The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
Potassium activation in Helix aspersa neurones under voltage clamp: a component mediated by calcium influx.
Open accessAbstract
1. Helix aspersa neurones under voltage clamp generate prolonged outward currents (potassium currents) in response to depolarizing command pulses. 2. The potassium currents recorded from cell A were reversibly reduced 25–50% by 10 mM cobalt ions in the bathing medium; 1 mM lanthanum, 10(−6) g/ml. D‐600 and 10(−6) g/ml. iproveratril had similar effects but were only partially reversible. 3. The relationship between the potassium currents and the membrane potential had an “n” shape in normal saline. In calcium‐free saline (containing 25 mM magnesium) the potassium currents were reduced and the “n” shape was abolished. The effect of calcium‐free saline was readily reversible. 4. The voltage‐dependence of the calcium‐sensitive potassium currents was similar to that of the “late” calcium channel in squid axons (Baker, Hodgkin & Ridgway, 1971). 5. When cell A was depolarents were made up of two exponentially declining components. The slower of the two components was reduced in calcium‐free saline. 6. When cell A was depolarized by 150 mV for 10 msec and then repolarized the “tail” currents were made up of a single rapidly declining component. The reversal potential of this component changed by 58 mV for a tenfold change in the external potassium concentration as predicted by the Nernst equation. 7. The reversal potential of “tail” currents having both components was less sensitive to changes in the external potassium concentration. 8. Tetraethylammonium (TEA) ions blocked both calcium dependent and voltage sensitive potassium currents. Each receptor was found to bind a single molecule of TEA. The dissociaton constant was about 10 mM in each case. 9. The intracellular concentration of ionized calcium was estimated from the potential at which there was no apparent calcium influx (the null point). It was between 3 x 10(−8) M and 8 x 10(−8) M with 10(−2) M calcium in the bathing medium. 10. The null point changed 30 mV for a tenfold change in the external calcium concentration as predicted by the Nernst equation. 11. It is concluded that depolarization of Helix neurones activates two typesof potassium channel. One channel is voltage dependent and highly selective for potassium. Activation of the other channel is dependent on the influx (or injection, see Meech, 1972, 1974a) of calcium. This calcium mediated potassium activation system saturates at high external calcium concentrations and is inhibited by external magnesium ions.
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Citations
Cites
Measurement of current‐voltage relations in the membrane of the giant axon of Loligo
Hodgkin, A. L., Huxley, A. F., & Katz, B. (1952) · The Journal of Physiology · doi:10.1113/jphysiol.1952.sp004716 · Cited by 1,733
The dual effect of membrane potential on sodium conductance in the giant axon of Loligo
Hodgkin, A. L., & Huxley, A. F. (1952) · The Journal of Physiology · doi:10.1113/jphysiol.1952.sp004719 · Cited by 1,600
The components of membrane conductance in the giant axon of Loligo
Hodgkin, A. L., & Huxley, A. F. (1952) · The Journal of Physiology · doi:10.1113/jphysiol.1952.sp004718 · Cited by 1,401
A study of synaptic transmission in the absence of nerve impulses
Katz, B., & Miledi, R. (1967) · The Journal of Physiology · doi:10.1113/jphysiol.1967.sp008307 · Cited by 899
Depolarization and calcium entry in squid giant axons
Baker, P. F., Hodgkin, A. L., & Ridgway, E. B. (1971) · The Journal of Physiology · doi:10.1113/jphysiol.1971.sp009641 · Cited by 728
Movements of labelled calcium in squid giant axons
Hodgkin, A. L., & Keynes, R. D. (1957) · The Journal of Physiology · doi:10.1113/jphysiol.1957.sp005850 · Cited by 663
Tetrodotoxin‐resistant electric activity in presynaptic terminals
Katz, B., & Miledi, R. (1969) · The Journal of Physiology · doi:10.1113/jphysiol.1969.sp008875 · Cited by 615
The electrical properties of crustacean muscle fibres
Fatt, P., & Katz, B. (1953) · The Journal of Physiology · doi:10.1113/jphysiol.1953.sp004884 · Cited by 579
The Selective Inhibition of Delayed Potassium Currents in Nerve by Tetraethylammonium Ion
Hille, B. (1967) · The Journal of General Physiology · doi:10.1085/jgp.50.5.1287 · Cited by 490
The kinetics and rectifier properties of the slow potassium current in cardiac Purkinje fibres
Noble, D., & Tsien, R. W. (1968) · The Journal of Physiology · doi:10.1113/jphysiol.1968.sp008454 · Cited by 490
Cited by
Llinás, R. R. (1988) · Science · doi:10.1126/science.3059497 · Cited by 2,285
Eckert, R., & Chad, J. E. (1984) · Progress in Biophysics and Molecular Biology · doi:10.1016/0079-6107(84)90009-9 · Cited by 608
Intracellular Ca2+ activates a fast voltage-sensitive K+ current in vertebrate sympathetic neurones
Adams, P. R., Constanti, A., Brown, D. A., & Clark, R. B. (1982) · Nature · doi:10.1038/296746a0 · Cited by 417
Single channel recordings of Ca2+-activated K+ currents in rat muscle cell culture
Pallotta, B. S., Magleby, K. L., & Barrett, J. N. (1981) · Nature · doi:10.1038/293471a0 · Cited by 414
Somatostatin Signaling in Neuronal Cilia Is Criticalfor Object Recognition Memory
Einstein, E. B., Patterson, C. A., Hon, B. J., Regan, K. A., Reddi, J., Melnikoff, D. E., Mateer, M. J., Schulz, S., Johnson, B. N., & Tallent, M. K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5295-09.2010 · Cited by 129
Metadata
- Authors
- Meech, R. W., & Standen, N. B.
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 1975-07
- Volume
- 249
- Issue
- 2
- Pages
- 211-259
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- OpenAlex
- W2081299190
- Cited by
- 624
- References
- 17
- FWCI
- 17.86
- Type
- journal article
- Language
- en
- Open access
- green
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