Аннотация
1. Voltage clamp recordings of the calcium current (ICa) in single
myocytes which were enzymatically isolated from bull-frog atrium
show that a genuine reversal of the current flowing through Ca2+
channels can be recorded (ef. Reuter & Scholz, 1977; Lee & Tsien,
1982, 1984; Campbell, Giles & Shibata, 1988c). In normal 2.5 mM Ca2+0
Ringer solution this apparent reversal potential (Erev) is near +50
mV, a value well below the predicted thermodynamic Ca2+ equilibrium
potential (ECa). 2. None the less, Erev shifts with variations in
extracellular divalent ion concentrations (Ca2+, Sr2+ and Ba2+) according
to the predictions of a Nernstian divalent cation electrode, i.e.
approximately 29 mV per 10-fold change in the external concentration
of divalent ion. 3. The existing theoretical analysis of this Erev
has been extended in order to clarify its interpretation with regard
to the selectivity characteristics of ICa. 4. The apparent reversal
potential is analysed using a form of the constant field equation
which has been modified to include (i) simultaneous monovalent and
divalent cation movements and (ii) the presence of a surface potential
(V'). This equation can be solved to yield an explicit expression
for Erev. The effects of V' on apparent permeability ratios for the
Ca2+ channel Erev are demonstrated. 5. In combination, our experimental
results and calculations suggest that: (i) previous estimates of
V' which were used to describe permeability (P) ratios of Ca2+ channels
in various cardiac preparations may be in error, (ii) in normal Ca2+o
the PNa/PCa ratio is very small, and (iii) PCa/PK must be greater
than 1000. An analysis of the relative selectivity of the channel
for divalent cations compared to K+ shows that PCa greater than PSr
greater than PBa, assuming that PK remains the same after the divalent
substitutions. 6. The Ca2+ channel in bull-frog atrial cells is thus
much more selective for Ca2+ ions than had previously been estimated;
in particular, inward flow of monovalent cations (e.g. Na+) through
these channels does not contribute significantly to the observed
ICa. The physiological implications of this high selectivity for
Ca2+ ions are discussed.
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