Kalinowski Leszek, Matys Tomasz, Chabielska Ewa, Buczko Włodzimierz, Malinski Tadeusz
Department of Chemistry and Biochemistry, Ohio University, Athens, Ohio 45701, USA.
Hypertension. 2002 Oct;40(4):521-7. doi: 10.1161/01.hyp.0000034745.98129.ec.
This study investigated the process of nitric oxide (NO) release from platelets after stimulation with different angiotensin II type 1 (AT1)-receptor antagonists and its effect on platelet adhesion and aggregation. Angiotensin II AT1-receptor antagonist-stimulated NO release in platelets was compared with that in human umbilical vein endothelial cells by using a highly sensitive porphyrinic microsensor. In vitro and ex vivo effects of angiotensin II AT1-receptor antagonists on platelet adhesion to collagen and thromboxane A2 analog U46619-induced aggregation were evaluated. Losartan, EXP3174, and valsartan alone caused NO release from platelets and endothelial cells in a dose-dependent manner in the range of 0.01 to 100 micro mol/L, which was attenuated by NO synthase inhibitor N(G)-nitro-L-arginine methyl ester. The angiotensin II AT1-receptor antagonists had more than 70% greater potency in NO release in platelets than in endothelial cells. The degree of inhibition of platelet adhesion (collagen-stimulated) and aggregation (U46619-stimulated) elicited by losartan, EXP3174, and valsartan, either in vitro or ex vivo, closely correlated with the NO levels produced by each of these drugs alone. The inhibiting effects of angiotensin II AT1-receptor antagonists on collagen-stimulated adhesion and U46619-stimulated aggregation of platelets were significantly reduced by pretreatment with N(G)-nitro-L-arginine methyl ester. Neither the AT2 receptor antagonist PD123319, the cyclooxygenase synthase inhibitor indomethacin, nor the selective thromboxane A2/prostaglandin H2 receptor antagonist SQ29,548 had any effect on angiotensin II AT1-receptor antagonist-stimulated NO release in platelets and endothelial cells. The presented studies clearly indicate a crucial role of NO in the arterial antithrombotic effects of angiotensin II AT1-receptor antagonists.
本研究调查了不同的1型血管紧张素II(AT1)受体拮抗剂刺激后血小板释放一氧化氮(NO)的过程及其对血小板黏附和聚集的影响。通过使用高灵敏度卟啉微传感器,将血管紧张素II AT1受体拮抗剂刺激血小板释放NO的情况与人脐静脉内皮细胞进行了比较。评估了血管紧张素II AT1受体拮抗剂对血小板黏附于胶原蛋白以及血栓素A2类似物U46619诱导的聚集的体外和体内效应。氯沙坦、EXP3174和缬沙坦单独使用时,在0.01至100微摩尔/升范围内以剂量依赖方式引起血小板和内皮细胞释放NO,这一过程被一氧化氮合酶抑制剂N(G)-硝基-L-精氨酸甲酯减弱。血管紧张素II AT1受体拮抗剂在血小板中释放NO的效力比在内皮细胞中高70%以上。氯沙坦、EXP3174和缬沙坦在体外或体内对血小板黏附(胶原蛋白刺激)和聚集(U46619刺激)的抑制程度与这些药物单独产生的NO水平密切相关。用N(G)-硝基-L-精氨酸甲酯预处理可显著降低血管紧张素II AT1受体拮抗剂对胶原蛋白刺激的血小板黏附和U46619刺激的血小板聚集的抑制作用。2型血管紧张素受体拮抗剂PD123319、环氧化酶合酶抑制剂吲哚美辛以及选择性血栓素A2/前列腺素H2受体拮抗剂SQ29548对血管紧张素II AT1受体拮抗剂刺激血小板和内皮细胞释放NO均无影响。所呈现的研究清楚地表明NO在血管紧张素II AT1受体拮抗剂的动脉抗血栓作用中起关键作用。