Activation of potassium conductance in squid axons with membrane depolarization is delayed by conditioning hyperpolarization of the membrane potential. The delayed kinetics superpose with the control kinetics almost, but not quite, exactly following time translation, as demonstrated previously in perfused axons by Clay and Shlesinger (1982). Similar results were obtained in this study from nonperfused axons. The lack of complete superposition argues against the Hodgkin and Huxley (1952) model of potassium conductance. The addition of a single kinetic state to their model, accessible only by membrane hyperpolarization, is sufficient to describe this effect (Young and Moore, 1981)
We describe a kinetic reaction sequence for the sodium conductance system in the squid axon. It clos...
Two illustrative molecular models, designed to explain the Cole-Moore K+ hyperpolarization delay, ar...
The solutions, n(t), of the differential equation dn/dt = α (1 - n) n (4 - 6n + 4n2 - n3) - βn2 (4 -...
Activation of potassium conductance in squid axons with membrane depolarization is delayed by condit...
Potassium ion current in squid axons is usually modified by the effects of ion accumulation in the p...
The original experiments of Cole and Moore (1960. Biophys. J. 1:161–202.), using conditioning and te...
The original experiments of Cole and Moore (1960. Biophys. J. 1:161–202.), using conditioning and te...
Potassium ion current in squid axons is usually modified by the effects of ion accumulation in the p...
A slow potassium inactivation i.e. decrease of conductance when the inside of the membrane is made m...
The kinetics of the voltage-sensitive potassium channel in crayfish axon have been examined. The con...
A slow potassium inactivation i.e. decrease of conductance when the inside of the membrane is made m...
The kinetics of the voltage-sensitive potassium channel in crayfish axon have been examined. The con...
The kinetics of potassium conductance changes were determined in the voltage clamped frog node (Rana...
Hyperpolarizing conditioning pulses delay the onset of potassium channel current in voltage-clamped ...
We describe a kinetic reaction sequence for the sodium conductance system in the squid axon. It clos...
We describe a kinetic reaction sequence for the sodium conductance system in the squid axon. It clos...
Two illustrative molecular models, designed to explain the Cole-Moore K+ hyperpolarization delay, ar...
The solutions, n(t), of the differential equation dn/dt = α (1 - n) n (4 - 6n + 4n2 - n3) - βn2 (4 -...
Activation of potassium conductance in squid axons with membrane depolarization is delayed by condit...
Potassium ion current in squid axons is usually modified by the effects of ion accumulation in the p...
The original experiments of Cole and Moore (1960. Biophys. J. 1:161–202.), using conditioning and te...
The original experiments of Cole and Moore (1960. Biophys. J. 1:161–202.), using conditioning and te...
Potassium ion current in squid axons is usually modified by the effects of ion accumulation in the p...
A slow potassium inactivation i.e. decrease of conductance when the inside of the membrane is made m...
The kinetics of the voltage-sensitive potassium channel in crayfish axon have been examined. The con...
A slow potassium inactivation i.e. decrease of conductance when the inside of the membrane is made m...
The kinetics of the voltage-sensitive potassium channel in crayfish axon have been examined. The con...
The kinetics of potassium conductance changes were determined in the voltage clamped frog node (Rana...
Hyperpolarizing conditioning pulses delay the onset of potassium channel current in voltage-clamped ...
We describe a kinetic reaction sequence for the sodium conductance system in the squid axon. It clos...
We describe a kinetic reaction sequence for the sodium conductance system in the squid axon. It clos...
Two illustrative molecular models, designed to explain the Cole-Moore K+ hyperpolarization delay, ar...
The solutions, n(t), of the differential equation dn/dt = α (1 - n) n (4 - 6n + 4n2 - n3) - βn2 (4 -...