Samson J, Stelmach H, Tomasiak M
Department of Physical Chemistry, Medical Academy of Bialystok, Mickiewicza 2A, 15-230 Bialystok, Poland.
Platelets. 2001 Nov;12(7):436-42. doi: 10.1080/09537100120078395.
This study addresses the role of the Na+/H+ exchanger (NHE) in the generation of procoagulant activity in blood platelets. It was found that monensin (simulating the action of NHE) and gramicidin (causing sodium influx without concomitant H+ efflux) produced a dose- and time-dependent increase in platelet procoagulant activity. Alkalinization of platelet cytosol by NH(4)Cl failed to evoke a procoagulant response. Collagen-induced procoagulant response was diminished in the absence of external Na+ and in the presence of EIPA (NHE inhibitor) or GF 109203X (protein kinase C inhibitor). Phorbol ester (PMA) produced a dose- and time-dependent generation of procoagulant response which was inhibited in the absence of the external Na+ and in the presence of EIPA. Platelets stimulated by collagen and PMA accumulated (22)Na+, a phenomenon inhibited in the presence of EIPA. The data indicate that development of procoagulant activity in platelets may occur as a result of Na+ influx via Na+/H+ exchanger.
本研究探讨了钠氢交换体(NHE)在血小板促凝血活性产生中的作用。研究发现,莫能菌素(模拟NHE的作用)和短杆菌肽(导致钠内流但无伴随的氢外流)可使血小板促凝血活性呈剂量和时间依赖性增加。氯化铵使血小板胞质碱化未能引发促凝血反应。在无细胞外钠以及存在EIPA(NHE抑制剂)或GF 109203X(蛋白激酶C抑制剂)的情况下,胶原蛋白诱导的促凝血反应减弱。佛波酯(PMA)可产生剂量和时间依赖性的促凝血反应,在无细胞外钠以及存在EIPA的情况下该反应受到抑制。胶原蛋白和PMA刺激的血小板积累了22Na +,在存在EIPA的情况下这种现象受到抑制。数据表明,血小板促凝血活性的产生可能是由于通过钠氢交换体的钠内流所致。