Division of Cardiovascular Medicine, Department of Internal Medicine, The Ohio State University, 473 W. 12th Avenue, Suite 200, DHLRI, Columbus, OH 43210, USA.
J Thromb Thrombolysis. 2011 May;31(4):431-5. doi: 10.1007/s11239-010-0530-0.
BIIB 513 and EMD 85131 are selective inhibitors of the Na+/H+ exchanger-1 (NHE-1) that are benzoylguanidine derivatives of the clinically employed diuretic amiloride. Prior studies have suggested a role for NHE-1 activity in platelet activation and aggregation using amiloride or its non- benzoylguanidines derivatives. However, the concentrations employed in these prior studies were at levels known to exert effects on other ion transport systems besides the NHE-1. Therefore, the purpose of this study was to examine the effects of more selective NHE-1 inhibitors, BIIB 513 and EMD 85131, on platelet aggregation and in vivo cyclic flow following arterial injury. BIIB 513 and EMD 85131 effects on ex vivo canine and human platelet aggregation in response to various agents was monitored via platelet aggregation. For analysis of in vivo thrombus formation, a femoral artery crush injury model was employed and a flow meter was used to monitor the effect of BIIB 513 on cyclic blood flow. Treatment of either canine or human platelets with up to 1 mM of BIIB 513 had no effect on aggregation induced by platelet activating factor (PAF), thrombin receptor activator peptide (TRAP), or adenosine diphosphate (ADP). Additionally, the structurally related compound EMD 85131 at up to 1 mM failed to inhibit TRAP induced platelet aggregation. In vivo administration of up to 9 mg/kg of BIIB 513 intravenously failed to affect cyclic flow in a canine model of femoral artery injury. These data demonstrate that the specific and selective NHE-1 inhibitors BIIB 513 or EMD 85131 have no effect on ex vivo platelet aggregation or in vivo cyclic flow following arterial injury.
BIIB 513 和 EMD 85131 是 Na+/H+交换器-1(NHE-1)的选择性抑制剂,是临床上使用的利尿剂阿米洛利的苯甲酰胍衍生物。先前的研究表明,NHE-1 活性在血小板激活和聚集中起作用,使用阿米洛利或其非苯甲酰胍衍生物。然而,这些先前研究中使用的浓度水平已知会对除 NHE-1 以外的其他离子转运系统产生影响。因此,本研究的目的是研究更具选择性的 NHE-1 抑制剂 BIIB 513 和 EMD 85131 对血小板聚集和动脉损伤后体内循环的影响。通过血小板聚集监测 BIIB 513 和 EMD 85131 对犬和人血小板对各种药物反应的体外聚集的影响。为了分析体内血栓形成,采用股动脉挤压损伤模型,使用流量计监测 BIIB 513 对循环血流的影响。高达 1mM 的 BIIB 513 处理犬或人血小板对血小板激活因子(PAF)、血栓素受体激活肽(TRAP)或二磷酸腺苷(ADP)诱导的聚集没有影响。此外,高达 1mM 的结构相关化合物 EMD 85131 也不能抑制 TRAP 诱导的血小板聚集。静脉内给予高达 9mg/kg 的 BIIB 513 不会影响股动脉损伤犬模型中的循环流量。这些数据表明,特异性和选择性 NHE-1 抑制剂 BIIB 513 或 EMD 85131 对体外血小板聚集或动脉损伤后体内循环没有影响。