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首页> 外文期刊>American Journal of Physiology >Developmental changes in time course of recovery from inactivation in L-type calcium currents of rabbit ventricular myocytes.
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Developmental changes in time course of recovery from inactivation in L-type calcium currents of rabbit ventricular myocytes.

机译:兔心室肌细胞L型钙电流失活恢复时程的发展变化。

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摘要

The mechanisms of recovery from inactivation of the L-type calcium current (I(Ca)) are not well established, and recovery is affected by many experimental conditions. Little is known about developmental changes of recovery from inactivation of I(Ca). We studied developmental changes of recovery from inactivation in I(Ca) using isolated adult and newborn (1-4 days) rabbit ventricular myocytes. We used broken-patch and perforated-patch techniques with physiological extracellular ionic concentrations of calcium and sodium and interpulse conditioning potentials of -80 or -50 mV. We also maximized I(Ca) with forskolin. We found that recovery from inactivation did not differ between adult and newborn cells when either EGTA or BAPTA was used to buffer intracellular calcium. Maximizing I(Ca) with forskolin slowed recovery from inactivation in newborn but not in adult cells. In contrast, when the intracellular buffering of the cell was left nearly intact (perforated patch), recovery from inactivation (half-timeof recovery) in the newborn cells was significantly slower than for the adult cells when either a conditioning potential of -80 mV (140 +/- 9 vs. 58 +/- 4 ms, newborn vs. adu P < 0.05) or -50 mV (641 +/- 106 vs. 168 +/- 15 ms, newborn vs. adu P < 0.05) was used. Forskolin significantly increased half-time of recovery for both adult and newborn cells. Dialysis with no calcium buffer showed a slower recovery from inactivation in newborn cells. Intracellular dialysis with a calcium buffer masked differences in recovery from inactivation of I(Ca) between newborn and adult rabbit ventricular cells.
机译:从L型钙电流(I(Ca))失活中恢复的机制尚未完全确立,并且恢复受许多实验条件的影响。关于I(Ca)失活恢复的发育变化知之甚少。我们研究了使用分离的成年和新生儿(1-4天)兔心室肌细胞从I(Ca)失活中恢复的发展变化。我们使用了具有钙离子和钠离子的生理性细胞外离子浓度以及-80或-50 mV的脉冲间调节电位的破碎补丁和穿孔补丁技术。我们还用毛喉素最大化了I(Ca)。我们发现,当使用EGTA或BAPTA缓冲细胞内钙时,成年和新生细胞之间的失活恢复没有区别。用福司可林使I(Ca)最大化会减慢新生细胞的失活恢复速度,但不会使成年细胞失活。相反,当细胞内缓冲液几乎完好无损(打孔的贴片)时,当条件电位为-80 mV时,新生细胞的失活恢复(恢复时间的一半)比成年细胞明显慢。 140 +/- 9 vs.58 +/- 4 ms,新生儿vs.成人; P <0.05)或-50 mV(641 +/- 106 vs. 168 +/- 15 ms,新生儿vs.成人; P <0.05 )。 Forskolin显着增加了成年和新生细胞的恢复半衰期。没有钙缓冲液的透析显示从新生细胞失活中恢复较慢。用钙缓冲液进行的细胞内透析掩盖了新生和成年兔心室细胞之间因I(Ca)失活而恢复的差异。

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