Abstract
A large patch electrode was used to measure local currents from the cell bodies of Aplysia neurons that were voltage-clamped by a two-microelectrode method. Patch currents recorded at the soma cap, antipodal to the origin of the axon, and whole-cell currents were recorded simultaneously and normalized to membrane capacitance. The patch electrode could be reused and moved to different locations which allowed currents from adjacent patches on a single cell to be compared. The results show that the current density at the soma cap is smaller than the average current density in the cell body for three components of membrane current: the inward Na current (INa), the delayed outward current (Iout), and the transient outward current (IA). Of these three classes of ionic currents, IA is found to reach the highest relative density at the soma cap. Current density varies between adjacent patches on the same cell, suggesting that ion channels occur in clusters. The kinetics of Iout, and on rare occasions IA, were also found to vary between patches. Possible sources of error inherent to this combination of voltage clamp techniques were identified and the maximum amplitudes of the errors estimated. Procedures necessary to reduce errors to acceptable levels are described in an appendix.
Full text
PDF









Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Adams D. J., Smith S. J., Thompson S. H. Ionic currents in molluscan soma. Annu Rev Neurosci. 1980;3:141–167. doi: 10.1146/annurev.ne.03.030180.001041. [DOI] [PubMed] [Google Scholar]
- Aldrich R. W., Jr, Getting P. A., Thompson S. H. Inactivation of delayed outward current in molluscan neurone somata. J Physiol. 1979 Jun;291:507–530. doi: 10.1113/jphysiol.1979.sp012828. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Almers W., Roberts W. M., Ruff R. L. Voltage clamp of rat and human skeletal muscle: measurements with an improved loose-patch technique. J Physiol. 1984 Feb;347:751–768. doi: 10.1113/jphysiol.1984.sp015094. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Almers W., Stanfield P. R., Stühmer W. Lateral distribution of sodium and potassium channels in frog skeletal muscle: measurements with a patch-clamp technique. J Physiol. 1983 Mar;336:261–284. doi: 10.1113/jphysiol.1983.sp014580. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Almers W., Stirling C. Distribution of transport proteins over animal cell membranes. J Membr Biol. 1984;77(3):169–186. doi: 10.1007/BF01870567. [DOI] [PubMed] [Google Scholar]
- Barish M. E., Thompson S. H. Calcium buffering and slow recovery kinetics of calcium-dependent outward current in molluscan neurones. J Physiol. 1983 Apr;337:201–219. doi: 10.1113/jphysiol.1983.sp014620. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brown A. M., Kunze D. L. Ionic activities in identifiable Aplysia neurons. Adv Exp Med Biol. 1974;50(0):57–73. doi: 10.1007/978-1-4615-9023-1_6. [DOI] [PubMed] [Google Scholar]
- Connor J. A., Stevens C. F. Prediction of repetitive firing behaviour from voltage clamp data on an isolated neurone soma. J Physiol. 1971 Feb;213(1):31–53. doi: 10.1113/jphysiol.1971.sp009366. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eaton D. C. Potassium ion accumulation near a pace-making cell of Aplysia. J Physiol. 1972 Jul;224(2):421–440. doi: 10.1113/jphysiol.1972.sp009903. [DOI] [PMC free article] [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]
- Fiore L., Meunier J. M. Synaptic connections and functional organization in Aplysia buccal ganglia. J Neurobiol. 1979 Jan;10(1):13–29. doi: 10.1002/neu.480100103. [DOI] [PubMed] [Google Scholar]
- Graubard K. Voltage attenuation within Aplysia neurons: the effect of branching pattern. Brain Res. 1975 May 2;88(2):325–332. doi: 10.1016/0006-8993(75)90394-7. [DOI] [PubMed] [Google Scholar]
- Guharay F., Sachs F. Stretch-activated single ion channel currents in tissue-cultured embryonic chick skeletal muscle. J Physiol. 1984 Jul;352:685–701. doi: 10.1113/jphysiol.1984.sp015317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HAGIWARA S., SAITO N. Voltage-current relations in nerve cell membrane of Onchidium verruculatum. J Physiol. 1959 Oct;148:161–179. doi: 10.1113/jphysiol.1959.sp006279. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Horn R. Propagating calcium spikes in an axon of Aplysia. J Physiol. 1978 Aug;281:513–534. doi: 10.1113/jphysiol.1978.sp012437. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kado R. T. Aplysia giant cell: soma-axon voltage clamp current differences. Science. 1973 Nov 23;182(4114):843–845. doi: 10.1126/science.182.4114.843. [DOI] [PubMed] [Google Scholar]
