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Biophys J, April 1999, p. 1959-1971, Vol. 76, No. 4
*Department of Physiology,
We have investigated actions of various divalent
cations (Ba2+, Sr2+, Mn2+,
Co2+, Ni2+, Zn2+) on human
ether-a-go-go related gene (HERG) channels expressed in Xenopus
laevis oocytes using the voltage clamp technique. All divalent
cations inhibited HERG current dose-dependently in a voltage-dependent
manner. The concentration for half-maximum inhibition (Ki) decreased at more negative potentials,
indicating block is facilitated by hyperpolarization.
Ki at 0 mV for Zn2+,
Ni2+, Co2+, Ba2+, Mn2+,
and Sr2+ was 0.19, 0.36, 0.50, 0.58, 2.36, and 6.47 mM,
respectively. The effects were manifested in four ways: 1) right shift
of voltage dependence of activation, 2) decrease of maximum
conductance, 3) acceleration of current decay, and 4) slowing of
activation. However, each parameter was not affected by each cation to
the same extent. The potency for the shift of voltage dependence of activation was in the order Zn2+ > Ni2+
Biophys J, April 1999, p. 1959-1971, Vol. 76, No. 4
Co2+ > Ba2+ > Mn2+ > Sr2+, whereas the potency for the decrease of maximum
conductance was Zn2+ > Ba2+ > Sr2+ > Co2+ > Mn2+. The kinetics
of activation and deactivation were also affected, but the two
parameters are not affected to the same extent. Slowing of activation
by Ba2+ was most distinct, causing a marked initial delay
of current onset. From these results we concluded that HERG channels
are nonselectively blocked by most divalent cations from the external side, and several different mechanism are involved in their actions. There exist at least two distinct binding sites for their action: one
for the voltage-dependent effect and the other for reducing maximum conductance.
© 1999 by the Biophysical Society 0006-3495/99/04/1959/13 $2.00
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