Blockade of bepridil on IA and IK in acutely isolated hippocampal CA1 neurons

被引:13
作者
Hu, HJ [1 ]
Yang, DM
Lin, ZJ
Wu, CH
Zhou, PA
Dai, DZ
机构
[1] China Pharmaceut Univ, Dept Pharmacol Chinese Mat Med, Nanjing 21009, Peoples R China
[2] Peking Univ, Natl Lab Biomembrane & Membrane Biotechnol, Beijing 100871, Peoples R China
[3] China Pharmaceut Univ, Res Div Pharmacol, Nanjing 21009, Peoples R China
关键词
hippocampus; CA1; neuron; patch-clamp; bepridil; potassium current;
D O I
10.1016/S0006-8993(98)00815-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of bepridil, an antianginal agent with antiarrhythmic action, on voltage-dependent K+ currents in the CA1 pyramidal neurons acutely isolated from rat hippocampus were studied by means of whole-cell patch clamp techniques. Current recordings were made in the presence of TTX to block Na+ current. Depolarizing test pulses activated two components of outward K+ currents: a rapidly activating and inactivating component, I-A; and a delayed component, I-K. Results showed that bepridil reduced the amplitude of I, and I-K, and exerted its inhibitory action in time- and dose-dependent manner. Half-blocking concentrations (IC50) of bepridil on I-A and I-K were 17.8 mu M and 1.7 mu M, respectively. 10 mu M bepridil suppressed I-A and I-K by 46.7% and 77.1% at +30 mV of depolarization, respectively. When I-K was activated nearly uncontaminated with I-A by holding at -50 mV, 10 mu M bepridil inhibited I-K by 71.6% at +30 mV of depolarization; 10 mu M bepridil positively shifted the voltage-dependent of activation curves of I-A and I-K 12.1 mV and 28.7 mV, respectively. These results suggested that blockade on K+ currents by bepridil is preferential for I-K, and contributes to the protection brain against ischemic damage. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 154
页数:6
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