Synergistic inhibitory effects of clopidogrel and rivaroxaban on platelet function and platelet-dependent thrombin generation in cats

被引:6
作者
Lo, Sara T. [1 ]
Li, Ronald H. L. [2 ]
Georges, Catherine J. [1 ]
Nguyen, Nghi [3 ]
Chen, Cheyenne K. [3 ]
Stuhlmann, Claire [1 ]
Oldach, Maureen Sigmund [4 ]
Rivas, Victor Noel [5 ]
Fousse, Samantha [6 ]
Harris, Samantha P. [7 ]
Stern, Joshua A. [8 ]
机构
[1] Univ Calif Davis, William R Prichard Vet Med Teaching Hosp, Sch Vet Med, Davis, CA USA
[2] Univ Calif Davis, Surg & Radiol Sci, Davis, CA 95616 USA
[3] Univ Calif Davis, Surg & Radiol Sci, Sch Vet Med, Davis, CA USA
[4] Univ Calif Davis, Med & Epidemiol, Davis, CA USA
[5] Univ Calif Davis, Med & Epidemiol, Sch Vet Med, Davis, CA USA
[6] Univ Calif Davis, Sch Vet Med VME, UC Davis 2108 Tupper Hall, One Shields Ave, Davis, CA 95616 USA
[7] Univ Arizona, Coll Med, Cellular & Mol Med, Tucson, AZ USA
[8] Univ Calif Davis, Dept Med & Epidemiol, 2108 Tupper Hall,One Shields Ave, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
cardiology; cardiovascular; clopidogrel resistance; factor Xa inhibitor; hypertrophic cardiomyopathy; saddle thrombus; thromboembolism; ARTERIAL THROMBOEMBOLISM; HYPERTROPHIC CARDIOMYOPATHY; PREVALENCE; ACTIVATION; ASPIRIN; ACID;
D O I
10.1111/jvim.16727
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
BackgroundDual antithrombotic treatment (DAT) with clopidogrel and rivaroxaban sometimes is prescribed to cats with hypertrophic cardiomyopathy at risk of thromboembolism. To date, no studies have evaluated their combined effects on platelet function. Objectives/HypothesisEvaluate the safety of DAT in healthy cats and compare, ex vivo, platelet-dependent thrombin generation and agonist-induced platelet activation and aggregation in cats treated with clopidogrel, rivaroxaban, or DAT. We hypothesized that DAT would safely modulate agonist-induced platelet activation and aggregation more effectively than single agent treatment. AnimalsNine apparently healthy 1-year-old cats selected from a research colony. MethodsUnblinded, nonrandomized ex vivo cross-over study. All cats received 7 days of rivaroxaban (0.6 +/- 0.1 mg/kg PO), clopidogrel (4.7 +/- 0.8 mg/kg PO), or DAT with defined washout periods between treatments. Before and after each treatment, adenosine diphosphate (ADP)- and thrombin-induced platelet P-selectin expression was evaluated using flow cytometry to assess platelet activation. Platelet-dependent thrombin generation was measured by fluorescence assay. Platelet aggregation was assessed using whole blood impedance platelet aggregometry. ResultsNo cats exhibited adverse effects. Of the 3 treatments, only DAT significantly decreased the number of activated platelets (P = .002), modulated platelet activation in response to thrombin (P = .01), dampened thrombin generation potential (P = .01), and delayed maximum reaction velocity (P = .004) in thrombin generation. Like clopidogrel, DAT inhibited ADP-mediated platelet aggregation. However, rivaroxaban alone resulted in increased aggregation and activation in response to ADP. Conclusion and Clinical ImportanceTreatment combining clopidogrel and rivaroxaban (DAT) safely decreases platelet activation, platelet response to agonists, and thrombin generation in feline platelets more effectively than monotherapy with either clopidogrel or rivaroxaban.
引用
收藏
页码:1390 / 1400
页数:11
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