) of 2 x 10(-9) cm/sec).3. In contradistinction to the slow movement of (36)Cl, the exchange of [(14)C]salicylate was completed within 4 min, when red cells were suspended at 0 degrees C in the salicylate medium.4. A study of the sulphate permeability at 38 degrees C showed that the rate of steady-state exchange decreased, when chloride was replaced by lyotropic anions other than bromide. The sequence of the permeability decrease was: Cl(-) = Br(-) < I(-) < NO(3) < SCN(-) < salicylate, the same sequence which previously has been shown to increase the permeability to sodium and potassium. The activation energies of sulphate exchange were 32 kcal/mole (chloride medium), and 38 kcal/mole (thiocyanate medium).5. Sufficient data were obtained during the study to demonstrate that when equilibrium has been obtained, there is a good agreement between the values of (36)Cl (cell water)/(36)Cl (extracellular water) and of {[(35)S]SO(4) (cell water)/[(35)S]SO(4) (extracellular water)}((1/2)).6. It is concluded that the anion-induced changes of permeability are due to binding of anions to fixed cationic charges in the red cell membrane.
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PMID:Effect of some monovalent anions on chloride and sulphate permeability of human red cells. 549 37

The effects of external anions on gating of Na channels of frog skeletal muscle were studied under voltage clamp. Anions reversibly shift the voltage dependence of peak sodium permeability and of steady state sodium inactivation towards more negative potentials in the sequence: methanesulfonate less than or equal to Cl- less than or equal to acetate less than Br- less than or equal to NO-3 less than or equal to SO2-4 less than benzenesulfonate less than SCN- less than ClO-4; approximately the lyotropic sequence. Voltage shifts are graded with mole fraction in mixtures and are roughly additive to calcium shifts. The peak PNa is not greatly affected. Except for SO2-4, these anions did not change the Ca++ activity of the solutions as measured with the dye murexide. Shifts of gating can be explained as the electrostatic effect of anion adsorption to the Na channel or to nearby lipid. Such adsorption is expected to follow the lyotropic series. Anions also interfere significantly with the response of a Ca-sensitive membrane electrode following the same sequence of effectiveness as the shifts of gating. The lyotropic anions decrease the Ca++ sensitivity and cause anomalously negative responses of the Ca electrode because these anions are somewhat permeant in the hydrophobic detector membrane.
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PMID:Lyotropic anions. Na channel gating and Ca electrode response. 630 98

Up to a SCN- concentration of about 110 mM, the concentration dependence of SCN- equilibrium exchange in human red cell ghosts can be represented by the superimposition of two flux components. One component shows saturation kinetics, the other does not. The saturable component has an activation enthalpy of 105 kJ/mole, exhibits a trans acceleration by Cl- and can be inhibited by H2DIDS. The nonsaturable component has a much lower activation enthalpy of 33 kJ/mole, is slightly reduced in trans acceleration experiments with Cl- and insensitive to H2DIDS but susceptible to inhibition by phloretin. At SCN- concentrations exceeding 110 mM, the saturable component undergoes irreversible self inhibition while the nonsaturable component remains unaltered. The half saturation concentration of the saturable flux component increases with decreasing pH from 3.0 mM at pH 7.4 to 13.3 mM at pH 6.0. Over this pH range, the maximal flux is only slightly increased from 19 x 10(-12) to 22 x 10(-12) moles x cm-2 x sec-1. The nonsaturable flux component also increases slightly. In accordance with previous observations of Wieth (J. Physiol. (London) 207:563-580, 1970), we find that SCN- increases K+ and Na+ permeability. The induced cation-permeability is considerably smaller than the SCN- exchange and the latter does not show the paradoxical temperature dependence that is known to pertain to the former.
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PMID:The kinetics of anion equilibrium exchange across the red blood cell membrane as measured by means of 35S thiocyanate. 732 31

Single-channel currents through GABA- and glycine-activated chloride channels of post-natal tissue-cultured hippocampal neurons were measured to determine their anion selectivity and their concentration dependence of permeation. Current-voltage relations for both agonists displayed rectification with single-channel conductance increasing at positive potentials. Permeabilities determined from reversal potentials were maximal for anions with a diameter of about 4 A. Larger diameter anions had lower permeabilities, consistent with an approximate pore diameter of 6 A for both agonist-activated channels. The permeability for anions of similar size was greatest for those ions with a more symmetrical charge distribution (e.g. NO3- > Bicarbonate-). The permeability sequence was SCN- > NO3- > I- > Br- > Cl- > Formate- > Acetate- > Bicarbonate- > Gluconate- > F- > Phosphate-, whereas the conductance sequence for anion efflux was Cl- > Br- > NO3- > I- > SCN- > Formate- > Acetate- > Bicarbonate- > Gluconate- > F- > Phosphate-. These results suggest that the ions interact with sites within the channel, with hydration forces contributing an important component to the barrier for ion entry into the channel. The spherically symmetrical halides displayed an exponential relation between relative permeability and hydration energy. Concentration dependence of conductance for Cl- channels in symmetrical Cl- solutions with agonist in the pipette showed an increase at positive potentials and a decrease at negative potentials. GABA- and glycine-activated channels also exhibited anomalous mole-fraction effects in a mixture of Cl- and SCN-. These results suggest that both agonist-activated channels act as multi-ion pathways and have similar permeation characteristics.
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PMID:Anion permeation in GABA- and glycine-gated channels of mammalian cultured hippocampal neurons. 769 Apr 84


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