A new integrative method to quantify total Ca2+ handling and futile Ca2+ cycling in failing hearts

被引:23
作者
Shimizu, J
Araki, J
Mizuno, J
Lee, S
Syuu, Y
Hosogi, S
Mohri, S
Mikane, T
Takaki, M
Taylor, TW
Suga, H [1 ]
机构
[1] Okayama Univ, Sch Med, Dept Physiol 2, Okayama 7008558, Japan
[2] Nara Med Univ, Dept Physiol 2, Kashihara, Nara 6348521, Japan
[3] SE Texas Med Associates, Beaumont, TX 77702 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1998年 / 275卷 / 06期
关键词
excitation-contraction coupling; contractility; postextrasystolic potentiation; sarcoplasmic reticulum; ryanodine;
D O I
10.1152/ajpheart.1998.275.6.H2325
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ca2+ handling in excitation-contraction coupling requires considerable O-2 consumption (VO2) in cardiac contraction. We have developed an integrative method to quantify total Ca2+ handling in normal hearts. However, its direct application to failing hearts, where futile Ca2+ cycling via the Ca2+-leaky sarcoplasmic reticulum (SR) required an increased Ca2+ handling VO2, was not legitimate. To quantify total Ca2+ handling even in such failing hearts, we combined futile Ca2+ cycling with Ca2+ handling VO2 and the internal Ca2+ recirculation fraction via the SR. We applied this method to the canine heart mechanoenergetics before and after intracoronary ryanodine at nanomolar concentrations. We found that total Ca2+ handling per beat was halved after the ryanodine treatment from similar to 60 mu mol/kg left ventricle before ryanodine. We also found that futile Ca2+ cycling via the SR increased to >1 cycle/beat after ryanodine from presumably zero before ryanodine. These results support the applicability of the present method to the failing hearts with futile Ca2+ cycling via the SR.
引用
收藏
页码:H2325 / H2333
页数:9
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