- Mirolli M., Talbott S. R. The geometrical factors determining the electrotonic properties of a molluscan neurone. J Physiol. 1972 Dec;227(1):19–34. doi: 10.1113/jphysiol.1972.sp010017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neher E., Lux H. D. Properties of somatic membrane patches of snail neurons under voltage clamp. Pflugers Arch. 1971;322(1):35–38. doi: 10.1007/BF00586662. [DOI] [PubMed] [Google Scholar]
- Neher E., Lux H. D. Voltage clamp on Helix pomatia neuronal membrane; current measurement over a limited area of the soma surface. Pflugers Arch. 1969;311(3):272–277. doi: 10.1007/BF00590532. [DOI] [PubMed] [Google Scholar]
- Neher E. Two fast transient current components during voltage clamp on snail neurons. J Gen Physiol. 1971 Jul;58(1):36–53. doi: 10.1085/jgp.58.1.36. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Poo M. M. Mobility and localization of proteins in excitable membranes. Annu Rev Neurosci. 1985;8:369–406. doi: 10.1146/annurev.ne.08.030185.002101. [DOI] [PubMed] [Google Scholar]
- Ram J. L., Dagan D. Inactivating and non-inactivating outward current channels in cell-attached patches of Helix neurons. Brain Res. 1987 Mar 3;405(1):16–25. doi: 10.1016/0006-8993(87)90985-1. [DOI] [PubMed] [Google Scholar]
- Siegelbaum S. A., Camardo J. S., Kandel E. R. Serotonin and cyclic AMP close single K+ channels in Aplysia sensory neurones. Nature. 1982 Sep 30;299(5882):413–417. doi: 10.1038/299413a0. [DOI] [PubMed] [Google Scholar]
- Solc C. K., Zagotta W. N., Aldrich R. W. Single-channel and genetic analyses reveal two distinct A-type potassium channels in Drosophila. Science. 1987 May 29;236(4805):1094–1098. doi: 10.1126/science.2437657. [DOI] [PubMed] [Google Scholar]
- Standen N. B. Calcium and sodium ions as charge carriers in the action potential of an identified snail neurone. J Physiol. 1975 Jul;249(2):241–252. doi: 10.1113/jphysiol.1975.sp011013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stewart W. W. Functional connections between cells as revealed by dye-coupling with a highly fluorescent naphthalimide tracer. Cell. 1978 Jul;14(3):741–759. doi: 10.1016/0092-8674(78)90256-8. [DOI] [PubMed] [Google Scholar]
- Strickholm A. Impedance of a Small Electrically Isolated Area of the Muscle Cell Surface. J Gen Physiol. 1961 Jul 1;44(6):1073–1088. doi: 10.1085/jgp.44.6.1073. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Strong J. A., Kaczmarek L. K. Multiple components of delayed potassium current in peptidergic neurons of Aplysia: modulation by an activator of adenylate cyclase. J Neurosci. 1986 Mar;6(3):814–822. doi: 10.1523/JNEUROSCI.06-03-00814.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TAUC L. Identification of active membrane areas in the giant neuron of Aplysia. J Gen Physiol. 1962 Jul;45:1099–1115. doi: 10.1085/jgp.45.6.1099. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TAUC L. Site of origin and propagation in spike in the giant neuron of Aplysia. J Gen Physiol. 1962 Jul;45:1077–1097. doi: 10.1085/jgp.45.6.1077. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Taylor P. S. Selectivity and patch measurements of A-current channels in Helix aspersa neurones. J Physiol. 1987 Jul;388:437–447. doi: 10.1113/jphysiol.1987.sp016623. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson S. H. Three pharmacologically distinct potassium channels in molluscan neurones. J Physiol. 1977 Feb;265(2):465–488. doi: 10.1113/jphysiol.1977.sp011725. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson S., Coombs J. Spatial distribution of Ca currents in molluscan neuron cell bodies and regional differences in the strength of inactivation. J Neurosci. 1988 Jun;8(6):1929–1939. doi: 10.1523/JNEUROSCI.08-06-01929.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson S., Smith S. J., Johnson J. W. Slow outward tail currents in molluscan bursting pacemaker neurons: two components differing in temperature sensitivity. J Neurosci. 1986 Nov;6(11):3169–3176. doi: 10.1523/JNEUROSCI.06-11-03169.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Westerfield M., Lux H. D. Calcium-activated potassium conductance noise in snail neurons. J Neurobiol. 1982 Nov;13(6):507–517. doi: 10.1002/neu.480130606. [DOI] [PubMed] [Google Scholar]