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  • 1985-1989  (2)
  • 1950-1954
  • 1935-1939
  • Na pump flux  (1)
  • sodium transport  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 92 (1986), S. 37-46 
    ISSN: 1432-1424
    Keywords: frog skin ; cell Na activity ; membrane potential ; Na pump flux ; Na microelectrodes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Cell Na activity,a Na c , was measured in the short-circuited frog skin by simulaneous cell punctures from the apical surface with open-tip and Na-selective microelectrodes. Skins were bathed on the serosal surface with NaCl Ringer and, to reduce paracellular conductance, with NaNO3 Ringer on the apical surface. Under control conditionsa Na c averaged 8±2mm (n=9,sd). Apical addition of amiloride (20 μm) or Na replacement reduceda Na c to 3mm in 6–15 min. Sequential decreases in apical [Na] induced parallel reductions ina Na c and cell current,I c . On restoring Na after several minutes of exposure to apical Na-free solutionI c rose rapidly $$(\tilde〈 30\sec )$$ to a stable value whilea Na c increased exponentially, with a time constant of 1.8±0.7 min (n=8). Analysis of the time course ofa Na c indicates that the pump Na flux is linearly related toa Na c in the range 2–12mm. These results indicate thata Na c plays an important role in relating apical Na entry to basolateral active Na flux.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 106 (1988), S. 13-28 
    ISSN: 1432-1424
    Keywords: cell potential ; amiloride ; sodium transport ; reversal potential
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Knowledge of the voltage dependencies of apical and basolateral conductances is important in determining the factors that regulate transcellular transport. To gain this knowledge it is necessary to distinguish between cellular and paracellular currents and conductances. This is generally done by sequentially measuring transepithelial current/voltage (I t /V t ) and conductance/voltage (g t /V t ) relationships before and after the abolition of cellular sodium transport with amiloride. Often, however, there are variable time-dependent and voltage-dependent responses to voltage perturbation both in the absence and presence of amiloride, pointing to effects on the paracellular pathway. We have here investigated these phenomena systematically and found that the difficulties were significantly lessened by the use of an intermittent technique, measuringI t andg t before and after brief (〈10 sec) exposure to amiloride at each setting ofV t .I/V relationships were characterized by these means in frog skins (Rana pipiens, Northern variety, andRana temporaria). Cellular current,I c , decreased with hyperpolarization (larger serosa positive clamps) ofV t . DerivedI c /V t relationships betweenV t =0 and 175 mV (serosa positive) were slightly concave upwards. Because values of cell conductance,g c , remained finite, it was possible to demonstrate reversal ofI c . Values of the reversal potentialV' averaged 156±14 (sd,n=18) mV. Simultaneous microelectrode measurements permitted also the calculation of apical and basolateral conductances,g a andg b . The apical conductance decreased monotonically with increasing positivity ofV t (andV a ). In contrast, in the range in which the basolateral conductance could be evaluated adequately (V t 〈125 mV),g b increased with more positive values ofV t (andV b ). That is, there was an inverse relation betweeng b and cellular current at the quasi-steady state, 10–30 sec after the transepithelial voltage step.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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