Fig. 1 (A) Average current voltage relations of peak I<sub>Na</sub> in Con (n=10), nAF (n=7) and cAF (n=9) cells using protocol shown on left. (B) Average.

Slides:



Advertisements
Similar presentations
Date of download: 7/9/2016 Copyright © The American College of Cardiology. All rights reserved. Electrical remodeling in hearts from a calcium-dependent.
Advertisements

Sarcolemmal Ca2+-entry through L-type Ca2+ channels controls the profile of Ca2+- activated Cl− current in canine ventricular myocytes  Balázs Horváth,
Fig. 1 Inhibition of hERG channels by bisindolylmaleimide I
M. Martini, M.L. Rossi, G. Rubbini, G. Rispoli  Biophysical Journal 
Teresa K. Aman, Indira M. Raman  Biophysical Journal 
Binding Site in Eag Voltage Sensor Accommodates a Variety of Ions and is Accessible in Closed Channel  William R. Silverman, John P.A. Bannister, Diane.
Christian Rosenmund, Charles F Stevens  Neuron 
Volume 80, Issue 2, Pages (February 2001)
Volume 32, Issue 6, Pages (December 2001)
Rundown of the Hyperpolarization-Activated KAT1 Channel Involves Slowing of the Opening Transitions Regulated by Phosphorylation  Xiang D. Tang, Toshinori.
Volume 44, Issue 3, Pages (October 2004)
Tony L. Creazzo, Jarrett Burch, Robert E. Godt  Biophysical Journal 
Differential Modulation of Cardiac Ca2+ Channel Gating by β-Subunits
Altered Subthreshold Sodium Currents and Disrupted Firing Patterns in Purkinje Neurons of Scn8a Mutant Mice  Indira M Raman, Leslie K Sprunger, Miriam.
FPL Modification of CaV1
Victor G. Romanenko, George H. Rothblat, Irena Levitan 
Zhuren Wang, J. Christian Hesketh, David Fedida  Biophysical Journal 
Volume 77, Issue 4, Pages (October 1999)
Thomas Voets, Erwin Neher, Tobias Moser  Neuron 
Unitary Conductance Variation in Kir2
Volume 74, Issue 1, Pages (January 1998)
Mechanosensitivity of N-Type Calcium Channel Currents
A. Dinse, K.J. Fo¨hr, M. Georgieff, C. Beyer, A. Bulling, H.U. Weigt 
Kristian Wadel, Erwin Neher, Takeshi Sakaba  Neuron 
David Zenisek, Gary Matthews  Neuron 
Volume 11, Issue 1, Pages (January 2014)
Volume 106, Issue 12, Pages (June 2014)
The Reduced Release Probability of Releasable Vesicles during Recovery from Short- Term Synaptic Depression  Ling-Gang Wu, J.Gerard G Borst  Neuron  Volume.
Volume 14, Issue 11, Pages (November 2017)
Efficacy of Thalamocortical and Intracortical Synaptic Connections
Volume 9, Issue 4, Pages (November 2014)
Volume 32, Issue 6, Pages (December 2001)
A Computational Model of the Human Left-Ventricular Epicardial Myocyte
International Journal of Cardiology
K. Purtell, K.J. Gingrich, W. Ouyang, K.F. Herold, Hemmings H.C.  
Brian Chu, Marten Postma, Roger C. Hardie  Biophysical Journal 
Teresa K. Aman, Indira M. Raman  Biophysical Journal 
Maarten H.P. Kole, Johannes J. Letzkus, Greg J. Stuart  Neuron 
Volume 20, Issue 4, Pages (April 1998)
Carlos A. Obejero-Paz, Stephen W. Jones, Antonio Scarpa 
Ca2+- and Voltage-Dependent Gating of Ca2+- and ATP-Sensitive Cationic Channels in Brain Capillary Endothelium  László Csanády, Vera Adam-Vizi  Biophysical.
Katie C. Bittner, Dorothy A. Hanck  Biophysical Journal 
Volume 16, Issue 3, Pages (March 1996)
Timothy Mickus, Hae-yoon Jung, Nelson Spruston  Biophysical Journal 
Rapid and Slow Voltage-Dependent Conformational Changes in Segment IVS6 of Voltage-Gated Na+ Channels  Vasanth Vedantham, Stephen C. Cannon  Biophysical.
Volume 93, Issue 12, Pages (December 2007)
Heteromultimeric Interactions among K+ Channel Subunits from Shaker and eag Families in Xenopus Oocytes  Mai-Lei Chen, Toshinori Hoshi, Chun-Fang Wu 
Volume 100, Issue 1, Pages (January 2011)
Samuel J. Goodchild, Logan C. Macdonald, David Fedida 
Volume 101, Issue 4, Pages (August 2011)
Effects of Temperature on Heteromeric Kv11.1a/1b and Kv11.3 Channels
Strong G-Protein-Mediated Inhibition of Sodium Channels
Effects of articaine on action potential characteristics and the underlying ion currents in canine ventricular myocytes  A. Szabó, N. Szentandrássy, P.
Phospholemman Modulates the Gating of Cardiac L-Type Calcium Channels
Dendritically Released Peptides Act as Retrograde Modulators of Afferent Excitation in the Supraoptic Nucleus In Vitro  Samuel B Kombian, Didier Mouginot,
A Point Mutation in Domain 4-Segment 6 of the Skeletal Muscle Sodium Channel Produces an Atypical Inactivation State  John P. O’Reilly, Sho-Ya Wang, Ging.
Don E. Burgess, Oscar Crawford, Brian P. Delisle, Jonathan Satin 
Electroporation of DC-3F Cells Is a Dual Process
Inwardly Rectifying Current-Voltage Relationship of Small-Conductance Ca2+-Activated K+ Channels Rendered by Intracellular Divalent Cation Blockade  Heun.
Kinetics of P2X7 Receptor-Operated Single Channels Currents
Volume 16, Issue 4, Pages (April 2019)
Daniel Bakowski, Anant B. Parekh  Current Biology 
Christian Rosenmund, Charles F Stevens  Neuron 
Volume 49, Issue 3, Pages (February 2006)
R.P. Schuhmeier, B. Dietze, D. Ursu, F. Lehmann-Horn, W. Melzer 
Use Dependence of Heat Sensitivity of Vanilloid Receptor TRPV2
Desdemona Fricker, Richard Miles  Neuron 
Byung-Chang Suh, Karina Leal, Bertil Hille  Neuron 
David Naranjo, Hua Wen, Paul Brehm  Biophysical Journal 
Volume 108, Issue 5, Pages (March 2015)
Presentation transcript:

