Bunazosin, an alpha-adrenoceptor antagonist, blocks calcium current in guinea-pig ventricular myocytes.

H Kotake, N Noguchi, S Matsuoka, I Hisatome, J Hasegawa, H Mashiba
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Abstract

1. Effect of bunazosin, an alpha 1-adrenoceptor antagonist, upon the slow inward Ca2+ current (ICa) was studied in single ventricular myocytes of the guinea-pig using a whole-cell patch-clamp technique. 2. Bunazosin (10-100 microM) decreased ICa in a concentration-dependent manner with an IC50 of 60 microM during depolarization to + 10 mV from the holding potential of -40 mV. 3. As for the inactivation process of ICa, the steady-state inactivation (f infinity) curve was shifted toward more negative potentials from -12 mV to -17 mV and -21 mV at f infinity = 0.5, by 30 microM and 70 microM bunazosin. 4. Inhibition of ICa by the compound (10 microM) was also dependent on stimulation frequency, with greater block induced at 2 Hz (50%) than at 0.33 Hz (13%). 5. It is concluded that bunazosin possesses a direct Ca2+ channel-blocking (class 4) action in a rate-dependent fashion.

Bunazosin,一种α -肾上腺素受体拮抗剂,阻断豚鼠心室肌细胞的钙电流。
1. 采用全细胞膜片钳技术研究了α 1-肾上腺素受体拮抗剂bunazosin对豚鼠单心室肌细胞缓慢内向Ca2+电流(ICa)的影响。2. Bunazosin(10-100微米)以浓度依赖的方式降低了ICa,在从-40毫伏保持电位到+ 10毫伏的去极化过程中,IC50为60微米。3.对于ICa的失活过程,在f_∞= 0.5,30微米和70微米的bunazosin作用下,稳态失活(f_∞)曲线从-12 mV向-17 mV和-21 mV的负电位方向移动。4. 该化合物(10微米)对ICa的抑制也依赖于刺激频率,2 Hz(50%)诱导的阻滞比0.33 Hz(13%)诱导的阻滞更大。5. 结论是,bunazosin以速率依赖的方式具有直接的Ca2+通道阻断(4类)作用。
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