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

Author:

Lo Sara T.1ORCID,Li Ronald H. L.2ORCID,Georges Catherine J.1,Nguyen Nghi3,Chen Cheyenne K.3,Stuhlmann Claire1,Oldach Maureen Sigmund4,Rivas Victor Noel5,Fousse Samantha6,Harris Samantha P.7,Stern Joshua A.8

Affiliation:

1. University of California Davis School of Veterinary Medicine William R. Prichard Veterinary Medical Teaching Hospital Davis California USA

2. Surgical and Radiological Sciences University of California, Davis Davis California USA

3. Surgical and Radiological Sciences University of California Davis School of Veterinary Medicine Davis California USA

4. Medicine and Epidemiology University of California, Davis Davis California USA

5. Medicine and Epidemiology University of California Davis School of Veterinary Medicine Davis California USA

6. University of California Davis School of Veterinary Medicine – VME, UC Davis 2108 Tupper Hall, One Shields Avenue Davis, California 95616‐5270 USA

7. Cellular and Molecular Medicine, College of Medicine University of Arizona Tucson Arizona USA

8. Department of Medicine & Epidemiology University of California, Davis, 2108 Tupper Hall, One Shields Avenue Davis, California 95616 USA

Abstract

AbstractBackgroundDual 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.

Funder

EveryCat Health Foundation

Publisher

Wiley

Subject

General Veterinary

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