Fig. 1 (A) Average current voltage relations of peak I<sub>Na</sub> in Con (n=10), nAF (n=7) and cAF (n=9) cells using protocol shown on left. (B) Average current density relations of peak I<sub>Na</sub> in Con, nAF and cAF cells. *P<0.05 nAF, cAF versus Con. (C,D) Capacitance-subtracted peak I<sub>Na</sub> in a typical Con and cAF cell. Holding potential, −100 mV. From: Density and function of inward currents in right atrial cells from chronically fibrillating canine atria Cardiovasc Res. 2002;54(2):405-415. doi:10.1016/S0008-6363(02)00279-1 Cardiovasc Res | Copyright © 2002, European Society of Cardiology

Fig. 3 (A) Currents tracings in Con (a), nAF (b), and cAF (c) cell under conditions of these experiments: Ca<sup>2+</sup> 3 mM–EGTAi 10 mM; ryanodine 2 μM; holding voltage, −70 mV to various test voltages. Arrow indicates zero current level. (B) Average peak I<sub>CaL</sub> density in Con (n=25), nAF (n=11) and cAF (n=6) cells. *P<0.05 versus Con. All data collected at same time after establishing whole cell configuration (Con, 15.0±0.5 min; nAF, 16.5±0.7 min; and cAF, 17.5±0.8 min P>0.05). (C) Average first and second time constants (τ<sub>1</sub> and τ<sub>2</sub>) of decay of peak I<sub>CaL</sub> in all cells of the three groups. A<sub>1</sub>/A<sub>total</sub> were 0.75±0.02, 0.79±0.03, 0.76±0.04 in Con, nAF and cAF cells, respectively (P>0.05). Inset shows first 150 ms of tracings from Con, nAF and cAF cells, each normalized to peak and superimposed to illustrate time course of peak current decay. From: Density and function of inward currents in right atrial cells from chronically fibrillating canine atria Cardiovasc Res. 2002;54(2):405-415. doi:10.1016/S0008-6363(02)00279-1 Cardiovasc Res | Copyright © 2002, European Society of Cardiology

