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Calcium Current in the Unfertilized Egg of the Hamster

Calcium Current in the Unfertilized Egg of the Hamster

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The presence of a calcium current (i<sub>Ca<sup>2+</sup></sub>) passed via a specific channel was examined in the unfertilized hamster egg using the whole-cell voltage clamp technique. Pure inward current was isolated using a Ca<sup>2+</sup>-rich pipette solution containing 10 mM TEA. This current was independent of external Na<sup>+</sup> and was highly sensitive to the Ca<sup>2+</sup> concentration in the bathing solution, indicating that the inward current is carried by Ca<sup>2+</sup>. The maximal amplitude was -4.12±0.58nA (n=12) with 10mM Ca<sup>2+</sup> at -3OmV from a holding potential of -8OmV. This current reached its maximum within 20ms beyond -3OmV and decayed rapidly with an inactivation time constant τ of 15ms. Activation and inactivation of this i<sub>Ca<sup>2+</sup></sub> was steeply dependent on the membrane potential. The i<sub>Ca<sup>2+</sup></sub> began to activate at the lower voltage of -55 mV and reached its peak at -35 mV, being completely inactivated at potentials more positive than -40 mV. These result suggest that i<sub>Ca<sup>2+</sup></sub> in hamster eggs passes through channels with electrical properties similar to low voltage-activated T-type channels. Other results from the present study support this suggestion; First, the inhibitory effect of Ni<sup>2+</sup> (IC<sub>50</sub>=13.7 μM) was more potent than Cd<sup>2+</sup> (IC<sub>50</sub>=123 μM). Second, Ba<sup>2+</sup> conductance was equal to or below that of Ca<sup>2+</sup>. Third, i<sub>Ca<sup>2+</sup></sub> in hamster eggs was relatively insensitive to nifedipine (IC<sub>50</sub>=96.6 μM), known to be a specific t-type blocker. The physiological role of i<sub>Ca<sup>2+</sup></sub> in the unfertilized hamster eggs remains unclear. Analysis from steady-state inactivation activation curves reveals that only a small amount of this current will pass in the voltage range (-70 ~ -30 mV) which partially overlaps with the resting membrane potential. This current has the property that it can be easily activated by a weak depolarization, thus it may trigger a certain kind of a intracellular event following fertilization which may cause oscillations in the membrane potential.

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