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Properties of the low threshold Ca current in single frog atrial cardiomyocytes. A comparison with the high threshold Ca current

机译:蛙蛙心房心肌细胞低阈值Ca电流的特性。与高阈值Ca电流的比较

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摘要

The properties of the low threshold Ca current (ICaT) in bullfrog (Rana catesbeiana) isolated atrial cardiomyocytes were studied using the whole-cell recording patch-clamp technique and compared with those of the high threshold Ca current (ICaL). In 91% of atrial cells we observed both ICaT and ICaL when collagenase and trypsin were used to dissociate the cells. But when pronase was used, only 30% of the cells exhibited ICaT. ICaT was never found in ventricular cells. ICaT could be investigated more easily when ICaL was inhibited by Cd ions (50 microM). Its kinetics were unchanged by substituting Ba for Ca, or in the presence of high concentrations of Ba. Both ICaT and ICaL exhibited reduced inactivation after high depolarizing prepulses. ICaT was found to be sensitive to dihydropyridines: 1 microM nifedipine decreased this current while 1 microM BAY K 8644 increased it; this occurred without significant variations in the steady-state inactivation curve. ICaT was more sensitive than ICaL to alpha 1-adrenergic and P2-purinergic stimulations, while ICaL was more sensitive to beta-adrenergic stimulation. Isoproterenol was still able to increase ICaT in the presence of high intracellular cAMP. Both currents were increased by 1 microM ouabain (although ICaL only transiently) and decreased by 10 microM ouabain. It is concluded that the two types of Ca channels can be observed in bullfrog atrial cells and that they are specifically altered by pharmacological agents and neuromediators. This may have implications for cardiac behavior.
机译:使用全细胞记录膜片钳技术研究了牛蛙(Rana catesbeiana)分离的心房心肌细胞中低阈值Ca电流(ICaT)的特性,并与高阈值Ca电流(ICaL)进行了比较。当使用胶原酶和胰蛋白酶解离细胞时,在91%的心房细胞中我们同时观察到ICaT和ICaL。但是当使用链酶时,只有30%的细胞表现出ICaT。从未在心室细胞中发现ICaT。当ICaL被Cd离子(50 microM)抑制时,可以更容易地研究ICaT。用Ba代替Ca或在高浓度Ba的存在下其动力学没有变化。高去极化预脉冲后,ICaT和ICaL均显示出减少的失活。发现ICaT对二氢吡啶敏感:1 microM硝苯地平降低了该电流,而1 microM BAY K 8644增加了该电流;稳态失活曲线没有明显变化。与α1肾上腺素能和P2嘌呤能刺激相比,ICaT比ICaL更敏感,而对β-肾上腺素能刺激更敏感。在高细胞内cAMP存在下,异丙肾上腺素仍能够增加ICaT。两种电流都增加了1 microM哇巴因(尽管只是短暂的ICaL)而减少了10 microM哇巴因。结论是,在牛蛙心房细胞中可以观察到两种类型的Ca通道,并且它们被药理剂和神经介质特异性地改变了。这可能对心脏行为有影响。

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