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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Pflügers Archiv 407 (1986), S. S112 
    ISSN: 1432-2013
    Schlagwort(e): Ciliary epithelium ; Shark ; Intracellular membrane potential ; Intracellular chloride activity ; Ouabain ; Furosemide
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract We have found that membrane potential in the isolated ciliary epithelium of the shark,Squalus acanthias, is −53 mV. High extracellular potassium or ouabain (10−5 mol·l−1) decrease the potential, and furosemide (10−4 mol·l−1) hyperpolarizes it. There is no difference in membrane potential between the cells of the non-pigmented and pigmented layers. Intracellular chloride activity (64 mmol·l−1) was significantly higher than could be predicted from the equilibrium distribution (26 mmol·l−1) across the cell membranes. When furosemide was applied to the aqueous side of the epithelium, intracellular chloride activity decreased to 35 mmol·l−1 and approached electrochemical equilibrium. The data indicate that the ciliary epithelium possesses an active, furosemide-sensitive chloride transport mechanism which could be a Na−Cl or a 1 Na-1 K-2 Cl symport.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1432-2013
    Schlagwort(e): Ciliary epithelium ; Tissue culture ; Na+/H+ exchange ; Amiloride
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Uptake studies with22Na were performed in cultured bovine pigmented ciliary epithelial cells, in order to characterize mechanisms of Na+ transport. A large part of Na+ uptake was sensitive to amiloride, quinidine and harmaline. Na+ uptake was stimulated by intracellular acidification (using the NH 4 + prepulse technique), and was inhibited with increasing extracellular proton concentration. Decreasing extracellular pH from 7.5 to 7.0 increased the apparentK M for Na+ from 38 to 86 mM without considerable changes inV max. In the presence of 5 mM Na+ half maximal inhibition of amiloride sensitive Na+ uptake by extracellular protons was observed at a hydrogen concentration of 50 nM. In the presence of 50 mM Na+ the proton concentration necessary for 50% inhibition was 139 nM. Thus, the mode of inhibition of extracellular H+ seemed to be competitive with aK i of 20–40 nM. 10 μM amiloride increased the apparentK M for Na+ from 33 mM to 107 mM, whileV max remained nearly unchanged. IC50 for amiloride was 6 μM at 5 mM Na+ and 36 μM in the presence of 150 mM Na+. Thus, amiloride behaves as a competitive inhibitor with aK i of about 5 μM. The affinities of Na+ to the transport site (K M≈16 mM), to the inhibitory site for protons (K M≈21 mM), and to the inhibitory site for amiloride (K M≈26 mM) were in the same order of magnitude. In summary, we have presented evidence for the presence of a Na+/H+ exchanger in cultured bovine pigmented ciliary epithelial cells. The kinetic data suggest the presence of only one common extracellular binding site for Na+, H+ and amiloride.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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