Rabkin S W
University of British Columbia, Vancouver, Canada.
Tissue Cell. 1996 Aug;28(4):469-72. doi: 10.1016/s0040-8166(96)80032-2.
We have previously shown that indapamide [chloro-4-N-(methyl-2-indolinyl-1)-sulfamoyal-3-benzamide] has a direct action on the heart to alter ion fluxes. This study sought to examine the potential interaction between indapamide and epidermal growth factor (EGF). Cardiomyocytes were prepared as primary culture from 7-day-old chick embryo hearts as aggregates that have a pattern of consistent spontaneous contraction. Indapamide enhanced the positive chronotropic response to EGF observed in chick embryonic ventricular myocyte aggregates while indapamide itself did not alter cardiac contractile frequency. Taken in conjunction with data that calcium channel blockade, inhibition of sodium entry or Na(+)-Ca2+ exchange in the cardiomyocyte opposes the positive chronotropic action of EGF on the cardiomyocyte, this study has identified an agent, indapamide, that accentuates the cardiomyocyte response to EGF.
我们之前已经表明,吲达帕胺[4-氯-N-(甲基-2-吲哚啉-1)-磺酰胺基-3-苯甲酰胺]对心脏有直接作用,可改变离子通量。本研究旨在探讨吲达帕胺与表皮生长因子(EGF)之间的潜在相互作用。从7日龄鸡胚心脏制备原代培养的心肌细胞聚集体,这些聚集体具有一致的自发收缩模式。吲达帕胺增强了鸡胚心室肌细胞聚集体中观察到的对EGF的正性变时反应,而吲达帕胺本身并未改变心脏收缩频率。结合心肌细胞中钙通道阻滞、钠内流抑制或钠钙交换抑制会对抗EGF对心肌细胞的正性变时作用的数据,本研究确定了一种药物吲达帕胺,它可增强心肌细胞对EGF的反应。