Sheep cardiac sarcoplasmic reticulum calcium‐release channels: modification of conductance and gating by temperature.
- 1 March 1991
- journal article
- Published by Wiley in The Journal of Physiology
- Vol. 434 (1) , 469-488
- https://doi.org/10.1113/jphysiol.1991.sp018481
Abstract
1. The gating and conduction properties of single calcium-release channels of sheep isolated cardiac junctional sarcoplasmic reticulum membranes incorporated into planar phospholipid bilayers were investigated under voltage clamp conditions at temperatures between 4 and 32 degrees C. 2. Single channel conductance was reduced linearly when temperature was decreased from 32 to 5 degrees C with a Q10 value of 1.5 between 10 and 20 degrees C. The apparent activation enthalpy for conductance between 32 and 5 degrees C was 6.16 +/- 1.2 kcal/mol. 3. Cooling the channel increased open probability (Po) when activating cytosolic calcium concentrations were varied within the range 0.1-100 microM. At an activating free calcium concentration of 10 microM, channel Po increased from 0.13 +/- 0.05 at 23 degrees C to 0.69 +/- 0.07 at 5-10 degrees C. 4. At sub-activating calcium concentrations (100 pM) or high concentrations of calcium (greater than or equal to 1000 microM), the calcium-release channel remained closed at 23 degrees C. Cooling the channel under these conditions did not increase Po. 5. Lifetime analysis indicates that with calcium as the sole activating ligand, the cooling-induced increase in Po results from an increase in channel open lifetimes with no significant alteration in the frequency of channel opening. At 23 degrees C, the open and closed lifetime distributions of the calcium-activated channel are best described by two and three exponentials respectively. At reduced temperatures (5-10 degrees C), both open and closed lifetime distributions were best described by three exponentials. 6. At sub-activating calcium concentrations, calcium-independent channel openings could be induced by sulmazole (AR-L 115 BS, 0.5-10 mM). At 23 degrees C, with sulmazole as the sole activating ligand, the best fits to both open and closed lifetime distributions were obtained with three exponentials. At reduced temperatures (5-10 degrees C), Po was increased. Gating was characterized by long open events, however the open and closed lifetime distributions were still best described by three exponentials. 7. The net effect of temperature reduction is an increase in calcium current through the channel. This finding is consistent with the suggestion that calcium release from the SR is a major factor in the initiation of rapid cooling contractures of mammalian cardiac muscle preparations.Keywords
This publication has 43 references indexed in Scilit:
- Divalent cation activation and inhibition of single calcium release channels from sheep cardiac sarcoplasmic reticulum.The Journal of general physiology, 1990
- Sulmazole (AR-L 115BS) activates the sheep cardiac muscle sarcoplasmic reticulum calcium-release channel in the presence and absence of calciumThe Journal of Membrane Biology, 1990
- The cardiac sarcoplasmic reticulum calcium-release channel: modulation of ryanodine binding and single-channel activityBiochimica et Biophysica Acta (BBA) - Biomembranes, 1990
- Modulation of the calcium release channel of sarcoplasmic reticulum by adriamycin and other drugsCell Calcium, 1989
- Evidence for a Ca2+ channel within the ryanodine receptor complex from cardiac sarcoplasmic reticulumBiochemical and Biophysical Research Communications, 1988
- Involvement of dihydropyridine receptors in excitation–contraction coupling in skeletal muscleNature, 1987
- Sarcoplasmic reticulum contains adenine nucleotide-activated calcium channelsNature, 1985
- Inactivation viewed through single sodium channels.The Journal of general physiology, 1984
- The characterization of a monovalent cation-selective channel of mammalian cardiac muscle sarcoplasmic reticulumThe Journal of Membrane Biology, 1984
- Gating kinetics of Ca2+-activated K+ channels from rat muscle incorporated into planar lipid bilayers. Evidence for two voltage-dependent Ca2+ binding reactions.The Journal of general physiology, 1983