Synergistic inhibitory effects of clopidogrel and rivaroxaban on platelet function and platelet-dependent thrombin generation in cats
Author
Lo, S.T.Li, R.H.L.
Georges, C.J.
Nguyen, N.
Chen, C.K.
Stuhlmann, C.
Oldach, M.S.
Rivas, V.N.
Fousse, S.
Harris, S.P.
Stern, J.A.
Affiliation
Cellular and Molecular Medicine, College of Medicine, University of ArizonaIssue Date
2023-05-19Keywords
cardiologycardiovascular
clopidogrel resistance
factor Xa inhibitor
hypertrophic cardiomyopathy
saddle thrombus
thromboembolism
Metadata
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John Wiley and Sons IncCitation
Lo ST, Li RHL, Georges CJ, et al. Synergistic inhibitory effects of clopidogrel and rivaroxaban on platelet function and platelet-dependent thrombin generation in cats. J Vet Intern Med. 2023; 37(4): 1390-1400. doi:10.1111/jvim.16727Rights
© 2023 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC on behalf of American College of Veterinary Internal Medicine. This is an open access article under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Background: Dual 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/Hypothesis: Evaluate 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. Animals: Nine apparently healthy 1-year-old cats selected from a research colony. Methods: Unblinded, 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. Results: No 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 Importance: Treatment 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. © 2023 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC on behalf of American College of Veterinary Internal Medicine.Note
Open access journalISSN
0891-6640PubMed ID
37208839Version
Final Published Versionae974a485f413a2113503eed53cd6c53
10.1111/jvim.16727
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Except where otherwise noted, this item's license is described as © 2023 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC on behalf of American College of Veterinary Internal Medicine. This is an open access article under the terms of the Creative Commons Attribution License.
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