Phosphodiesterase isoenzymes in equine platelets and their influence on platelet adhesion.
Abstract: To determine the phosphodiesterase (PDE) isoenzymes in equine platelets and evaluate their influence on platelet adhesion. Methods: Platelets obtained from healthy New Forest Pony geldings that ranged from 12 to 20 years of age (mean +/- SEM, 17.3 +/- 1.1 years). Methods: PDE isoenzyme activity in equine platelets was determined by use of a 2-step radioactive assay. Functional importance of PDE isoenzymes was established by use of selective inhibitors in a colorimetric adhesion assay. Results: PDE1, PDE2, PDE3, and PDE5 and small amounts of PDE4 were found in equine platelets. Inhibition of PDE3 abolished platelet adhesion almost completely, whereas inhibition of PDE4 and PDE5 had little effect. Conclusions: Function of equine platelets can be influenced by inhibition of PDE3. Selective PDE3 inhibitors may be clinically useful to regulate platelet function. They offer the advantage of increased potency with fewer adverse effects, compared with those for nonselective PDE inhibitors.
Publication Date: 2007-12-07 PubMed ID: 18052741DOI: 10.2460/ajvr.68.12.1354Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research explores the presence of phosphodiesterase isoenzymes in the blood platelets of horses and their effect on platelet adherence. The study finds that these isoenzymes can influence platelet function, and that specially targeting PDE3 could be beneficial in controlling platelet activity.
Overview of The Study
- The study focuses on phosphodiesterase isoenzymes (PDE), particularly in the platelets of equine species.
- Phosphodiesterase isoenzymes are a group of enzymes that function in diverse biological pathways.
- The platelets used in the study were drawn from healthy New Forest Pony geldings — male horses aged between 12 and 20 years.
Determination of Isoenzyme Activity
- The activity of PDE isoenzymes in the platelets was measured using a 2-step radioactive assay, a process employed in detecting and measuring the quantity of a particular substance.
- PDE1, PDE2, PDE3, PDE5, and small amounts of PDE4 enzymes were found.
The Role of Isoenzymes in Platelet Adhesion
- The researchers further studied the impact of these PDE isoenzymes on the propensity of platelets to adhere or stick together.
- The significance of these enzymes was established using selective inhibitors in a colorimetric adhesion assay, a test that measures the degree of attachment.
- The study showed that inhibiting PDE3 almost completely eradicated platelet adhesion, whereas preventing PDE4 and PDE5 had a lesser effect.
Conclusions and Implications
- The ability of equine platelets to function can be influenced by inhibiting PDE3, suggesting that selective PDE3 inhibitors could be used to control platelet activity.
- The researchers propose that these inhibitors could provide a stronger effect with fewer adverse impacts compared to nonselective PDE inhibitors. This hypothesis may have implications for medical applications, opening up new avenues for controlling and preventing blood clotting disorders in horses.
Cite This Article
APA
Dunkel B, Rickards KJ, Page CP, Cunningham FM.
(2007).
Phosphodiesterase isoenzymes in equine platelets and their influence on platelet adhesion.
Am J Vet Res, 68(12), 1354-1360.
https://doi.org/10.2460/ajvr.68.12.1354 Publication
Researcher Affiliations
- Department of Veterinary Basic Sciences, The Royal Veterinary College, North Mymms, Herts, England.
MeSH Terms
- Animals
- Blood Platelets / drug effects
- Blood Platelets / enzymology
- Cell Adhesion / physiology
- Cells, Cultured
- Dose Fractionation, Radiation
- Horses / blood
- Isoenzymes / metabolism
- Male
- Phosphoric Diester Hydrolases / metabolism
- Platelet Aggregation Inhibitors / pharmacology
Citations
This article has been cited 1 times.- Stokol T, Serpa PBS, Zahid MN, Brooks MB. Unfractionated and Low-Molecular-Weight Heparin and the Phosphodiesterase Inhibitors, IBMX and Cilostazol, Block Ex Vivo Equid Herpesvirus Type-1-Induced Platelet Activation. Front Vet Sci 2016;3:99.
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