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  • Flounder, (Pseudopleuronectes americanus)  (1)
  • epithelial transport  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 93 (1986), S. 259-269 
    ISSN: 1432-1424
    Keywords: ionic channels ; epithelial transport ; lens physiology ; patch clamp ; pressure-activated channels ; cataracts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Patch-clamp recording from the apical surface of the epithelium of frog lens reveals a cation-selective channel after pressure (about ±30 mm Hg) is applied to the pipette. The open state of this channel has a conductance of some 50 pS near the resting potential (−56.1±2.3 mV) when 107mm NaCl and 10 HEPES (pH 7.3) is outside the channel. The probability of the channel being open depends strongly on pressure but the current-voltage relation of the open state does not. With minimal Ca2+ (55±2 μm) outside the channel, the current-voltage relation is nonlinear even in symmetrical salt solutions, allowing more current to flow into the cell than out. The channel, in minimal Ca2+ solution, is selective among the monovalent cations in the following sequence K+〉Rb+〉Cs+〉Na+〉Li+. The conductance depends monotonically on the mole fraction of K+ when the other ion present is Li+ or Na+. The single-channel current is a saturating function of [K+] when K+ is the permeant ion, for [K+]≤214mm. When [Ca2+]=2mm, the currentvoltage relation is linearized and the channel cannot distinguish Na+ and K+.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 163 (1993), S. 581-586 
    ISSN: 1432-136X
    Keywords: Ion transport ; Membrane transport ; Intestine ; K secretion ; Flounder, (Pseudopleuronectes americanus)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Enterocytes from the winter flounder (Pseudopleuronectes americanus) were isolated by collagenase digestion and maintained in flounder Ringer's solution. Whole cell currents were studied using the amphotericin-perforated whole-cell patch clamp technique. The mean resting membrane potential and capacitance values or dissociated cells were-45±7 mV and 5±0.4 pF, respectively. Enterocytes held at-20 mV and treated with 1 μmol·l-1 ionomycin exhibited outward currents when cells were stepped through a series of voltages from-60 to +110 mV. The reversal potential of this current in flounder Ringer's solution was-55 mV and the voltage at which half-maximal activation occurred was +20 mV. Voltage-dependent inhibition of outward current was observed at +60 mV and above. When cells were bathed in symmetric K Ringer's solution the reversal potential shifted to zero mV and no inhibition of current was observed at voltages between-60 and 140 mV. When the holding potential of the cell was changed from-20 to-80 mV and stepped from-60 to +110 mV, a second [previously characterized, O'Grady et al. (1991)] K current with delayed-rectifier properties was identified. This observation demonstrated that the delayed rectifier K channel and the Ca2+-activated K channel described in this study exist in the same cell. Extracellular addition of 2 mmol·l-1 Ba2+ to cells bathed in symmetric K Ringer's solution resulted in nearly complete inhibition of outward current. Charybdotoxin produced only minor effects on this current. Addition of 8-Br cGMP to the bathing solution also inhibited outward current and this effect could be partially reversed following washout of 8-Br cGMP from the bathing solution. The results of this study indicated that a Ca2+-activated K conductance in winter flounder enterocytes is potentially inhibited by agents that increase intracellular cGMP. A similar effect of cGMP on a delayed rectifier K channel in flounder enterocytes was previously demonstrated.
    Type of Medium: Electronic Resource
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