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Comparative study of two prostaglandins inhibiting adenosine diphosphate-induced platelet aggregation in vitro |
XIA Qing1, LI Yi2, LI Wei1, HU Huijing2, CHEN Yun2, RUAN Jingxiong3 |
1. Department of Pharmacy, Air Force No.986 Hospital,Xi’an 710054,China; 2.Xi’an Libang Zhaoxin Biotechnology Limited Company,Xi’an 710077,China; 3. Department of Clinical Laboratory, the First Affiliated Hospital of Xi’an Jiaotong University,Xi’an 710061,China |
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Abstract ObjectiveTo investigate the inhibitory effects of two types of prostaglandins(epoprostenol sodium and prostaglandin E1) on adenosine diphosphate (ADP)-induced platelet aggregation in vitro.Methods Platelet suspension was incubated with epoprostenol sodium and prostaglandin E1 respectively at different concentrations(0, 50, 125, 500 and 2500 ng/ml)before the maximal extent of platelet aggregation was determined at the best ADP concentration and the best incubation time.Results At 20 μM ADP and after incubation of 5 min, the platelet aggregation of both types of prostaglandins induced by ADP was reduced accordingly with the increase of the concentrations of epoprostenol sodium and prostaglandin E1. The inhibitory rate of platelet aggregation induced by epoprostenol sodium was 19.61%, 48.13%, 88.25%, 93.71%, and 100% respectively,compared with 5.20%, 11.70%, 23.16%, 28.10% and 65.09% respectively for prostaglandin E1.Conclusions Epoprostenol sodium and prostaglandin E1 can inhibit ADP-induced platelet aggregation in a concentration-dependent manner in vitro, and the former is more effective.
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Received: 02 June 2019
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[1] |
Weiss H J, Turitto V T. Prostacyclin (Prostaglandin I2, PGI2) inhibits plat-elet adhesion and thrombus formation on subendothelium[J], Blood, 1979, 53(2): 244-250.
|
[2] |
O’Connell C, Amar D, Boucly A, et al. Comparative safety and tolerability of prostacyclins in pulmonary hypertension[J], Drug Saf, 2016, 39(4): 287-294.
|
[3] |
Akagi S, Nakamura K, Matsubara H, et al. Epoprostenol therapy for pulm-onary arterial hypertension[J], Acta Med Okayama, 2015, 69(3): 129-136.
|
[4] |
Chin K M, Badesch D B, Robbins I M, et al. Two formulations of epoprostenol sodium in the trea tment of pulmonary arterial hypertension: PITOME-1 (epoprostenol for injection in pulmonary arterial hypertension), aphase Ⅳ, open-label, randomized study[J]. Am Heart J, 2014, 167(2): 218-225.
|
[5] |
王 琳.前列地尔联合甲钴胺治疗糖尿病视网膜病变临床疗效观察[J].临床合理用药,2018, 11(3): 58-59.
|
[6] |
周俊江.探讨前列地尔治疗突发性耳聋的临床应用价值[J]. 江西医药, 2013, 48(12): 1261-1262.
|
[7] |
樊华英,李慧娟,韩俊霞. 前列地尔联合厄贝沙坦治疗对老年糖尿病肾病患者蛋白尿、hs-CRP的效果分析[J]. 中国现代药物应用,2018,12(22): 126-127.
|
[8] |
江思德,肖 静,邹耀兵,等. 前列地尔注射液治疗急性脑梗死44例临床疗效研究[J]. 中国药业, 2015, 24(24):31-32.
|
[9] |
李珊珊.硫辛酸与前列地尔联合治疗糖尿病早期微血管病变的临床观察[J]. 药物研究, 2016, (7):78.
|
[10] |
傅桥菲, 陈春林. 前列地尔治疗高血压视网膜病变的临床研究[J].江西医药, 2018, 53(11): 1321-1323.
|
[11] |
方淑贤,郑 恒,刘 东,等. 穿心莲内酯对二磷酸腺苷诱导血小板聚集的拮抗作用[J]. 医药导报, 2004 23(11):805-806.
|
[12] |
但 刚, 罗鸿雁, 江忠勇,等. 不同血小板浓度对血小板聚集率的影响探讨[J]. 西南国防医药, 2016, 26(8):832-834.
|
[13] |
林兆瑛.血小板聚集素(TXA_2)和前列腺环素(PGI_2)[J]. 四川生理科学动态, 1983 (1):9-15.
|
[14] |
Fred V, Victor A, Skrinska, et al. Stability of prostacyclin in human and rabbit whole blood and plasa[J], Thromab Res, 1986,43:379-387.
|
[15] |
内阁莱什.R.帕莱普. 新颖的依前列醇制剂及其制备方法[P].中国专利,公开号:CN 101410119.
|
[16] |
Madelene Lindkvist,Ulrika Fernberg,Liza U. Individual variations in platelet reactivity towards ADP, epinephrine, collagen and nitric oxide, and the association to arterial function in young, healthy adults[J]. Thromb Res, 2019, 174: 5-12.
|
[17] |
翟 婷,华声瑜. 血小板ADP受体及其拮抗剂的研究进展[J]. 天津中医药, 2017, 34(4):280-284.
|
|
|
|