دورية أكاديمية

Effect of alteplase on platelet function and receptor expression

التفاصيل البيبلوغرافية
العنوان: Effect of alteplase on platelet function and receptor expression
المؤلفون: Jun Lu, Peng Hu, Guangyu Wei, Qi Luo, Jianlin Qiao, Deqin Geng
المصدر: Journal of International Medical Research, Vol 47 (2019)
بيانات النشر: SAGE Publishing, 2019.
سنة النشر: 2019
المجموعة: LCC:Medicine (General)
مصطلحات موضوعية: Medicine (General), R5-920
الوصف: Objective To investigate the role of alteplase, a widely-used thrombolytic drug, in platelet function. Methods Human platelets were incubated with different concentrations of alteplase followed by analysis of platelet aggregation in response to adenosine diphosphate (ADP), collagen, ristocetin, arachidonic acid or epinephrine using light transmittance aggregometry. Platelet activation and surface levels of platelet receptors GPIbα, GPVI and αIIbβ3 were analysed using flow cytometry. The effect of alteplase on clot retraction was also examined. Results This study demonstrated that alteplase significantly inhibited platelet aggregation in response to ADP, collagen and epinephrine in a dose-dependent manner, but it did not affect ristocetin- or arachidonic acid-induced platelet aggregation. Alteplase did not affect platelet activation as demonstrated by no differences in P-selectin levels and PAC-1 binding being observed in collagen-stimulated platelets after alteplase treatment compared with vehicle. There were no changes in the surface levels of the platelet receptors GPIbα, GPVI and αIIbβ3 in alteplase-treated platelets. Alteplase treatment reduced thrombin-mediated clot retraction. Conclusions Alteplase inhibits platelet aggregation and clot retraction without affecting platelet activation and surface receptor levels.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0300-0605
1473-2300
03000605
Relation: https://doaj.org/toc/0300-0605; https://doaj.org/toc/1473-2300
DOI: 10.1177/0300060519829991
URL الوصول: https://doaj.org/article/5559caf555cc4c3a8fbd5eb8ab81a6ed
رقم الأكسشن: edsdoj.5559caf555cc4c3a8fbd5eb8ab81a6ed
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:03000605
14732300
DOI:10.1177/0300060519829991