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托博林酮对兔和豚鼠离体心脏的正性肌力和变时作用及其电生理特性

Positive inotropic and chronotropic effects of toborinone and its electrophysiological properties in the isolated hearts of rabbits and guinea-pigs.

作者信息

Takase H, Orito K, Mori T, Fujiki H, Sekiguchi K, Tominaga M, Iijima T

机构信息

2nd Tokushima Institute of New Drug Research, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.

出版信息

Arzneimittelforschung. 1996 Jun;46(6):579-86.

PMID:8767347
Abstract

The inotropic and chronotropic actions of toborinone ((+/-)-6-[3-(3,4-dimethoxybenzylamino)-2-hydroxy-propoxy]-2(1H)-qu inolinone CAS 128667-95-8, OPC-18790) in the isolated right atrial and papillary muscles of rabbit and guinea-pig were examined and compared with those of milrinone (CAS 78415-72-2), a pure cyclic GMP-inhibited phosphodiesterase inhibitor. OPC-18790 (10(-7)-10(-4) mol/l) and milrinone (10(-3)-10(-4) mol/l) exerted concentration-dependent increases of contraction in both atrial and papillary muscles isolated from rabbits and guinea-pigs. In the isolated right atrium of rabbits and guinea-pigs, OPC-18790 showed limited increase in heart rate, while milrinone increased heart rate concentration-dependently. OPC-18790 (10(-6) and 10(-5) mol/l in guinea-pigs and 10(-7)-10(-4) mol/l in rabbits) prolonged the action potential duration in the isolated papillary muscles, while milrinone exerted no such change. In whole-cell voltage clamp experiments using isolated cardiac myocytes of guinea-pigs, OPC-18790(10(-5) mol/l) increased the L-type calcium current and inhibited outward potassium currents such as inward rectifying currents and delayed rectifier currents. OPC-18790 and milrinone (10(-6), 3 x 10(-5) mol/l) increased intracellular cyclic AMP levels with an increase in developed tension in isolated right ventricular muscles of guinea-pigs. From the above results, OPC-18790 was shown to be a positive inotropic agent with limited chronotropic effect and electrophysiologically properties different from those of milrinone. It was suggested that the prolongation of action potential duration, which is due to the inhibition of potassium currents, may be involved in OPC-18790's mechanism of positive inotropic action with limited chronotropic effect in addition to the inhibition of cyclic GMP-inhibited phosphodiesterase.

摘要

研究了托波律酮((±)-6-[3-(3,4-二甲氧基苄基氨基)-2-羟基-丙氧基]-2(1H)-喹啉酮,CAS 128667-95-8,OPC-18790)对兔和豚鼠离体右心房及乳头肌的变力性和变时性作用,并与米力农(CAS 78415-72-2)进行比较,米力农是一种纯的环鸟苷酸抑制性磷酸二酯酶抑制剂。OPC-18790(10⁻⁷ - 10⁻⁴ mol/L)和米力农(10⁻³ - 10⁻⁴ mol/L)使兔和豚鼠离体心房和乳头肌的收缩呈浓度依赖性增加。在兔和豚鼠的离体右心房中,OPC-18790使心率增加有限,而米力农使心率呈浓度依赖性增加。OPC-18790(豚鼠为10⁻⁶和10⁻⁵ mol/L,兔为10⁻⁷ - 10⁻⁴ mol/L)使离体乳头肌的动作电位时程延长,而米力农无此变化。在使用豚鼠离体心肌细胞的全细胞电压钳实验中,OPC-18790(10⁻⁵ mol/L)增加L型钙电流并抑制外向钾电流,如内向整流电流和延迟整流电流。OPC-18790和米力农(10⁻⁶、3×10⁻⁵ mol/L)使豚鼠离体右心室肌细胞内环磷酸腺苷水平升高,同时张力增加。根据上述结果,OPC-18790是一种正性肌力药物,变时作用有限,电生理特性与米力农不同。提示动作电位时程的延长可能与OPC-18790正性肌力作用且变时作用有限的机制有关,这一延长是由于钾电流受抑制所致,此外还与环鸟苷酸抑制性磷酸二酯酶的抑制有关。

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