Abstract
Conduction in inward rectifier, K+-channels in Aplysia neuron and Ba++ blockade of these channels were studied by rapid measurement of the membrane complex admittance in the frequency range 0.05 to 200 Hz during voltage clamps to membrane potentials in the range -90 to -40 mV. Complex ionic conductances of K+ and Cl- rectifiers were extracted from complex admittances of other membrane conduction processes and capacitance by vector subtraction of the membrane complex admittance during suppressed inward K+ current (near zero-mean current and in zero [K+]0) from complex admittances determined at other [K+]0 and membrane potentials. The contribution of the K+ rectifier to the admittance is distinguishable in the frequency domain above 1 Hz from the contribution of the Cl- rectifier, which is only apparent at frequencies less than 0.1 Hz. The voltage dependence (-90 to -40 mV) of the chord conductance (0.2 to 0.05 microS) and the relaxation time (4-8 ms) of K+ rectifier channels at [K+]0 = 40 mM were determined by curve fits of admittance data by a membrane admittance model based on the linearized Hodgkin-Huxley equations. The conductance of inward rectifier, K+ channels at a membrane potential of -80 mV had a square-root dependence on external K+ concentration, and the relaxation time increased from 2 to 7.5 ms for [K+]0 = 20 and 100 mM, respectively. The complex conductance of the inward K+ rectifier, affected by Ba++, was obtained by complex vector subtraction of the membrane admittance during blockage of inward rectifier, K+ channels (at -35 mV and [Ba++]0 = 5 mM) from admittances determined at -80 mV and at other Ba++ concentrations. The relaxation time of the blockade process decreased with increases in Ba++ concentration. An open-closed channel state model produces the inductive-like kinetic behavior in the complex conductance of inward rectifier, K+ channels and the addition of a blocked channel state accounts for the capacitive-like kinetic behavior of the Ba++ blockade process.
Full text
PDF










Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Adrian R. H., Chandler W. K., Hodgkin A. L. Slow changes in potassium permeability in skeletal muscle. J Physiol. 1970 Jul;208(3):645–668. doi: 10.1113/jphysiol.1970.sp009140. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Adrian R. H., Freygang W. H. The potassium and chloride conductance of frog muscle membrane. J Physiol. 1962 Aug;163(1):61–103. doi: 10.1113/jphysiol.1962.sp006959. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brodwick M. S., Junge D. Post-stimulus hyperpolarization and slow potassium conductance increase in Aplysia giant neurone. J Physiol. 1972 Jun;223(2):549–570. doi: 10.1113/jphysiol.1972.sp009862. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CHANDLER W. K., FITZHUGH R., COLE K. S. Theoretical stability properties of a space-clamped axon. Biophys J. 1962 Mar;2:105–127. doi: 10.1016/s0006-3495(62)86844-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chesnoy-Marchais D. Characterization of a chloride conductance activated by hyperpolarization in Aplysia neurones. J Physiol. 1983 Sep;342:277–308. doi: 10.1113/jphysiol.1983.sp014851. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cuthbert A. W. Importance of guanidinium groups of blocking sodium channels in epithelia. Mol Pharmacol. 1976 Nov;12(6):945–957. [PubMed] [Google Scholar]
- Eckert R., Lux H. D. A voltage-sensitive persistent calcium conductance in neuronal somata of Helix. J Physiol. 1976 Jan;254(1):129–151. doi: 10.1113/jphysiol.1976.sp011225. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fishman H. M., Leuchtag H. R., Moore L. E. Fluctuation and linear analysis of Na-current kinetics in squid axon. Biophys J. 1983 Sep;43(3):293–307. doi: 10.1016/S0006-3495(83)84353-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gallin E. K. Voltage clamp studies in macrophages from mouse spleen cultures. Science. 1981 Oct 23;214(4519):458–460. doi: 10.1126/science.7291986. [DOI] [PubMed] [Google Scholar]
