Literature DB >> 2561792

Single sodium channels from canine ventricular myocytes: voltage dependence and relative rates of activation and inactivation.

M F Berman1, J S Camardo, R B Robinson, S A Siegelbaum.   

Abstract

1. Single sodium channel currents were recorded from canine ventricular myocytes in cell-attached patches. The relative rates of single-channel activation vs. inactivation as well as the voltage dependence of the rate of open-channel inactivation were studied. 2. Ensemble-averaged sodium currents showed relatively normal activation and inactivation kinetics, although the mid-point of the steady-state inactivation (h infinity) curve was shifted by 20-30 mV in the hyperpolarizing direction. This shift was due to the bath solution, which contained isotonic KCl to depolarize the cell to 0 mV. 3. Steady-state activation showed less of a voltage shift. The threshold for eliciting channel opening was around -70 mV and the mid-point of activation occurred near -50 mV. 4. The decline of the ensemble-averaged sodium current during a maintained depolarization was fitted by a single exponential function characterizing the apparent time constant of inactivation (tau h). The apparent rate of inactivation was voltage dependent, with tau h decreasing e-fold for a 15.4 mV depolarization. 5. The relative contributions of the rates of single-channel activation and inactivation in determining the time course of current decay (tau h) were examined using the approach of Aldrich, Corey & Stevens (1983). Mean channel open time (tau o) showed significant voltage dependence, increasing from 0.5 ms at -70 mV to around 0.8 ms at -40 mV. At -70 mV tau h was much greater than tau o, while at -40 mV the two time constants were similar. 6. The degree to which the kinetics of single-channel activation contribute to tau h was studied using the first latency distribution. The first latency function was fitted by two exponentials. The slow component was voltage dependent, decreasing from 19 ms at -70 mV to 0.5 ms at -40 mV. The fast component (0.1-0.5 ms) was not well resolved. 7. Comparing the first latency distribution with the time course of the ensemble-averaged sodium current at -40 mV showed that activation is nearly complete by the time of peak inward sodium current. However, at -70 mV, activation overlaps significantly with the apparent time course of inactivation of the ensemble-averaged current. 8. Using the methods of Aldrich et al. (1983) we also measured the apparent rate of open-channel closing (a) and open-channel inactivation (b). Both rates were voltage dependent, with a showing an e-fold decrease for an 11 mV depolarization and b showing an e-fold increase for a 30 mV depolarization.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1989        PMID: 2561792      PMCID: PMC1189189          DOI: 10.1113/jphysiol.1989.sp017734

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  26 in total

1.  Modified gating behaviour of aconitine treated single sodium channels from adult cardiac myocytes.

Authors:  B Nilius; K Benndorf; F Markwardt
Journal:  Pflugers Arch       Date:  1986-12       Impact factor: 3.657

Review 2.  New studies of the excitatory sodium currents in heart muscle.

Authors:  H A Fozzard; C T January; J C Makielski
Journal:  Circ Res       Date:  1985-04       Impact factor: 17.367

3.  Isolated myocytes from adult canine left ventricle: Ca2+ tolerance, electrophysiology, and ultrastructure.

Authors:  K Hewett; M J Legato; P Danilo; R B Robinson
Journal:  Am J Physiol       Date:  1983-11

4.  Unitary sodium channels in isolated cardiac myocytes of rabbit.

Authors:  A O Grant; C F Starmer; H C Strauss
Journal:  Circ Res       Date:  1983-12       Impact factor: 17.367

5.  Statistical analysis of single sodium channels. Effects of N-bromoacetamide.

Authors:  R Horn; C A Vandenberg; K Lange
Journal:  Biophys J       Date:  1984-01       Impact factor: 4.033

6.  Existence of distinct sodium channel messenger RNAs in rat brain.

Authors:  M Noda; T Ikeda; T Kayano; H Suzuki; H Takeshima; M Kurasaki; H Takahashi; S Numa
Journal:  Nature       Date:  1986 Mar 13-19       Impact factor: 49.962

7.  Statistical properties of single sodium channels.

Authors:  R Horn; C A Vandenberg
Journal:  J Gen Physiol       Date:  1984-10       Impact factor: 4.086

8.  Inactivation viewed through single sodium channels.

Authors:  C A Vandenberg; R Horn
Journal:  J Gen Physiol       Date:  1984-10       Impact factor: 4.086

9.  Slow currents through single sodium channels of the adult rat heart.

Authors:  J B Patlak; M Ortiz
Journal:  J Gen Physiol       Date:  1985-07       Impact factor: 4.086

10.  Cardiac Na currents and the inactivating, reopening, and waiting properties of single cardiac Na channels.

Authors:  D L Kunze; A E Lacerda; D L Wilson; A M Brown
Journal:  J Gen Physiol       Date:  1985-11       Impact factor: 4.086

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  25 in total

1.  Cardiac sodium channel Markov model with temperature dependence and recovery from inactivation.

Authors:  L A Irvine; M S Jafri; R L Winslow
Journal:  Biophys J       Date:  1999-04       Impact factor: 4.033

2.  Role of the C-terminal domain in inactivation of brain and cardiac sodium channels.

Authors:  M Mantegazza; F H Yu; W A Catterall; T Scheuer
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-11       Impact factor: 11.205

3.  A multi-modal composition of the late Na+ current in human ventricular cardiomyocytes.

Authors:  Victor A Maltsev; Albertas I Undrovinas
Journal:  Cardiovasc Res       Date:  2005-10-11       Impact factor: 10.787

4.  The quantal gating charge of sodium channel inactivation.

Authors:  N G Greeff; I C Forster
Journal:  Eur Biophys J       Date:  1991       Impact factor: 1.733

5.  Sodium channel inactivation from resting states in guinea-pig ventricular myocytes.

Authors:  J H Lawrence; D T Yue; W C Rose; E Marban
Journal:  J Physiol       Date:  1991-11       Impact factor: 5.182

6.  Time-dependent molecular memory in single voltage-gated sodium channel.

Authors:  Tapan K Nayak; S K Sikdar
Journal:  J Membr Biol       Date:  2007-09-01       Impact factor: 1.843

7.  Remodeling in cells from different regions of the reentrant circuit during ventricular tachycardia.

Authors:  Shigeo Baba; Wen Dun; Candido Cabo; Penelope A Boyden
Journal:  Circulation       Date:  2005-10-03       Impact factor: 29.690

8.  Maximum open probability of single Na+ channels during depolarization in guinea-pig cardiac cells.

Authors:  T Kimitsuki; T Mitsuiye; A Noma
Journal:  Pflugers Arch       Date:  1990-07       Impact factor: 3.657

9.  Voltage clamp of the cardiac sodium current at 37 degrees C in physiologic solutions.

Authors:  K T Murray; T Anno; P B Bennett; L M Hondeghem
Journal:  Biophys J       Date:  1990-03       Impact factor: 4.033

10.  Modelling the activation, opening, inactivation and reopening of the voltage-gated sodium channel.

Authors:  R D Keynes; F Elinder
Journal:  Proc Biol Sci       Date:  1998-02-22       Impact factor: 5.349

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