Cota G, Nicola Siri L, Stefani E
J Physiol. 1983 May;338:395-412. doi: 10.1113/jphysiol.1983.sp014679.
Voltage-clamp experiments using the three micro-electrode method were performed to study the temperature dependence of the calcium current ICa in intact twitch skeletal muscle fibres of the frog. Contraction was blocked by recording in hypertonic sucrose solutions. For depolarizations smaller than 0 mV the decay of the transient, slow, inward current, recorded in the presence of external tetraethylammonium (TEA+) and by replacing Cl- for CH3SO3-, followed a complex time course. For larger depolarizations, after the initial inward current, there was a prominent, slow, outward current which showed two phases: after reaching a peak (time to peak 1.0 sec, peak amplitude 20-50 microA/cm2 at 20 mV) it slowly declined to a steady level in about 2-3 sec at 23 degrees C. The inward current was greatly reduced or abolished by the adding of 2 mM-Cd2+ or by replacing external Ca2+ with Mg2+. The amplitude and time course of slow, outward currents were not obviously modified by replacing Ca2+ with Mg2+, having the two described phases. However, in the presence of Cd2+ the first transient phase of the outward current was not detected and only outward currents slowly increasing to a steady level were observed. Reliable ICa records were obtained by further blocking K+ outward currents by incubating the muscles in a K+-free TEA+- and Cs+-containing solution prior to experiments. Tubular space clamp was improved by recording ICa from small fibres with 20-30 microns radius. The decay phase of ICa under a maintained depolarization in incubated muscles was fitted by a single exponential. The corresponding rate constant determined between 12 and 24 degrees C strongly depended on temperature, as expected for a gating process. The values for the activation energy and the corresponding Q10 (calculated for a 10-20 degrees C transition) were respectively: 17.5 +/- 1.0 kcal/mole and 2.9 +/- 0.2 at 0 mV, and 18.0 +/- 1.5 kcal/mole and 3.0 +/- 0.3 at -20 mV. The activation phase of ICa, analysed following the m alpha h Hodgkin-Huxley kinetic model, showed a similar temperature dependence with a Q10 of 3.0 +/- 0.3. The peak amplitude of ICa and the limiting Ca2+ permeability had a lower Q10 value of about 1.6. For a given temperature the rate constant of decay was independent of ICa peak amplitude in disagreement with a current-dependent process (intratubular Ca2+ depletion or intracellular Ca2+ accumulation) for the decay of ICa. In conclusion, our results favour a gating process (inactivation) as the principal mechanism underlying the decay phase of ICa under a maintained depolarization.
采用三微电极法进行电压钳实验,以研究青蛙完整单收缩骨骼肌纤维中钙电流ICa的温度依赖性。在高渗蔗糖溶液中记录时收缩被阻断。对于小于0 mV的去极化,在存在外部四乙铵(TEA+)并将Cl-替换为CH3SO3-的情况下记录到的瞬时、缓慢内向电流的衰减遵循复杂的时间进程。对于更大的去极化,在初始内向电流之后,有一个显著的、缓慢的外向电流,它呈现两个阶段:在达到峰值后(在20 mV时,峰值时间为1.0秒,峰值幅度为20 - 50 μA/cm2),它在23℃下约2 - 3秒内缓慢下降至稳定水平。加入2 mM - Cd2+或用Mg2+替换外部Ca2+可使内向电流大大降低或消除。用Mg2+替换Ca2+时,缓慢外向电流的幅度和时间进程没有明显改变,仍有所述的两个阶段。然而,在存在Cd2+的情况下,未检测到外向电流的第一个瞬态阶段,仅观察到外向电流缓慢增加至稳定水平。在实验前将肌肉置于无K+、含TEA+和Cs+的溶液中孵育,通过进一步阻断K+外向电流获得了可靠的ICa记录。通过记录半径为20 - 30微米的小纤维的ICa,改进了管状空间钳。孵育肌肉在持续去极化下ICa的衰减相由单指数拟合。在12至24℃之间确定的相应速率常数强烈依赖于温度,这对于一个门控过程是预期的。活化能和相应的Q10值(针对10 - 20℃的转变计算)分别为:在0 mV时为17.5±1.0 kcal/mol和2.9±0.2,在 - 20 mV时为18.0±1.5 kcal/mol和3.0±0.3。按照mαh霍奇金 - 赫胥黎动力学模型分析的ICa活化相显示出类似的温度依赖性,Q10为3.0±0.