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佛波酯对豚鼠离体心脏组织收缩力、动作电位和钙电流的影响。

Influence of phorbol esters on contractile force, action potential and calcium current of isolated guinea-pig heart tissues.

作者信息

Siems T, Brasch H

机构信息

Institut für Pharmakologie Medizinische Universität zu Lübeck, FRG.

出版信息

Basic Res Cardiol. 1995 Nov-Dec;90(6):459-66. doi: 10.1007/BF00788538.

Abstract

Phorbol-12, 13-dibutyrate (PDB) reduced concentration-dependently the contractile force of guinea-pig papillary muscles (EC50 1.07 mumol/l) while phorbol-12-myristate-13-acetate (PMA) was ineffective. The protein kinase C inhibitors staurosporine (0.1 mumol/l) and polymyxin B (70 mumol/l) did not antagonize the negative inotropic effect of PDB. Neither PMA nor PDB, in concentrations up to 30 mumol/l, caused significant changes of the maximum depolarization velocity, the action potential duration or the functional refractory period in intact papillary muscles. In isolated ventricular cardiomyocytes the inward calcium current was halved by either 1 mumol/l PDB or 10 mumol/1 PMA. PKC inhibitors attenuated, but could not completely abolish this effect of the phorboles. It is concluded that the negative inotropic effect of PDB is caused by a reduction of the slow inward calcium current and that this inhibition is, for the greater part, not mediated by an activation of protein kinase C.

摘要

佛波醇 -12,13 - 二丁酸酯(PDB)浓度依赖性地降低豚鼠乳头肌的收缩力(半数有效浓度为1.07μmol/L),而佛波醇 -12 - 肉豆蔻酸酯 -13 - 乙酸酯(PMA)则无此作用。蛋白激酶C抑制剂星形孢菌素(0.1μmol/L)和多粘菌素B(70μmol/L)不能拮抗PDB的负性肌力作用。浓度高达30μmol/L的PMA和PDB均未引起完整乳头肌的最大去极化速度、动作电位持续时间或功能不应期发生显著变化。在离体心室心肌细胞中,1μmol/L的PDB或10μmol/L的PMA均可使内向钙电流减半。蛋白激酶C抑制剂可减弱但不能完全消除佛波醇的这种作用。结论是,PDB的负性肌力作用是由缓慢内向钙电流减少所致,且这种抑制作用在很大程度上并非由蛋白激酶C的激活介导。

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