Bouchard R A, Bose D
Department of Pharmacology & Therapeutics, University of Manitoba, Winnipeg, Canada.
J Gen Physiol. 1992 Jun;99(6):931-60. doi: 10.1085/jgp.99.6.931.
The aim of this work was to determine the relationship between peak twitch amplitude and sarcoplasmic reticulum (SR) Ca2+ content during changes of stimulation frequency in isolated canine ventricle, and to estimate the extent to which these changes were dependent upon sarcolemmal Na(+)-Ca2+ exchange. In physiological [Na+]o, increased stimulation frequency in the 0.2-2-Hz range resulted in a positive inotropic effect characterized by an increase in peak twitch amplitude and a decrease in the duration of contraction, measured as changes in isometric force development or unloaded cell shortening in intact muscle and isolated single cells, respectively. Action potentials recorded from single cells indicated that the inotropic effect was associated with a progressive decrease of action potential duration and a marked reduction in average time spent by the cell near the resting potential during the stimulus train. The frequency-dependent increase of peak twitch force was correlated with an increase of Ca2+ uptake into and release from the SR. This was estimated indirectly using the phasic contractile response to rapid (less than 1 s) lowering of perfusate temperature from 37 degrees C to 0-2 degrees C and changes of twitch amplitude resulting from perturbations in the pattern of electrical stimulation. Lowering [Na+]o from 140 to 70 mM resulted in an increase of contractile strength, which was accompanied by a similar increase of apparent SR Ca2+ content, both of which could be abolished by exposure to ryanodine (1 x 10(-8) M), caffeine (3 x 10(-3) M), or nifedipine (2 x 10(-6) M). Increased stimulation frequency in 70 mM [Na+]o resulted in a negative contractile staircase, characterized by a graded decrease of peak isometric force development or unloaded cell shortening. SR Ca2+ content estimated under identical conditions remained unaltered. Rate constants derived from mechanical restitution studies implied that the depressant effect of increased stimulation frequency in 70 mM [Na+]o was not a consequence of a decreased rate of refilling of a releasable pool of Ca2+ within the cell. These results demonstrate that frequency-dependent changes of contractile strength and intracellular Ca2+ loading in 140 mM [Na+]o require the presence of a functional sarcolemmal Na(+)-Ca2+ exchange process. The possibility that the negative staircase in 70 mM [Na+]o is related to inhibition of Ca(2+)-induced release of Ca2+ from the SR by various cellular mechanisms is discussed.
本研究旨在确定在离体犬心室中,刺激频率改变时峰值抽搐幅度与肌浆网(SR)Ca2+含量之间的关系,并评估这些变化在多大程度上依赖于肌膜Na(+)-Ca2+交换。在生理[Na+]o条件下,0.2-2Hz范围内刺激频率增加导致正性肌力作用,其特征为峰值抽搐幅度增加和收缩持续时间缩短,分别通过完整肌肉中的等长力发展变化或分离的单个细胞中的无负荷细胞缩短来测量。从单个细胞记录的动作电位表明,正性肌力作用与动作电位持续时间的逐渐缩短以及刺激序列期间细胞在静息电位附近花费的平均时间的显著减少有关。峰值抽搐力的频率依赖性增加与Ca2+摄取到SR中以及从SR中释放的增加相关。这是通过对灌注液温度从37℃快速(小于1秒)降至0-2℃的阶段性收缩反应以及电刺激模式扰动引起的抽搐幅度变化间接估计的。将[Na+]o从140 mM降至70 mM导致收缩强度增加,同时表观SR Ca2+含量也有类似增加,两者均可通过暴露于ryanodine(1×10(-8) M)、咖啡因(3×10(-3) M)或硝苯地平(2×10(-6) M)而消除。在70 mM [Na+]o中增加刺激频率导致负性收缩阶梯现象,其特征为峰值等长力发展或无负荷细胞缩短逐渐降低。在相同条件下估计的SR Ca2+含量保持不变。从机械恢复研究得出的速率常数表明,在70 mM [Na+]o中增加刺激频率的抑制作用不是细胞内可释放Ca2+池再填充速率降低的结果。这些结果表明,在140 mM [Na+]o中收缩强度和细胞内Ca2+负荷的频率依赖性变化需要功能性肌膜Na(+)-Ca2+交换过程的存在。讨论了70 mM [Na+]o中的负性阶梯现象是否与各种细胞机制对SR中Ca(2+)诱导的Ca2+释放的抑制有关的可能性。