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中国临床药理学与治疗学 ›› 2010, Vol. 15 ›› Issue (7): 732-736.

• 基础研究 • 上一篇    下一篇

替罗非班在体外对P-选择素、白介素-6、白介素-1β的影响

谢双锋1, 尹松梅1, 聂大年1, 李益清1, 肖洁1, 马丽萍1, 王秀菊1, 王景峰2   

  1. 1中山大学附属第二医院 血液内科, 2心内科,广州 510120,广东
  • 收稿日期:2010-03-04 修回日期:2010-06-24 出版日期:2010-07-26 发布日期:2020-09-15
  • 作者简介:谢双锋,男,博士,主治医师,研究方向:血栓病和血小板功能。Tel:020-81332486 E-mail:xiesf@163.com
  • 基金资助:
    广东省医学科研基金(B2007056)

Effect of tirofiban on the plasma inflammatory factors of P-selectin,IL-6 and IL-1β in vitro

XIE Shuang-feng1, YIN Song-mei1, NIE Da-nian1, LI Yi-qing1, XIAO Jie1, MA Li-ping1, WANG Xiu-ju1, WANG Jing-feng2   

  1. 1Department of Hematology, 2Department of Cardiology, Second Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510120, Guangdong, China
  • Received:2010-03-04 Revised:2010-06-24 Online:2010-07-26 Published:2020-09-15

摘要: 目的: 探讨血小板膜糖蛋白(GP)Ⅱb/Ⅲa受体拮抗剂替罗非班在体外对血浆炎症因子的影响,为合理应用血小板GPⅡb/Ⅲa受体拮抗剂提供理论依据。方法: 以二磷酸腺苷(ADP)或凝血酶为诱聚剂在体外激活血小板,同时加入20%、50%和80%抑制浓度的替罗非班,37 ℃共同孵育30 min,标本离心,取上清液用ELISA法检测P-选择素和IL-6、IL-1β等炎症因子的改变。结果: ADP(终浓度为 10 μmol/L)可诱导P-选择素增多;此效应能被31.25 μmol/L(IC20)以上浓度的替罗非班抑制;ADP对IL-6、IL-1β的产生无影响。凝血酶(终浓度 0.03 U/L)可诱导P-选择素、IL-6、IL-1β产生增多;此效应能被 156.25 μmol/L(IC50)以上浓度的替罗非班抑制。各浓度替罗非班单独应用对P-选择素、IL-6、IL-1β均无影响。结论: 替罗非班浓度在IC50以上时可抑制凝血酶诱导的P-选择素和炎症因子增多。充足剂量的替罗非班在体外有抑制血小板活化和炎症反应的双重效应。

关键词: 血小板, 替罗非班, 炎症因子

Abstract: AIM: To explore the anti-inflammatory effects of tirofiban in vitro, and to provide the theoretical basis for properly using the GP Ⅱb/Ⅲa receptor antagonists.METHODS: The platelets in the blood samples were activated in vitro with adenosine diphosphate (ADP) or thrombin respectively. Tirofiban was added to each sample in 20%, 50% or 80% inhibiting concentrations. Then the mixed liquor was incubated in 37 ℃ for 30 minutes. After centrifugation, the samples were divided to supernatants and sediments. The P-selectin, interleukin-6 (IL-6) and interleukin-1β (IL-1β) of were detected by enzyme linked immunosorbent assay (ELISA).RESULTS: ADP (final concentration: 10 μmol/L) could induce the production of P-selectin, that could be inhibited by tirofiban in concentrations higher than 31.25 μmol/L (IC20). ADP had no effect on the production of IL-6 or IL-1β. Thrombin (final concentration: 0.03 U/L) could induce the production of P-selectin, IL-6 and IL-1β, those could be inhibited by tirofiban in concentrations higher than 156.25 μmol/L (IC50). Tirofiban without ADP or thrombin had no effect on the production of P-selectin, IL-6 or IL-1β.CONCLUSION: Tirofiban in concentration higher than IC50 could inhibit the production of P-selectin and inflammatory factors induced by thrombin. Tirofiban in full dosage could inhibit the activation of platelet and decrease the production of inflammatory factors at the same time in vitro.

Key words: Platelet, Tirofiban, Inflammatory factor

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