Chua M, Dulhunty A F
Department of Physiology, John Curtin School of Medical Research, Australian National University, Canberra, A.C.T.
J Gen Physiol. 1988 May;91(5):737-57. doi: 10.1085/jgp.91.5.737.
K contractures and two-microelectrode voltage-clamp techniques were used to measure inactivation of excitation-contraction coupling in small bundles of fibers from rat extensor digitorum longus (e.d.l.) and soleus muscles at 21 degrees C. The rate of spontaneous relaxation was faster in e.d.l. fibers: the time for 120 mM K contractures to decay to 50% of maximum tension was 9.8 +/- 0.5 s (mean +/- SEM) in e.d.l. and 16.8 +/- 1.7 s in soleus. The rate of decay depended on membrane potential: in e.d.l., the 50% decay time was 14.3 +/- 0.7 s for contractures in 80 mM K (Vm = 25 mV) and 4.9 +/- 0.4 s in 160 mM K (Vm = -3 mV). In contrast to activation, which occurred with less depolarization in soleus fibers, steady state inactivation required more depolarization: after 3 min at -40 mV in 40 mM K, the 200 mM K contracture amplitude in e.d.l. fell to 28 +/- 10% (n = 5) of control, but remained at 85 +/- 2% (n = 6) of control in soleus. These different inactivation properties in e.d.l. and soleus fibers were not influenced by the fact that the 200 mM K solution used to test for steady state inactivation produced contractures that were maximal in soleus fibers but submaximal in e.d.l.: a relatively similar depression was recorded in maximal (200 mM K) and submaximal (60 and 80 mM K) contracture tension. A steady state "pedestal" of tension was observed with maintained depolarization after K contracture relaxation and was larger in soleus than in e.d.l. fibers. The pedestal tension was attributed to the overlap between the activation and inactivation curves for tension vs. membrane potential, which was greater in soleus than in e.d.l. fibers. The K contracture results were confirmed with the two-microelectrode voltage clamp: the contraction threshold increased to more positive potentials at holding potentials of -50 mV in e.d.l. or -40 mV in soleus. At holding potentials of -30 mV in e.d.l. or 0 mV in soleus, contraction could not be evoked by 15-ms pulses to +20 mV. Both K contracture and voltage-clamp experiments revealed that activation in soleus fibers occurred with a smaller transient depolarization and was maintained with greater steady state depolarization than in e.d.l. fibers. The K contracture and voltage-clamp results are described by a model in which contraction depends on the formation of a threshold concentration of activator from a voltage-sensitive molecule that can exist in the precursor, activator, or inactive states.
采用K收缩和双微电极电压钳技术,在21℃下测量大鼠趾长伸肌(e.d.l.)和比目鱼肌小纤维束中兴奋 - 收缩偶联的失活情况。e.d.l.纤维的自发松弛速率更快:120 mM K收缩至最大张力的50%所需时间,e.d.l.为9.8±0.5秒(平均值±标准误),比目鱼肌为16.8±1.7秒。衰减速率取决于膜电位:在e.d.l.中,80 mM K(Vm = 25 mV)收缩时50%衰减时间为14.3±0.7秒,160 mM K(Vm = -3 mV)时为4.9±0.4秒。与激活不同,比目鱼肌纤维激活时去极化程度较小,而稳态失活需要更大程度的去极化:在40 mM K中 - 40 mV保持3分钟后,e.d.l.中200 mM K收缩幅度降至对照的28±10%(n = 5),但比目鱼肌仍保持在对照的85±2%(n = 6)。用于测试稳态失活的200 mM K溶液在比目鱼肌纤维中产生的收缩为最大,而在e.d.l.中为次最大,这一事实并未影响e.d.l.和比目鱼肌纤维这些不同的失活特性:在最大(200 mM K)和次最大(60和80 mM K)收缩张力中记录到相对相似的降低。在K收缩松弛后保持去极化时观察到张力的稳态“基座”,比目鱼肌中的比e.d.l.纤维中的更大。基座张力归因于张力与膜电位的激活和失活曲线之间的重叠,比目鱼肌中的重叠比e.d.l.纤维中的更大。K收缩结果通过双微电极电压钳得到证实:在e.d.l.中 - 50 mV或比目鱼肌中 - 40 mV的钳制电位下,收缩阈值向更正电位增加。在e.d.l.中 - 30 mV或比目鱼肌中0 mV的钳制电位下,15毫秒 + 20 mV脉冲不能诱发收缩。K收缩和电压钳实验均表明,与e.d.l.纤维相比,比目鱼肌纤维激活时的瞬时去极化较小,且在更大的稳态去极化下维持。K收缩和电压钳结果由一个模型描述,其中收缩取决于由一种电压敏感分子形成阈值浓度的激活剂,该分子可以以前体、激活剂或失活状态存在。