Hunyady L, Sarkadi B, Cragoe E J, Spät A, Gárdos G
Department of Physiology, Semmelweis University of Medicine, Budapest, Hungary.
FEBS Lett. 1987 Dec 10;225(1-2):72-6. doi: 10.1016/0014-5793(87)81133-x.
Recently it has been suggested [(1987) Nature 325, 456-458; (1987) FEBS Lett. 212, 123-126] that the activation of Na+/H+ exchange is a prerequisite for platelet aggregation and the development of the Ca2+ signal. As direct evidence for the role of the Na+/H+-exchange pathway the inhibition of the Ca2+ signal by EIPA, a specific inhibitor of Na+/H+ exchange, was offered. Here we demonstrate that low concentrations of EIPA (below 1 microM) completely block Na+/H+ exchange while EIPA inhibits aggregation or Ca2+ mobilization only in concentrations 100-times greater than 1 microM. Moreover, another amiloride analogue, CBDMB, developed to act predominantly on Na+/Ca2+ exchange, does not affect Na+/H+ exchange in platelets but blocks aggregation and Ca2+ mobilization. We conclude that while Na+/H+ exchange has a fundamental role in platelet functions it is not prerequisite for the development of Ca2+ signal and aggregation.
最近有人提出[(1987)《自然》325, 456 - 458;(1987)《欧洲生物化学学会联合会快报》212, 123 - 126],钠/氢交换的激活是血小板聚集和钙信号产生的前提条件。作为钠/氢交换途径作用的直接证据,有人提出用钠/氢交换的特异性抑制剂EIPA抑制钙信号。在此我们证明,低浓度的EIPA(低于1微摩尔)能完全阻断钠/氢交换,而EIPA仅在浓度比1微摩尔高100倍时才抑制聚集或钙动员。此外,另一种主要作用于钠/钙交换的氨氯地平类似物CBDMB,并不影响血小板中的钠/氢交换,但能阻断聚集和钙动员。我们得出结论,虽然钠/氢交换在血小板功能中具有重要作用,但它不是钙信号产生和聚集的前提条件。