- Geduldig D., Gruener R. Voltage clamp of the Aplysia giant neurone: early sodium and calcium currents. J Physiol. 1970 Nov;211(1):217–244. doi: 10.1113/jphysiol.1970.sp009276. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gunning R. Steady state current noise from the intrinsic gating of inward rectifier channels. Biophys J. 1984 May;45(5):1031–1035. doi: 10.1016/S0006-3495(84)84249-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HAGIWARA S., KUSANO K., SAITO N. Membrane changes of Onchidium nerve cell in potassium-rich media. J Physiol. 1961 Mar;155:470–489. doi: 10.1113/jphysiol.1961.sp006640. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HUTTER O. F., NOBLE D. Rectifying properties of heart muscle. Nature. 1960 Nov 5;188:495–495. doi: 10.1038/188495a0. [DOI] [PubMed] [Google Scholar]
- Hagiwara S., Takahashi K. The anomalous rectification and cation selectivity of the membrane of a starfish egg cell. J Membr Biol. 1974;18(1):61–80. doi: 10.1007/BF01870103. [DOI] [PubMed] [Google Scholar]
- Hestrin S. The interaction of potassium with the activation of anomalous rectification in frog muscle membrane. J Physiol. 1981 Aug;317:497–508. doi: 10.1113/jphysiol.1981.sp013839. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kandel E. R., Tauc L. Anomalous rectification in the metacerebral giant cells and its consequences for synaptic transmission. J Physiol. 1966 Mar;183(2):287–304. doi: 10.1113/jphysiol.1966.sp007867. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Leech C. A., Stanfield P. R. Inward rectification in frog skeletal muscle fibres and its dependence on membrane potential and external potassium. J Physiol. 1981;319:295–309. doi: 10.1113/jphysiol.1981.sp013909. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marmor M. F. The effects of temperature and ions on the current-voltage relation and electrical characteristics of a molluscan neurone. J Physiol. 1971 Nov;218(3):573–598. doi: 10.1113/jphysiol.1971.sp009634. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Matsuda H., Saigusa A., Irisawa H. Ohmic conductance through the inwardly rectifying K channel and blocking by internal Mg2+. Nature. 1987 Jan 8;325(7000):156–159. doi: 10.1038/325156a0. [DOI] [PubMed] [Google Scholar]
- Meech R. W., Standen N. B. Potassium activation in Helix aspersa neurones under voltage clamp: a component mediated by calcium influx. J Physiol. 1975 Jul;249(2):211–239. doi: 10.1113/jphysiol.1975.sp011012. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miyamoto S., Fishman H. M. Na conductance kinetics in the low-frequency impedance of isolated snail neurons. IEEE Trans Biomed Eng. 1986 Jul;33(7):644–653. doi: 10.1109/TBME.1986.325754. [DOI] [PubMed] [Google Scholar]
- NAKAJIMA S., IWASAKI S., OBATA K. Delayed rectification and anomalous rectification in frog's skeletal muscle membrane. J Gen Physiol. 1962 Sep;46:97–115. doi: 10.1085/jgp.46.1.97. [DOI] [PMC free article] [PubMed] [Google Scholar]
- REUBEN J. P., GAINER H. Membrance conductance during depolarizing postsynaptic potentials of crayfish muscle fibres. Nature. 1962 Jan 13;193:142–143. doi: 10.1038/193142a0. [DOI] [PubMed] [Google Scholar]
- TAUC L., KANDEL E. R. AN ANOMALOUS FORM OF RECTIFICATION IN A MOLLUSCAN CENTRAL NEURONE. Nature. 1964 Jun 27;202:1339–1341. doi: 10.1038/2021339a0. [DOI] [PubMed] [Google Scholar]
- Vandenberg C. A. Inward rectification of a potassium channel in cardiac ventricular cells depends on internal magnesium ions. Proc Natl Acad Sci U S A. 1987 Apr;84(8):2560–2564. doi: 10.1073/pnas.84.8.2560. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Warncke J., Lindemann B. Voltage dependence of Na channel blockage by amiloride: relaxation effects in admittance spectra. J Membr Biol. 1985;86(3):255–265. doi: 10.1007/BF01870605. [DOI] [PubMed] [Google Scholar]
- Werblin F. S. Time- and voltage-dependent ionic components of the rod response. J Physiol. 1979 Sep;294:613–626. doi: 10.1113/jphysiol.1979.sp012949. [DOI] [PMC free article] [PubMed] [Google Scholar]