生物活性 | |||
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描述 | Proteinase-activated receptors (PARs) represent a unique subclass of G-protein-coupled receptors of which four family members have now been cloned from a number of species[3]. PAR1 has been implicated as a key mediator in cellular functions and is activated by the PAR1 agonist, thrombin, as well as by serine proteases. TRAP-6 is a PAR1 agonist[2]. Adenosine 5′-diphosphate (ADP) inducible aggregation which is used to assess platelet response to thienopyridines was correlated to that by TRAP-6 (r = 0.33 to 0.72; p < 0.001 for all assays)[4]. In platelet-rich plasma (PRP) of patients (n = 34) with unexplained venous thromboembolism, platelet aggregometry was performed and the influence of TRAP-6 was determined. Compared to the control group, patients with venous thromboembolism showed an enhanced maximal platelet aggregation with low concentrations of TRAP-6 (2 μM)[5]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.34mL 0.27mL 0.13mL |
6.68mL 1.34mL 0.67mL |
13.35mL 2.67mL 1.34mL |
参考文献 |
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[3]International Union of Pharmacology. XXVIII. Proteinase-activated receptors |