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Department of Biophysics, School of Biological Sciences, University of East Anglia, Norwich NR4 7TJ
1. The steady-state and kinetic characteristics of the processes of activation and inactivation of the Na+ permeability, PNa, were measured in cut skeletal muscle fibres from Rana temporaria under voltage-clamp conditions.
2. The specific resistance, rss, in series with the surface sarcolemma, was estimated as 6
cm2 by measuring the initial value of the membrane potential transient in response to current pulses under current-clamp conditions. To reduce the error in the potential across the sarcolemma introduced by rss, Na+ currents were recorded using positive feed-back compensation, in the presence of tetrodotoxin (2·4-5 nM).
3. PNa(t) was fitted with m3h kinetics assuming a voltage-dependent delay,
t, to the start of the activation process.
4. The PNaVp curve exhibited saturation at potentials more positive than 30 mV. m
, calculated as (PNa,
/
Na)
as a function of Vp, was a sigmoid curve with a mid point at -35 mV. The slope, dm
/dVp, at this point was 0·032 mV-1.
5. Using a double-pulse protocol a non-exponential time course for the development of fast inactivation at small depolarizations was observed.
6. The time constant for activation,
m, as a function of Vp, and
h as a function of Vp, could be fitted with an approximately bell-shaped function, maximum of 430 µs at -43 mV and 925 µs at -78 mV respectively, at 15 °C.
7. The mid-point potential of the h
Vl curve occurred at -58 mV, and h
approached 1 for V1 values more negative than -103 mV.
8. Using a double-pulse procedure the development of a slow inactivation of the Na+ current was demonstrated. Its time course could be described in terms of a single exponential function, time constant equal to 0·58 s. The recovery from slow inactivation could be described by a similar exponential for recovery times smaller than 1 s.
Present address: Laboratory of Neurosciences, Gerontology Research Center, Baltimore City Hospitals, Baltimore, MD 21224, U.S.A.
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