J Physiol Society Meetings
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Vol 435 pp 349-372
Copyright © 1991 by The Physiological Society
This Article
Right arrow Full Text (PDF)
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wendt-Gallitelli, M F
Right arrow Articles by Isenberg, G
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wendt-Gallitelli, M F
Right arrow Articles by Isenberg, G

Total and free myoplasmic calcium during a contraction cycle: x-ray microanalysis in guinea-pig ventricular myocytes.

M F Wendt-Gallitelli and G Isenberg

Department of Physiology II, University of Tübingen, Germany.

1. At 36 degrees C and 2 mM [Ca2+]o single guinea-pig ventricular myocytes were voltage clamped with patch electrodes. With a paired-pulse protocol applied at 1 Hz, a first pulse to +5 mV was followed by a second pulse to +50 mV. When paired pulsing had potentiated the contraction to the maximum, the cells were shock-frozen for electron-probe microanalysis (EPMA). Shock-freezing was timed at the end of diastole (-80 mV) or at different times during systole (+5 mV). 2. The same paired-pulse protocol was applied to another group of myocytes from which contraction and [Ca2+]i was estimated by microfluospectroscopy (50 microM-Na5-Indo-1). Potentiation moderately reduced diastolic sarcomere length from 1.85 to 1.82 microns and increased diastolic [Ca2+]i from about 95 to 180 nM. In potentiated cells, during the first pulse, contraction peaked within 128 +/- 25 ms after start of depolarization. [Ca2+]i peaked within 25 ms to 890 +/- 220 nM (mean +/- S.E.M.) and fell within 100 ms to about 450 nM. 3. Sigma Camyo, the total calcium concentration in the overlapping myofilaments (A-band), was measured by EPMA in seventeen potentiated myocytes. During diastole, sigma Camyo was 2.6 +/- 0.4 mmol (kg dry weight (DW]-1 which can be converted to 0.65 mM (mmoles per litre myofibrillar space). Since [Ca2+]i was 180 nM, we estimate that 99.97% of total calcium is bound. 4. A time course for systolic sigma Camyo was determined by shock-freezing thirteen cells at different times after start of depolarization to +5 mV. Sigma Camyo was 5.5 +/- 0.3 mmol (kg DW)-1 (1.4 mM) after 15-25 ms, 4.6 +/- 0.5 mmol (kg DW)-1 (1.1 mM) after 30-45 ms, and 3.1 mmol (kg DW)-1 (0.8 mM) after 60-120 ms. The fast time course of sigma Camyo suggests that calcium binds to and unbinds from troponin C at a fast rate. Hence, it is the slow kinetics of the cross-bridges that determines the 130 ms time-to-peak shortening. 5. Mitochondria of potentiated cells contained during diastole a total calcium concentration, sigma Camito, of 1.3 +/- 0.2 mmol (kg DW)-1 (0.4 mM). During the initial 15-25 ms of systole, sigma Camito did not change, however, during 30-45 ms sigma Camito rose to 3.7 +/- 0.5 mmol (kg DW)-1 (1.2 mM). The data suggest that sigma Camito can follow sigma Camyo with some delay, thereby participating in both slow diastolic and fast systolic changes in total calcium (sigma Ca), at least under the given conditions.(ABSTRACT TRUNCATED AT 400 WORDS)




This article has been cited by other articles:


Home page
Physiol. Rev.Home page
H. E. D. J. ter Keurs and P. A. Boyden
Calcium and Arrhythmogenesis
Physiol Rev, April 1, 2007; 87(2): 457 - 506.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
M. Sedova, E. N. Dedkova, and L. A. Blatter
Integration of rapid cytosolic Ca2+ signals by mitochondria in cat ventricular myocytes
Am J Physiol Cell Physiol, November 1, 2006; 291(5): C840 - C850.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
G. Szalai, G. Csordas, B. M. Hantash, A. P. Thomas, and G. Hajnoczky
Calcium Signal Transmission between Ryanodine Receptors and Mitochondria
J. Biol. Chem., May 12, 2000; 275(20): 15305 - 15313.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
Y. Wang, K. Hirai, and M. Ashraf
Activation of Mitochondrial ATP-Sensitive K+ Channel for Cardiac Protection Against Ischemic Injury Is Dependent on Protein Kinase C Activity
Circ. Res., October 15, 1999; 85(8): 731 - 741.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
N. B. Pivovarova, J. Hongpaisan, S. B. Andrews, and D. D. Friel
Depolarization-Induced Mitochondrial Ca Accumulation in Sympathetic Neurons: Spatial and Temporal Characteristics
J. Neurosci., August 1, 1999; 19(15): 6372 - 6384.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
E. Carmeliet
Cardiac Ionic Currents and Acute Ischemia: From Channels to Arrhythmias
Physiol Rev, July 1, 1999; 79(3): 917 - 1017.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
Y. Wang and M. Ashraf
Role of Protein Kinase C in Mitochondrial KATP Channel–Mediated Protection Against Ca2+ Overload Injury in Rat Myocardium
Circ. Res., May 28, 1999; 84(10): 1156 - 1165.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
A. Zaza, M. Rocchetti, A. Brioschi, A. Cantadori, and A. Ferroni
Dynamic Ca2+-Induced Inward Rectification of K+ Current During the Ventricular Action Potential
Circ. Res., May 19, 1998; 82(9): 947 - 956.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
G. C. Sparagna, K. K. Gunter, S.-S. Sheu, and T. E. Gunter
Mitochondrial Calcium Uptake from Physiological-type Pulses of Calcium
J. Biol. Chem., November 17, 1995; 270(46): 27510 - 27515.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
R. A. Bouchard, R. B. Clark, and W. R. Giles
Effects of Action Potential Duration on Excitation-Contraction Coupling in Rat Ventricular Myocytes : Action Potential Voltage-Clamp Measurements
Circ. Res., May 1, 1995; 76(5): 790 - 801.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1991 The Physiological Society.