Fig. 6 (A) The fraction of current remaining at the end of the clamp step (I<sub>250</sub>) normalized to the peak current (I<sub>max</sub>) for peak Ba<sup>2+</sup> currents in the three different groups. Height of bar denotes average I<sub>250</sub> normalized to I<sub>max</sub>. I<sub>250</sub>/I<sub>max</sub> is significantly less in cAF group when compared to either Con or nAF values suggesting that Ba<sup>2+</sup> current decay is accelerated in cAF cells (see Fig. 5C). (B) The average I<sub>250</sub>/I<sub>max</sub> for several test voltages (V<sub>t</sub>) under these same recording conditions for cells in each group. P<0.05 cAF versus Con curve. From: Density and function of inward currents in right atrial cells from chronically fibrillating canine atria Cardiovasc Res. 2002;54(2):405-415. doi:10.1016/S0008-6363(02)00279-1 Cardiovasc Res | Copyright © 2002, European Society of Cardiology

Fig. 5 (A) Currents tracings in Con (a), nAF (b), and cAF (c) cell under conditions of these experiments; Ba<sup>2+</sup> 3 mM/BAPTAi 10 mM; ryanodine, holding voltage, −70 mV to various test voltages. Arrow indicates zero current. (B) Average peak I<sub>BaL</sub> density voltage relations in Con (n=16), nAF (n=5) and cAF (n=12) cells. Data were all obtained at same time after establishing whole cell configuration (Con, 18.53±0.58 min, nAF, 19.8±1.2 min and cAF 17.9±0.5 min). Note that Con and nAF have comparable peak I<sub>BaL</sub> densities under Ba<sup>2+</sup>/BAPTA conditions while cAF density remains different from Con and nAF. *P<0.05 cAF versus Con, nAF. (C) Typical Con, nAF and cAF peak I<sub>BaL</sub> tracings under Ba<sup>2+</sup>/BAPTA conditions. Each has been normalized and superimposed to emphasize the differences in current decay between cells from the different groups. Note that the small Ba<sup>2+</sup> currents of cAF cells decay more completely during the step depolarization. In (D) the bar graph illustrates the average time for peak current decay to T<sub>0.8max</sub>, T<sub>0.7max</sub>, T<sub>0.6max</sub>, for cells in each group. *P<0.05 Con versus cAF, **P<0.05 nAF versus cAF. Note one Con cell never decayed to 0.6 max during the step depolarization and therefore its value was not included in average at T<sub>0.6max</sub>. From: Density and function of inward currents in right atrial cells from chronically fibrillating canine atria Cardiovasc Res. 2002;54(2):405-415. doi:10.1016/S0008-6363(02)00279-1 Cardiovasc Res | Copyright © 2002, European Society of Cardiology

Fig. 2 Time course of recovery from inactivation of I<sub>Na</sub> using the protocol shown in inset (B). (A) Recovery for cells in Con, nAF and cAF. I<sub>Na</sub> at a certain interpulse interval (IPI) is normalized to I<sub>max</sub> (at IPI=3000 ms) and plotted against IPI. (B) Average recovery curves for all groups for short IPIs. Note the slow recovery at short IPIs in both nAF and cAF cells. *P<0.05 Con versus nAF or Con versus cAF. From: Density and function of inward currents in right atrial cells from chronically fibrillating canine atria Cardiovasc Res. 2002;54(2):405-415. doi:10.1016/S0008-6363(02)00279-1 Cardiovasc Res | Copyright © 2002, European Society of Cardiology

Fig. 4 (A) Currents tracings in Con (a), nAF (b), and cAF (c) cell under conditions of these experiments; Ba<sup>2+</sup> 3 mM–EGTAi 10 mM, ryanodine 2 μM; holding voltage, −70 mV to various test voltages. Arrow indicates zero current. (B) Inset shows peak I<sub>BaL</sub> tracings during step depolarization in a Con, nAF and cAF cell each normalized to peak and superimposed to illustrate differences in current decay in cells of each group. Bar graph illustrates the average time for current decay to 80, 70, 60 and 50% maximum (T<sub>0.8max</sub>, T<sub>0.7max</sub>, T<sub>0.6max</sub>, T<sub>0.5max</sub>, respectively) for Con (n=6), nAF (n=5), cAF(n=7). There were no significant differences among groups. (C) Fraction of Ba<sup>2+</sup> current remaining at I<sub>250</sub> normalized to I<sub>max</sub> current for cells of the three groups. Height of bar denotes average value for each of three groups. There was no significant difference in I<sub>250</sub>/I<sub>max</sub> of peak currents under these recording conditions even though peak current densities differed. From: Density and function of inward currents in right atrial cells from chronically fibrillating canine atria Cardiovasc Res. 2002;54(2):405-415. doi:10.1016/S0008-6363(02)00279-1 Cardiovasc Res | Copyright © 2002, European Society of Cardiology