A, Representative examples of Ca currents elicited by repetitive 3 Hz depolarizing voltage steps to 0 mV from a holding potential of −40 mV from a CA1.

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Fig. 1 (A) Average current voltage relations of peak INa in Con (n=10), nAF (n=7) and cAF (n=9) cells using protocol shown on left. (B) Average.
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A, Representative examples of Ca currents elicited by repetitive 3 Hz depolarizing voltage steps to 0 mV from a holding potential of −40 mV from a CA1 neuron of a young-adult animal (top) and an aged animal (bottom). A, Representative examples of Ca currents elicited by repetitive 3 Hz depolarizing voltage steps to 0 mV from a holding potential of −40 mV from a CA1 neuron of a young-adult animal (top) and an aged animal (bottom). Voltage steps (actual) shown in the lowest trace ofA are from the aged cell shown above. Currents were obtained for five 200 msec pulses given at 3 Hz. Holding potentials of −40 mV reduced the rapidly inactivating component and allowed more accurate measures of the slowly inactivating Ca current.B, Mean ± SEM of peak (a) and late (b) current measured in the protocol shown inA. The charge carrier was 2 mm Ca. Both peak and late Ca currents were significantly larger in neurons from aged (n = 22) than from young adult (n = 25) animals, but a significant interaction was found between age and repetitive pulses only for peak current (a). C, Mean ± SEM of peak (a) and late (b) current in neurons (n = 12 adult and 11 aged neurons) with Ba (2 mm) substituted for Ca as the charge carrier. The aging difference still is apparent, but the overall rate of inactivation is slowed. However, a significant interaction between age and repetitive pulses was present for both peak and late currents, possibly reflecting greater inactivation in the aged group. Lee W. Campbell et al. J. Neurosci. 1996;16:6286-6295 ©1996 by Society for Neuroscience