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Inhibition of pacemaker current by the bradycardic agent ZD 7288 is lost use-dependently in sheep cardiac Purkinje fibres.

作者信息

Berger F, Borchard U, Gelhaar R, Hafner D, Weis T M

机构信息

Institut für Pharmakologie, Heinrich-Heine-Universität Düesseldorf, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1995 Dec;353(1):64-72. doi: 10.1007/BF00168917.

DOI:10.1007/BF00168917
PMID:8750918
Abstract

The inhibition of the pacemaker current (if) in sheep cardiac Purkinje fibers by ZD 7288 [4-(N-ethyl-N-phenylamino)-1,2-dimethyl-6-(methylamino)pyrimidinium++ + chloride] is lost use-dependently. This disinhibition of if was investigated by using the two-microelectrode voltage-clamp technique. The pulse protocol consisted of a rest period (holding potential of about -50 mV, 1-10 micromol/l ZD 7288) followed by a train of test pulses (potential negative to -100 mV, stimulation frequency 0.05 Hz). At the beginning of the first test pulse there was an immediate reduction of if but inhibition was lost during continued stimulation. Activation of if is sigmoidal and the early delay in current activation was prolonged from 33 ms (no ZD 7288) to 424 ms (10 micromol/l ZD 7288). Therefore hardly any disinhibition occurred during short test pulses (0.5s). During longer test pulses (5 s, -120 mV, 10 micromol/l) disinhibition developed with a time constant of about 2 s. The inhibition of if by ZD 7288 was lost voltage-dependently. With 10 micro mol/l ZD 7288 the half-maximal disinhibition occurred at -92 mV and the slope factor of the disinhibition/voltage curve (Boltzmann relation) was 4.8 mV. The voltage-dependent disinhibition could be abolished largely by extracellular application of protease (0.5 mg/ml, 7 min). After prior disinhibition, reinhibition at the holding potential (about -50 mV) followed a bi-exponential time course indicating that inhibition may be produced by a fast (tau=0.7 min) and a slow component (tau=20-30 min). Increasing ZD 7288 concentration from 1 to 10 mu mol/l accelerated reinhibition, mainly by an increase of the amplitude (A) of the fast component. The ratio Afast/Aslow was 0.399 at 1 micromol/l and 2.65 at 10 micromol/l ZD 7288. The reinhibition of if was unchanged by shifting the holding potential from -50 mV to -20 mV. Trials to wash out the effects of 10 micromol/l ZD 7288 gave two results. The inhibition of if was slightly reversed after a wash-out of 1.5 h with drug-free solution. A second effect of the drug, the fast reinhibition, could be completely removed by wash-out. In summary if is inhibited by ZD 7288 at membrane potentials at which the virtual if gate is closed. Disinhibition occurs during long-lasting hyperpolarization but will hardly be operative in unclamped fibres under physiological conditions.

摘要

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本文引用的文献

1
VOLTAGE CLAMP TECHNIQUE IN MAMMALIAN CARDIAC FIBRES.哺乳动物心脏纤维中的电压钳技术。
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Use-dependent block of the pacemaker current I(f) in rabbit sinoatrial node cells by zatebradine (UL-FS 49). On the mode of action of sinus node inhibitors.扎替雷定(UL-FS 49)对家兔窦房结细胞起搏电流I(f)的使用依赖性阻滞。关于窦房结抑制剂的作用方式。
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Effects of the bradycardic agent ZD 7288 on membrane voltage and pacemaker current in sheep cardiac Purkinje fibres.
超极化激活阳离子通道中的阻滞剂状态依赖性和捕获:细胞内激活门控的证据
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Naunyn Schmiedebergs Arch Pharmacol. 1994 Dec;350(6):677-84. doi: 10.1007/BF00169374.
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Inhibitory actions of ZENECA ZD7288 on whole-cell hyperpolarization activated inward current (If) in guinea-pig dissociated sinoatrial node cells.先正达公司ZD7288对豚鼠离体窦房结细胞全细胞超极化激活内向电流(If)的抑制作用
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ICI D7288, a novel sinoatrial node modulator.ICI D7288,一种新型的窦房结调节剂。
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Pacemaker mechanisms in cardiac tissue.心脏组织中的起搏机制。
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7
Effects of Zeneca ZD7288 in comparison with alinidine and UL-FS 49 on guinea pig sinoatrial node and ventricular action potentials.与阿利尼定和UL-FS 49相比,捷利康ZD7288对豚鼠窦房结和心室动作电位的影响。
J Cardiovasc Pharmacol. 1994 Sep;24(3):380-7. doi: 10.1097/00005344-199409000-00005.
8
Inward current activated during hyperpolarization in the rabbit sinoatrial node cell.兔窦房结细胞超极化时激活的内向电流。
Pflugers Arch. 1980 May;385(1):11-9. doi: 10.1007/BF00583909.
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