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Isolation and Culture of Primary Endothelial Cells from Canine Arteries and Veins
Published on: November 18, 2016
Platelet cyclooxygenase expression in normal dogs.
J Thomason1, K Lunsford, K Mullins
1Department of Clinical Sciences, Mississippi State University, Mississippi State, MS 39762-6100, USA. thomason@cvm.msstate.edu
Journal of Veterinary Internal Medicine
|October 12, 2011
Summary
Canine platelets express cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2). Aspirin increased COX-1 expression and impaired platelet function, while COX-2 expression varied significantly among dogs.
Area of Science:
- Veterinary Medicine
- Pharmacology
- Biochemistry
Background:
- Human platelets express cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2).
- Variations in COX-2 expression may explain differing responses to aspirin therapy.
Purpose of the Study:
- To determine if circulating canine platelets express COX-1 and COX-2.
- To investigate how aspirin administration affects COX expression and platelet function in dogs.
Main Methods:
- Eight intact female hounds were studied using a repeated measures design.
- Platelet COX-1 and COX-2 expression were measured by flow cytometry before and after 10 days of aspirin (10 mg/kg Q12h).
- Platelet function was assessed using PFA-100(®) (collagen/epinephrine), and urine 11-dehydro-thromboxane B(2) (11-dTXB(2)) to creatinine ratio was measured.
Main Results:
- Both COX-1 and COX-2 were detected in canine platelets.
- Aspirin administration led to a 250% increase in COX-1 expression in all dogs.
- COX-2 expression showed significant inter-individual variation and did not change significantly after aspirin; platelet function was impaired, and urine 11-dTXB(2) decreased in all dogs.
Conclusions:
- Canine platelets express both COX-1 and COX-2 isoforms.
- Aspirin increases COX-1 expression and impairs platelet function, but COX-2 expression varies considerably among dogs.
- Inter-individual variability in platelet COX-2 expression warrants further investigation as a potential marker for variable aspirin responsiveness.
